Acute AbdomenNCT05419440
Laparoscopic Drainage Versus Interventional Radiology In Management Of Appendicular Abscess :
A study testing laparoscopic drainage of appendicular abscess in people with Acute Abdomen, run by Zagazig University at 1 site in Egypt.
Trial summary
This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. Read more about this study
- Who is it for?
- Ages 16 years and older
- Conditions the study is for
- Acute Abdomen
- What is being tested?
- laparoscopic drainage of appendicular abscess
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 172 participants
- Where
- 1 siteEgypt
- Study dates
- 10 Jan 2020to 2 Feb 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 16 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Patients ≥16- ≤60 years-old with appendicular abscess
- with early sepsis.
- no septic shock.
- ASA I \& II.
- no other pathology .
- candidate for laparoscopy .
Who cannot join
- <16- >60 years-old .
- septic shock.
- appendicular mass.
- , ASA III .
- previous abdominal operations.
- immune compromised patients .
Show all 9Show fewer
- patients with immune suppressive therapy.
- pregnant patients not
- candidate for laparoscopy
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Laparoscopic Drainage Versus Interventional Radiology In Management Of Appendicular Abscess : A Randomized Controlled Trial.
This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. The study was prospectively approved by Zagazig University Faculty of Medicine Institutional Review Board (Approval Number: 55342/24.1.2020). The sample size was 172 patients divided into two equal group group (1) laparoscopic group involved 86 patients \& group (2) interventional radiology group involved 86 patients.
Read the detailed description
This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. The study was prospectively approved by Zagazig University Faculty of Medicine Institutional Review Board (Approval Number: 55342/24.1.2020), and was retrospectively submitted in clinicaltrials.gov in September 2021 (NCT05051683). The study was performed in accordance with the code of ethics of the World Medical Association (Declaration of Helsinki) for studies involving human subjects. Written informed consent was obtained from all participants after explaining to them all the study procedures with its benefits and hazards. Patients ≥16- ≤60 years-old, with appendicular abscess , with early sepsis , no septic shock , ASA I \& II , no other pathology and candidate for laparoscopy were deemed eligible for randomization. We excluded patients who were <16- >60 years-old, septic shock, appendicular mass, ASA III , previous abdominal operations, immune compromised patients , patients with immune suppressive therapy, pregnant patients and not candidate for laparoscopy.
Involved patients were simply randomized at a 1:1 ratio to "laparoscopic Group (LG)" or "Interventional Radiology Group (IG)" via the drawing of sealed envelopes containing computer-generated random numbers prepared by a third party before the start of the procedure.
The sample size was calculated by using open Epi program depending on the following data ; confidence interval 95%, power of the test 80%, ratio of unexposed/exposed 1, percent of patients with complications after management of appendicular abscess by interventional radiology 15 %, and those managed by laparoscopy 2 % , odds ratio 8.7 , and risk ratio 7.5, So the calculated sample size equal 172 patients divided into two equal group.
Primary and secondary outcomes were fecal fistula , recurrent collection and quality of life in each group after the procedures during the 3-months follow-up period, respectively.
Diagnosis After full history taking ( throbbing pain at right iliac fossa several days ago ) and complete physical examination ( fluctuant high grade fever especially at evening , severe pain \& tenderness at right iliac fossa , toxic manifestations), appendicular abscess was clinically suspected and then confirmed by laboratory investigations (complete blood picture (WBC count more than 16000), liver and kidney functions, coagulation profile), radiological imaging (abdominal US or CT abdomen with oral and I.V contrast confirms appendicular abscess) , in laparoscopic group we exclude patients with other pathology after laparoscopic exploration However, the radiology finding was consistent with appendicular abscess.
