Gastric VaricesPRADANCT07168395
Pre-emptive RTO for An Early Detected Gastric Varices in CT/MR Angiogram Trial
A study testing Non-selective beta blockers and Retrograde transvenous obliteration in people with Gastric Varices, run by University of California, Los Angeles.
Trial summary
A number of treatment modalities are currently in use for gastric variceal bleeding (GVB). Balloon-occluded, plug-assisted, and coil-assisted retrograde transvenous obliteration (RTO) procedures are described in the literature as treatments for GVB after a bleeding episode occurs. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Gastric Varices
- What is being tested?
- Non-selective beta blockers and Retrograde transvenous obliteration
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 68 participants
- Where
- No sites listed yet
- Study dates
- Oct 2026to Nov 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age > 18 years
- Patients with compensated cirrhosis with a higher risk of decompensation based on AASLD 2023 Practice Guidance (Kaplan et al) - no ascites with endoscopic visualization of varices
- Confirmed diagnosis of gastric varices either through CT, MRI, or Endoscopy.
- No imaging (LIRAD4 or 5) or tumor marker (AFP) evidence of HCC or other malignancy
- MELD < 20
- First de novo RTO procedure
Show all 11Show fewer
- Taking NSBB
- Patent internal jugular or right common femoral vein
- Willing to provide the hepatology service information for F/U
- No known diagnosis of hypercoagulopathy
- Patent portal vein or portal vein cavernous transformation
Who cannot join
- Age <18 years
- Patients with decompensated cirrhosis based on AASLD 2023 Practice Guidance (Kaplan et al)
- Cardiac failure
- Active variceal bleeding
- History of gastroesophageal variceal bleeding
- Previous TIPS, BRTO, CARTO or PARTO procedure
Show all 10Show fewer
- No right jugular or right common femoral venous access
- No portal vein flow
- Malignancy
- Life expectancy of less than 6 months
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Pre-emptive RTO for An Early Detected Gastric Varices in CT/MR Angiogram Trial (PRADA Trial)
A number of treatment modalities are currently in use for gastric variceal bleeding (GVB). Balloon-occluded, plug-assisted, and coil-assisted retrograde transvenous obliteration (RTO) procedures are described in the literature as treatments for GVB after a bleeding episode occurs. Preliminary data suggests that prophylactic treatment of gastric varices may improve patient outcomes compared to conservative management. This study aims to compare pre-emptive treatment of gastric varices with current recommended medical management in a randomized prospective study design. Eligible patients will be randomized to receive RTO or to continue conservative management. Patients will be followed for up to 2 years for comparison of clinical outcomes, including episodes of gastric variceal bleeding, overall survival and transplant-free survival, complications, and secondary interventions.
Read the detailed description
Gastroesophageal varices occur in approximately 50% of patients with liver cirrhosis. Specifically, gastric varices (GV) are responsible for roughly 10-30% of all variceal hemorrhage which is less than their counterpart esophageal varices. Despite their lower recurrence rates, gastric variceal bleeds (GVB) are associated with higher mortality, with an estimated 35-90% of patients developing rebleeding after achieving hemostasis.
Currently, there are several treatments for GVB that include endoscopic injection therapies, percutaneous antegrade transhepatic obliteration (ATO), transjugular portosystemic shunt placement (TIPS), splenic artery embolization (SAE), and surgical treatment. However, these procedures in previously studied trials have well-documented risks that compromise clinical outcomes. One specific interventional radiology procedure that has maintained a positive reputation in its use for gastric variceal bleeds is balloon-occluded retrograde transvenous obliteration (BRTO). This was first reported by Kanagawa et al. in the early 1990s; BRTO remains a well-accepted method of treatment of gastric fundal varices with gastrorenal or gastrophrenic shunts because of its minimally invasive nature and highly effective results, with studies showing up to 95% clinical success rate in stopping variceal bleeding. However, this procedure still has its own risks and limitations. For example, BRTO requires injection of a sclerosing agent (e.g. sodium tetradecyl sulfate or ethanolamine oleate), which has been associated with pulmonary venothrombotic embolization, portal vein thrombosis, anaphylactic reaction, hemolysis, renal tubular disturbance and acute renal failure. Furthermore, BRTO involves an indwelling occlusive balloon that remains inflated for hours, thus resulting in lengthy procedure times with increased necessary hospital resources and serious potential complication for balloon rupture. Despite these risks for BRTO complications, the procedure has been largely adopted by the IR community for its high success in controlling acute GVB, improving liver function, and well-documented improvement of hepatic encephalopathy.