Intervention For laparoscopic group ( included 86 patients ) , the patients were subjected to the following steps after the diagnosis has been confirmed as appendicular abscess. The patients were taken rapidly to operative theater , general anesthesia was given , patients were put in supine position , sterilization of the abdomen from subcostal margin to pubic bone was done , ports insertion was done , one 10 mm port supra-umbilical , one 5mm port at left iliac fossa , one 5mm port at right iliac fossa , insertion of the 10 mm port was done first by open method or versus needle , insufflation of co2 up to 14 mm.hg was done after 10 mm port insertion , exploration of the abdomen first by 10 mm telescope , to exclude other pathology and confirm the diagnosis ( we exclude patients with other pathology after laparoscopic exploration ) , then insertion of other two ports under vision , removal of any adhesions first , irrigation \& suction whole the abdomen first with warm saline 0.9% , access to caecum by tilting the table head down and to left to pull all intestine away from caecum , access to caecum and remove any adhesions with surrounding by sharp \& blunt dissection , then access to appendicular abscess by sharp and blunt dissection , drain all the pus by suction , irrigation with warm saline , after complete separation of the appendix from surrounding \& complete drainage of pus \& removal of all necrotic tissue , removal of the remnant appendix , in cases with healthy base of appendix ,we closed the stump with endo-loop , in case with unhealthy base , we closed the stump by suturing by ethibond 2/0 in two layers in case with little edema \& inflammation of caecum ( sutures not cut through ) , in cases with marked edema and inflammation of caecum , we close the site of base by omental patch fixed by taking full thickness sutures in wall of caecum and pass through omental patch , we examine any leak by pressing on caecum and observe any fecal matter comes \& air leak test , in all cases we made irrigation \& suction with 2000cc warm saline and put large drain at pelvis to be removed later according to its discharge , deflation of the abdomen and close the port sites. Then patients were kept in hospital under observation till drain removal.
For interventional radiology group ( included 86 patients ) , patients were subjected for drain insertion or pig catheter insertion at right iliac fossa under a complete sterilized filed by radiologist , then daily wash from drain or pig catheter by gentamycin \& metronidazole till drain discharge comes clear fluid , then drain removed according the amount of discharge and doing us confirm there is no residual.
Statistical analysis Analysis of data was performed using SPSS (Statistical Package of Social Services) version 22. Quantitative variables were described as mean (±SD, standard deviation) and median (range) according to Shapiro test of normality. Qualitative variables were described as a number and a percent. Chi-square test was used to compare qualitative variables between the 2 groups. Fisher exact test was used when one expected cell or more are less than 5. Unpaired t-test was used to compare quantitative variables, in parametric data (SD < 30% of the mean). Mann Whitney test was used instead of unpaired t-test in non-parametric data (SD > 30% of the mean). The results were considered statistically significant when the significant probability was less than 0.05 (P < 0.05). P-value < 0.001 was considered highly statistically significant (HS), and P-value ≥ 0.05 was considered statistically insignificant (NS).
- Conditions
- Acute Abdomen
- Being tested
- laparoscopic drainage of appendicular abscess
- Keywords
- appendicular abscess , laparoscopy
- Medical subject headings
- Abdomen, Acute
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
laparoscopic drainage of appendicular abscessProcedure or surgery
access to caecum and remove any adhesions with surrounding by sharp \& blunt dissection , then access to appendicular abscess by sharp and blunt dissection after complete separation of the appendix from surrounding \& complete drainage of pus \& removal of all necrotic tissue , removal of the remnant appendix , in cases with healthy base of appendix ,we closed the stump with endo-loop , in case with unhealthy base , we closed the stump by suturing by ethibond 2/0 in two layers in case with little edema \& inflammation of caecum ( sutures not cut through ) , in cases with marked edema and inflammation of caecum , we close the site of base by omental patch fixed by taking full thickness sutures in wall of caecum and pass through omental patch , we examine any leak by pressing on caecum and observe any fecal matter comes \& air leak test , in all cases we put large drain at pelvis
| Study group | Role | What they receive |
|---|---|---|
| laparoscopic drainage of appendicular abscess | Active comparator | laparoscopic drainage of appendicular abscess laparoscopy drainage of pus ,excision of appendix and putting a drain Receives: Procedure: laparoscopic drainage of appendicular abscess |
| interventional radiology for management of appendicular abscess | No intervention | insertion of a drain or pig tail under sonar or ct guided |
What is being measured
The primary outcome is the main question the study is designed to answer.
incidence of complications after laparoscopic drainage of appendicular abscess
incidence of complications after laparoscopic drainage of appendicular abscess
Measured: within one week after laparoscopic drainage of the appendicular abscess
Secondary outcomes (1)
incidence of mortality after laparoscopic drainage of appendicular abscess
incidence of mortality after laparoscopic drainage of appendicular abscess
Measured: within one month after laparoscopic drainage of appendicular abscess
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Jun 2022
- Study start10 Jan 2020
- Primary completion2 Feb 2022
- Study completion2 Feb 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Acute AbdomenStudies of the same condition, open and under way.