In 2013, Gwon et al. modified BRTO with a vascular plug replacing the indwelling balloon to minimize the technical and clinical complications associated with BRTO with results suggesting plug-assisted RTO (PARTO) to be simple, safe, and an effective treatment for GV. A year later, Lee et al., presented their own preliminary findings with a modified BRTO procedure involving coils instead of balloons with the conclusion that coil-assisted retrograde transvenous obliteration (CARTO) treatment of portal hypertension variceal bleeding was a feasible and safer alternative than BRTO. A case report by Terada et al. highlighted the benefits to CARTO in a few ways: 1) if the shunt was not conducive to balloon placement then CARTO was a superior alternative 2) a steerable catheter reduced the required access routes and 3) steerable catheters allow for selective catheterization of acute-angle branching vessels. During the past decade, CARTO and PARTO have evolved as a simpler and possibly safer alternative to BRTO with comparable efficacy and favorable complication profiles. Yet, despite the promising preliminary results during these last decades on RTO for GVB, there is limited data in regard to its long-term efficacy. Furthermore, given the everchanging treatments for prophylactic treatment of GVB per AASLD guidelines, there is not enough data to support RTO as a preemptive intervention to protect against primary GVB. This study is aimed at exploring this latter question.
Per AASLD guidelines, primary prophylactic management for prevention of first GVB is a non-selective beta blocker. These same guidelines recommend against either TIPS or BRTO for primary prophylaxis of GVB. Yet the AASLD guidelines for treatment change considerably after patient endorses their first variceal bleeding. For instance, if the patient had a GOV1 hemorrhage, first-line treatment against gastric variceal rebleeding is both a non-selective beta blocker and an endoscopic variceal ligation. If the patient had a GOV2 or IGV1 hemorrhage, then first-line treatment against gastric variceal rebleeding can be either TIPS or BRTO. While these guidelines provide a framework for gastric variceal management, currently, non-selective beta-blockers serve as the only prophylactic treatment against primary GVB. The current study challenges this guideline to see whether CARTO or PARTO, a procedure with high efficacy and high safety profile, can be integrated as an alternative prophylactic treatment against primary GVB.
In the investigators' recent retrospective study (unpublished data), the investigators demonstrated that the cumulative survival rates in patients who received prophylactic CARTO/PARTO were 94% and 62% at 60 and 120 months. In contrast, those who received CARTO/PARTO for active bleeding were 43% and 0% at 60 and 120 months, respectively. There was a significant difference between the two groups (p=0.00035). This finding needs to be further investigated in prospective trials to validate these findings, which could potentially change how patients with GV are treated.
In this study, the investigators will perform a single-center, prospective, randomized controlled trial to evaluate the effectiveness in reducing primary GVB between preemptive RTO and the current conservative standard of care in patients with gastric varices. The results of this study will guide clinical practice and standard of care management of RTO as a possible alternative to prophylactic treatment against primary GVB. The study will also collect extensive follow-up care in all participants to continue cultivating data for RTO-associated complications and assessing its effect on necessary secondary interventions. As RTO procedures continue to evolve and become more widely used, this study will have the ability to contribute important information towards the indication and guidance of CARTO as an alternative prophylactic treatment.
- Conditions
- Gastric Varices
- Being tested
- Non-selective beta blockers, Retrograde transvenous obliteration
- Keywords
- varices, stomach, gastric, hepatic encephalopathy, gastric variceal bleeding, bleeding, retrograde transvenous obliteration
- Medical subject headings
- Esophageal and Gastric Varices, Varicose Veins, Hepatic Encephalopathy, Hemorrhage
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Non-selective beta blockersDrug
Non-selective beta blockers are used in patients who have not had a previous variceal bleed to prevent bleeding by reducing blood pressure in the liver. These drugs also work by blocking beta receptors that reduce cardiac output and by causing vessel constriction in the abdominal organs, which lowers blood flow to the liver and the existing varices.
Retrograde transvenous obliterationProcedure or surgery
Also called CARTO, PARTO, BRTO, RTO, RTOs
Pre-emptive retrograde transvenous obliteration will be performed in patients randomized to this arm to evaluate the effectiveness in decreasing gastric variceal bleeding. Either CARTO or PARTO (coil or plug-assisted retrograde transvenous obliteration) will be performed using EMBOLIZATION COILS or VASCULAR PLUGS of different sizes based on the size of the shunt. Additionally, Gelfoam (collagen sponges) slurry will be injected into the shunt and varices to completely obliterate them.
| Study group | Role | What they receive |
|---|---|---|
| Non-selective beta blockers | Active comparator | Non-selective beta blockers prescribed according to standard of care treatment guidelines. These may include propranolol, nadolol, and timolol. Receives: Drug: Non-selective beta blockers |
| Retrograde transvenous obliteration (RTO) | Active comparator | Pre-emptive treatment with retrograde transvenous obliteration Receives: Procedure: Retrograde transvenous obliteration |
What is being measured
The primary outcome is the main question the study is designed to answer.
Episodes of variceal bleeding
To monitor and assess the effectiveness of decreasing gastric variceal bleeding episodes between those receiving pre-emptive retrograde transvenous obliteration versus conservative management with non-selective beta blockers.
Measured: 2 years
Secondary outcomes (2)
Complications
To compare complications related to retrograde transvenous obliteration versus conservative management with non-selective beta blockers, including worsening of gastric varices, other bleeding, ascites, or hepatic encephalopathy
Measured: 2 years
Transplant-free survival
To compare the short term (1 month), mid-term (3 months and 6 months), and long-term (every 3 months up to two years) outcomes of episodes of gastric variceal bleeding, overall survival and transplant-free survival, complications, and secondary interventions.
Measured: Two years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Sep 2025
- Study startOct 2026 (estimated)
- Primary completionNov 2027 (estimated)
- Study completionNov 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (9)Papers the sponsor has linked to this study.
- Other trials for Gastric VaricesStudies of the same condition, open and under way.
- More trials run by University of California, Los AngelesThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 68 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of California, Los Angeles
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Edward Wolfgang Lee, MD, University of California, Los Angeles
- Investigators
- Edward W. Lee, MD, PhD, Principal investigator, University of California, Los Angeles
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07168395
- Sponsor's protocol ID
- 25-1721
- Acronym
- PRADA
- Status last verified
- Jul 2026
- First submitted
- 1 Sep 2025
- Last updated
- 2 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Terada K, Ogi T, Yoneda N, Yokka A, Sugiura T, Koda W, Kobayashi S, Gabata T. Coil-assisted retrograde transvenous obliteration (CARTO) for the treatment of gastric varices via a single access route using steerable microcatheter: a case report. CVIR Endovasc. 2020 Jun 14;3(1):30. doi: 10.1186/s42155-020-00124-3.
PubMed 32537683Gwon DI, Ko GY, Yoon HK, Sung KB, Kim JH, Shin JH, Ko HK, Song HY. Gastric varices and hepatic encephalopathy: treatment with vascular plug and gelatin sponge-assisted retrograde transvenous obliteration--a primary report. Radiology. 2013 Jul;268(1):281-7. doi: 10.1148/radiol.13122102. Epub 2013 Mar 12.