- More trials run by Zagazig UniversityThe 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
- Model description
- This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. The study was prospectively approved by Zagazig University Faculty of Medicine Institutional Review Board (Approval Number: 55342/24.1.2020), The sample size was 172 patients divided into two equal group group (1) laparoscopic group involved 86 patients \& group (2) interventional radiology group involved 86 patients.
- Masking
- None (open label)
- Enrolment
- 172 participants (actual)
Sponsor and investigators
- Lead sponsor
- Zagazig University
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Said Mohamed Said Abdou Negm, Zagazig University
- Investigators
- Said Mohamed Negm, MD, Principal investigator, Zagazig University Hospitals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05419440
- Sponsor's protocol ID
- General Surgery Departement
- Status last verified
- Jun 2022
- First submitted
- 9 Jun 2022
- Last updated
- 15 Jun 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 15 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Laparoscopic Drainage Versus Interventional Radiology In Management Of Appendicular Abscess : A Randomized Controlled Trial.
- ClinicalTrials.gov ID
- NCT05419440
- Acronym / sponsor ID
- General Surgery Departement
- Conditions
- Acute Abdomen
- Keywords
- appendicular abscess , laparoscopy
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 172 participants (actual)
- Lead sponsor
- Zagazig UniversityOther government
- Study start
- 10 Jan 2020 (actual)
- Primary completion
- 2 Feb 2022 (actual)
- Study completion
- 2 Feb 2022 (actual)
- First posted
- 15 Jun 2022 (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.
This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. The study was prospectively approved by Zagazig University Faculty of Medicine Institutional Review Board (Approval Number: 55342/24.1.2020). The sample size was 172 patients divided into two equal group group (1) laparoscopic group involved 86 patients \& group (2) interventional radiology group involved 86 patients.
Detailed description
This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. The study was prospectively approved by Zagazig University Faculty of Medicine Institutional Review Board (Approval Number: 55342/24.1.2020), and was retrospectively submitted in clinicaltrials.gov in September 2021 (NCT05051683). The study was performed in accordance with the code of ethics of the World Medical Association (Declaration of Helsinki) for studies involving human subjects. Written informed consent was obtained from all participants after explaining to them all the study procedures with its benefits and hazards. Patients ≥16- ≤60 years-old, with appendicular abscess , with early sepsis , no septic shock , ASA I \& II , no other pathology and candidate for laparoscopy were deemed eligible for randomization. We excluded patients who were <16- >60 years-old, septic shock, appendicular mass, ASA III , previous abdominal operations, immune compromised patients , patients with immune suppressive therapy, pregnant patients and not candidate for laparoscopy.
Involved patients were simply randomized at a 1:1 ratio to "laparoscopic Group (LG)" or "Interventional Radiology Group (IG)" via the drawing of sealed envelopes containing computer-generated random numbers prepared by a third party before the start of the procedure.
The sample size was calculated by using open Epi program depending on the following data ; confidence interval 95%, power of the test 80%, ratio of unexposed/exposed 1, percent of patients with complications after management of appendicular abscess by interventional radiology 15 %, and those managed by laparoscopy 2 % , odds ratio 8.7 , and risk ratio 7.5, So the calculated sample size equal 172 patients divided into two equal group.
Primary and secondary outcomes were fecal fistula , recurrent collection and quality of life in each group after the procedures during the 3-months follow-up period, respectively.
Diagnosis After full history taking ( throbbing pain at right iliac fossa several days ago ) and complete physical examination ( fluctuant high grade fever especially at evening , severe pain \& tenderness at right iliac fossa , toxic manifestations), appendicular abscess was clinically suspected and then confirmed by laboratory investigations (complete blood picture (WBC count more than 16000), liver and kidney functions, coagulation profile), radiological imaging (abdominal US or CT abdomen with oral and I.V contrast confirms appendicular abscess) , in laparoscopic group we exclude patients with other pathology after laparoscopic exploration However, the radiology finding was consistent with appendicular abscess.