PubMed 23481167Lee EW, Saab S, Gomes AS, Busuttil R, McWilliams J, Durazo F, Han SH, Goldstein L, Tafti BA, Moriarty J, Loh CT, Kee ST. Coil-Assisted Retrograde Transvenous Obliteration (CARTO) for the Treatment of Portal Hypertensive Variceal Bleeding: Preliminary Results. Clin Transl Gastroenterol. 2014 Oct 2;5(10):e61. doi: 10.1038/ctg.2014.12.
PubMed 25273155Miyoshi H, Ohshiba S, Matsumoto A, Takada K, Umegaki E, Hirata I. Haptoglobin prevents renal dysfunction associated with intravariceal infusion of ethanolamine oleate. Am J Gastroenterol. 1991 Nov;86(11):1638-41.
PubMed 1951242Hashizume M, Kitano S, Yamaga H, Sugimachi K. Haptoglobin to protect against renal damage from ethanolamine oleate sclerosant. Lancet. 1988 Aug 6;2(8606):340-1. doi: 10.1016/s0140-6736(88)92400-2. No abstract available.
PubMed 2899760Cho SK, Shin SW, Lee IH, Do YS, Choo SW, Park KB, Yoo BC. Balloon-occluded retrograde transvenous obliteration of gastric varices: outcomes and complications in 49 patients. AJR Am J Roentgenol. 2007 Dec;189(6):W365-72. doi: 10.2214/AJR.07.2266.
PubMed 18029851Kanagawa H, Mima S, Kouyama H, Gotoh K, Uchida T, Okuda K. Treatment of gastric fundal varices by balloon-occluded retrograde transvenous obliteration. J Gastroenterol Hepatol. 1996 Jan;11(1):51-8. doi: 10.1111/j.1440-1746.1996.tb00010.x.
PubMed 8672742Sarin SK, Lahoti D, Saxena SP, Murthy NS, Makwana UK. Prevalence, classification and natural history of gastric varices: a long-term follow-up study in 568 portal hypertension patients. Hepatology. 1992 Dec;16(6):1343-9. doi: 10.1002/hep.1840160607.
PubMed 1446890Wani ZA, Bhat RA, Bhadoria AS, Maiwall R, Choudhury A. Gastric varices: Classification, endoscopic and ultrasonographic management. J Res Med Sci. 2015 Dec;20(12):1200-7. doi: 10.4103/1735-1995.172990.
PubMed 26958057
Study at a glance
From the registry record, last updated by the sponsor on 2 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pre-emptive RTO for An Early Detected Gastric Varices in CT/MR Angiogram Trial (PRADA Trial)
- ClinicalTrials.gov ID
- NCT07168395
- Acronym / sponsor ID
- PRADA / 25-1721
- Conditions
- Gastric Varices
- Keywords
- varices, stomach, gastric, hepatic encephalopathy, gastric variceal bleeding, bleeding, retrograde transvenous obliteration
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 68 participants (estimated)
- Lead sponsor
- University of California, Los AngelesUniversity, hospital or other
- Study start
- Oct 2026 (estimated)
- Primary completion
- Nov 2027 (estimated)
- Study completion
- Nov 2028 (estimated)
- First posted
- 11 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A number of treatment modalities are currently in use for gastric variceal bleeding (GVB). Balloon-occluded, plug-assisted, and coil-assisted retrograde transvenous obliteration (RTO) procedures are described in the literature as treatments for GVB after a bleeding episode occurs. Preliminary data suggests that prophylactic treatment of gastric varices may improve patient outcomes compared to conservative management. This study aims to compare pre-emptive treatment of gastric varices with current recommended medical management in a randomized prospective study design. Eligible patients will be randomized to receive RTO or to continue conservative management. Patients will be followed for up to 2 years for comparison of clinical outcomes, including episodes of gastric variceal bleeding, overall survival and transplant-free survival, complications, and secondary interventions.
Detailed description
Gastroesophageal varices occur in approximately 50% of patients with liver cirrhosis. Specifically, gastric varices (GV) are responsible for roughly 10-30% of all variceal hemorrhage which is less than their counterpart esophageal varices. Despite their lower recurrence rates, gastric variceal bleeds (GVB) are associated with higher mortality, with an estimated 35-90% of patients developing rebleeding after achieving hemostasis.
Currently, there are several treatments for GVB that include endoscopic injection therapies, percutaneous antegrade transhepatic obliteration (ATO), transjugular portosystemic shunt placement (TIPS), splenic artery embolization (SAE), and surgical treatment. However, these procedures in previously studied trials have well-documented risks that compromise clinical outcomes. One specific interventional radiology procedure that has maintained a positive reputation in its use for gastric variceal bleeds is balloon-occluded retrograde transvenous obliteration (BRTO). This was first reported by Kanagawa et al. in the early 1990s; BRTO remains a well-accepted method of treatment of gastric fundal varices with gastrorenal or gastrophrenic shunts because of its minimally invasive nature and highly effective results, with studies showing up to 95% clinical success rate in stopping variceal bleeding. However, this procedure still has its own risks and limitations. For example, BRTO requires injection of a sclerosing agent (e.g. sodium tetradecyl sulfate or ethanolamine oleate), which has been associated with pulmonary venothrombotic embolization, portal vein thrombosis, anaphylactic reaction, hemolysis, renal tubular disturbance and acute renal failure. Furthermore, BRTO involves an indwelling occlusive balloon that remains inflated for hours, thus resulting in lengthy procedure times with increased necessary hospital resources and serious potential complication for balloon rupture. Despite these risks for BRTO complications, the procedure has been largely adopted by the IR community for its high success in controlling acute GVB, improving liver function, and well-documented improvement of hepatic encephalopathy.
In 2013, Gwon et al. modified BRTO with a vascular plug replacing the indwelling balloon to minimize the technical and clinical complications associated with BRTO with results suggesting plug-assisted RTO (PARTO) to be simple, safe, and an effective treatment for GV. A year later, Lee et al., presented their own preliminary findings with a modified BRTO procedure involving coils instead of balloons with the conclusion that coil-assisted retrograde transvenous obliteration (CARTO) treatment of portal hypertension variceal bleeding was a feasible and safer alternative than BRTO. A case report by Terada et al. highlighted the benefits to CARTO in a few ways: 1) if the shunt was not conducive to balloon placement then CARTO was a superior alternative 2) a steerable catheter reduced the required access routes and 3) steerable catheters allow for selective catheterization of acute-angle branching vessels. During the past decade, CARTO and PARTO have evolved as a simpler and possibly safer alternative to BRTO with comparable efficacy and favorable complication profiles. Yet, despite the promising preliminary results during these last decades on RTO for GVB, there is limited data in regard to its long-term efficacy. Furthermore, given the everchanging treatments for prophylactic treatment of GVB per AASLD guidelines, there is not enough data to support RTO as a preemptive intervention to protect against primary GVB. This study is aimed at exploring this latter question.
Per AASLD guidelines, primary prophylactic management for prevention of first GVB is a non-selective beta blocker. These same guidelines recommend against either TIPS or BRTO for primary prophylaxis of GVB. Yet the AASLD guidelines for treatment change considerably after patient endorses their first variceal bleeding. For instance, if the patient had a GOV1 hemorrhage, first-line treatment against gastric variceal rebleeding is both a non-selective beta blocker and an endoscopic variceal ligation. If the patient had a GOV2 or IGV1 hemorrhage, then first-line treatment against gastric variceal rebleeding can be either TIPS or BRTO. While these guidelines provide a framework for gastric variceal management, currently, non-selective beta-blockers serve as the only prophylactic treatment against primary GVB. The current study challenges this guideline to see whether CARTO or PARTO, a procedure with high efficacy and high safety profile, can be integrated as an alternative prophylactic treatment against primary GVB.
In the investigators' recent retrospective study (unpublished data), the investigators demonstrated that the cumulative survival rates in patients who received prophylactic CARTO/PARTO were 94% and 62% at 60 and 120 months. In contrast, those who received CARTO/PARTO for active bleeding were 43% and 0% at 60 and 120 months, respectively. There was a significant difference between the two groups (p=0.00035). This finding needs to be further investigated in prospective trials to validate these findings, which could potentially change how patients with GV are treated.
In this study, the investigators will perform a single-center, prospective, randomized controlled trial to evaluate the effectiveness in reducing primary GVB between preemptive RTO and the current conservative standard of care in patients with gastric varices. The results of this study will guide clinical practice and standard of care management of RTO as a possible alternative to prophylactic treatment against primary GVB. The study will also collect extensive follow-up care in all participants to continue cultivating data for RTO-associated complications and assessing its effect on necessary secondary interventions. As RTO procedures continue to evolve and become more widely used, this study will have the ability to contribute important information towards the indication and guidance of CARTO as an alternative prophylactic treatment.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Non-selective beta blockers | Active comparator | Drug: Non-selective beta blockersNon-selective beta blockers prescribed according to standard of care treatment guidelines. These may include propranolol, nadolol, and timolol. |
| Retrograde transvenous obliteration (RTO) | Active comparator | Procedure: Retrograde transvenous obliterationPre-emptive treatment with retrograde transvenous obliteration |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (11 listed)
- Age > 18 years
- Patients with compensated cirrhosis with a higher risk of decompensation based on AASLD 2023 Practice Guidance (Kaplan et al) - no ascites with endoscopic visualization of varices
- Confirmed diagnosis of gastric varices either through CT, MRI, or Endoscopy.
- No imaging (LIRAD4 or 5) or tumor marker (AFP) evidence of HCC or other malignancy
- MELD < 20
Key exclusion criteria (10 listed)
- Age <18 years
- Patients with decompensated cirrhosis based on AASLD 2023 Practice Guidance (Kaplan et al)
- Cardiac failure
- Active variceal bleeding
- History of gastroesophageal variceal bleeding
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Non-selective beta blockersNon-selective beta blockers are used in patients who have not had a previous variceal bleed to prevent bleeding by reducing blood pressure in the liver. These drugs also work by blocking beta receptors that reduce cardiac output and by causing vessel constriction in the abdominal organs, which lowers blood flow to the liver and the existing varices. | Drug | Non-selective beta blockers |
| Retrograde transvenous obliterationAlso: CARTO, PARTO, BRTO, RTO, RTOsPre-emptive retrograde transvenous obliteration will be performed in patients randomized to this arm to evaluate the effectiveness in decreasing gastric variceal bleeding. Either CARTO or PARTO (coil or plug-assisted retrograde transvenous obliteration) will be performed using EMBOLIZATION COILS or VASCULAR PLUGS of different sizes based on the size of the shunt. Additionally, Gelfoam (collagen sponges) slurry will be injected into the shunt and varices to completely obliterate them. | Procedure or surgery | Retrograde transvenous obliteration (RTO) |
Primary outcome
Episodes of variceal bleeding
Time frame: 2 years
To monitor and assess the effectiveness of decreasing gastric variceal bleeding episodes between those receiving pre-emptive retrograde transvenous obliteration versus conservative management with non-selective beta blockers.
2 secondary outcomes
Complications
Time frame: 2 years
Transplant-free survival
Time frame: Two years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Jul 2026.
- Background: PubMed 32537683Terada K, Ogi T, Yoneda N, Yokka A, Sugiura T, Koda W, Kobayashi S, Gabata T. Coil-assisted retrograde transvenous obliteration (CARTO) for the treatment of gastric varices via a single access route using steerable microcatheter: a case report. CVIR Endovasc. 2020 Jun 14;3(1):30. doi: 10.1186/s42155-020-00124-3.
- Background: PubMed 23481167Gwon DI, Ko GY, Yoon HK, Sung KB, Kim JH, Shin JH, Ko HK, Song HY. Gastric varices and hepatic encephalopathy: treatment with vascular plug and gelatin sponge-assisted retrograde transvenous obliteration--a primary report. Radiology. 2013 Jul;268(1):281-7. doi: 10.1148/radiol.13122102. Epub 2013 Mar 12.
- Background: PubMed 25273155Lee EW, Saab S, Gomes AS, Busuttil R, McWilliams J, Durazo F, Han SH, Goldstein L, Tafti BA, Moriarty J, Loh CT, Kee ST. Coil-Assisted Retrograde Transvenous Obliteration (CARTO) for the Treatment of Portal Hypertensive Variceal Bleeding: Preliminary Results. Clin Transl Gastroenterol. 2014 Oct 2;5(10):e61. doi: 10.1038/ctg.2014.12.
- Background: PubMed 1951242Miyoshi H, Ohshiba S, Matsumoto A, Takada K, Umegaki E, Hirata I. Haptoglobin prevents renal dysfunction associated with intravariceal infusion of ethanolamine oleate. Am J Gastroenterol. 1991 Nov;86(11):1638-41.
- Background: PubMed 2899760Hashizume M, Kitano S, Yamaga H, Sugimachi K. Haptoglobin to protect against renal damage from ethanolamine oleate sclerosant. Lancet. 1988 Aug 6;2(8606):340-1. doi: 10.1016/s0140-6736(88)92400-2. No abstract available.
- Background: PubMed 18029851Cho SK, Shin SW, Lee IH, Do YS, Choo SW, Park KB, Yoo BC. Balloon-occluded retrograde transvenous obliteration of gastric varices: outcomes and complications in 49 patients. AJR Am J Roentgenol. 2007 Dec;189(6):W365-72. doi: 10.2214/AJR.07.2266.
- Background: PubMed 8672742Kanagawa H, Mima S, Kouyama H, Gotoh K, Uchida T, Okuda K. Treatment of gastric fundal varices by balloon-occluded retrograde transvenous obliteration. J Gastroenterol Hepatol. 1996 Jan;11(1):51-8. doi: 10.1111/j.1440-1746.1996.tb00010.x.
- Background: PubMed 1446890Sarin SK, Lahoti D, Saxena SP, Murthy NS, Makwana UK. Prevalence, classification and natural history of gastric varices: a long-term follow-up study in 568 portal hypertension patients. Hepatology. 1992 Dec;16(6):1343-9. doi: 10.1002/hep.1840160607.
- Background: PubMed 26958057Wani ZA, Bhat RA, Bhadoria AS, Maiwall R, Choudhury A. Gastric varices: Classification, endoscopic and ultrasonographic management. J Res Med Sci. 2015 Dec;20(12):1200-7. doi: 10.4103/1735-1995.172990.
- Individual participant dataSharing planned: No
Related trials for Gastric Varices
RecruitingObservational study
The Value of Spleen Thickness and Spleen Diameter for Gastroesophageal Varices Diagnosis in Compensated Cirrhosis
Liver Cirrhosis, Gastroesophageal Varices
Enrolling by invitationObservational study
Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Detachable Coils
Arteriovenous Malformation, Gastrointestinal Bleed
Recruiting
EUS-Guided Coil and Glue vs Glue Injection for Bleeding Gastric Varices in Cirrhosis
Gastric Varices Bleeding, Cirrhosis
Not yet recruitingObservational study
Baveno VIII Criteria for Portal Hypertension in Egyptian Patients
Compensated Liver Disease, Esophageal Varices
Recruiting
A Prospective, Multicenter, Randomized Controlled Trial Investigating the Impact of Fasting Duration on Postoperative Rebleeding Following Esophageal Variceal Ligation.
Esophageal Varices
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Edward W. Lee, MD, PhD principal investigator
University of California, Los Angeles
Questions about this trial
What is this clinical trial studying?
A study testing Non-selective beta blockers and Retrograde transvenous obliteration in people with Gastric Varices, run by University of California, Los Angeles.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 11 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 2 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Edward W. Lee, MD, PhD (310-267-8771, edwardlee@mednet.ucla.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Episodes of variceal bleeding (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07168395, which also lists 9 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jul 2026.