Intervention For laparoscopic group ( included 86 patients ) , the patients were subjected to the following steps after the diagnosis has been confirmed as appendicular abscess. The patients were taken rapidly to operative theater , general anesthesia was given , patients were put in supine position , sterilization of the abdomen from subcostal margin to pubic bone was done , ports insertion was done , one 10 mm port supra-umbilical , one 5mm port at left iliac fossa , one 5mm port at right iliac fossa , insertion of the 10 mm port was done first by open method or versus needle , insufflation of co2 up to 14 mm.hg was done after 10 mm port insertion , exploration of the abdomen first by 10 mm telescope , to exclude other pathology and confirm the diagnosis ( we exclude patients with other pathology after laparoscopic exploration ) , then insertion of other two ports under vision , removal of any adhesions first , irrigation \& suction whole the abdomen first with warm saline 0.9% , access to caecum by tilting the table head down and to left to pull all intestine away from caecum , access to caecum and remove any adhesions with surrounding by sharp \& blunt dissection , then access to appendicular abscess by sharp and blunt dissection , drain all the pus by suction , irrigation with warm saline , after complete separation of the appendix from surrounding \& complete drainage of pus \& removal of all necrotic tissue , removal of the remnant appendix , in cases with healthy base of appendix ,we closed the stump with endo-loop , in case with unhealthy base , we closed the stump by suturing by ethibond 2/0 in two layers in case with little edema \& inflammation of caecum ( sutures not cut through ) , in cases with marked edema and inflammation of caecum , we close the site of base by omental patch fixed by taking full thickness sutures in wall of caecum and pass through omental patch , we examine any leak by pressing on caecum and observe any fecal matter comes \& air leak test , in all cases we made irrigation \& suction with 2000cc warm saline and put large drain at pelvis to be removed later according to its discharge , deflation of the abdomen and close the port sites. Then patients were kept in hospital under observation till drain removal.
For interventional radiology group ( included 86 patients ) , patients were subjected for drain insertion or pig catheter insertion at right iliac fossa under a complete sterilized filed by radiologist , then daily wash from drain or pig catheter by gentamycin \& metronidazole till drain discharge comes clear fluid , then drain removed according the amount of discharge and doing us confirm there is no residual.
Statistical analysis Analysis of data was performed using SPSS (Statistical Package of Social Services) version 22. Quantitative variables were described as mean (±SD, standard deviation) and median (range) according to Shapiro test of normality. Qualitative variables were described as a number and a percent. Chi-square test was used to compare qualitative variables between the 2 groups. Fisher exact test was used when one expected cell or more are less than 5. Unpaired t-test was used to compare quantitative variables, in parametric data (SD < 30% of the mean). Mann Whitney test was used instead of unpaired t-test in non-parametric data (SD > 30% of the mean). The results were considered statistically significant when the significant probability was less than 0.05 (P < 0.05). P-value < 0.001 was considered highly statistically significant (HS), and P-value ≥ 0.05 was considered statistically insignificant (NS).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This prospective randomized controlled clinical trial included all patients who developed the manifestations of appendicular abscess and referred to the Zagazig University Hospital Emergency Department between January 2020 and February 2022. The study was prospectively approved by Zagazig University Faculty of Medicine Institutional Review Board (Approval Number: 55342/24.1.2020), The sample size was 172 patients divided into two equal group group (1) laparoscopic group involved 86 patients \& group (2) interventional radiology group involved 86 patients.
| Arm | Type | Receives |
|---|---|---|
| laparoscopic drainage of appendicular abscess | Active comparator | Procedure: laparoscopic drainage of appendicular abscesslaparoscopic drainage of appendicular abscess laparoscopy drainage of pus ,excision of appendix and putting a drain |
| interventional radiology for management of appendicular abscess | No intervention | –insertion of a drain or pig tail under sonar or ct guided |
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (6 listed)
- Patients ≥16- ≤60 years-old with appendicular abscess
- with early sepsis.
- no septic shock.
- ASA I \& II.
- no other pathology .
Key exclusion criteria (9 listed)
- <16- >60 years-old .
- septic shock.
- appendicular mass.
- , ASA III .
- previous abdominal operations.
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 |
|---|---|---|
| laparoscopic drainage of appendicular abscessaccess to caecum and remove any adhesions with surrounding by sharp \& blunt dissection , then access to appendicular abscess by sharp and blunt dissection after complete separation of the appendix from surrounding \& complete drainage of pus \& removal of all necrotic tissue , removal of the remnant appendix , in cases with healthy base of appendix ,we closed the stump with endo-loop , in case with unhealthy base , we closed the stump by suturing by ethibond 2/0 in two layers in case with little edema \& inflammation of caecum ( sutures not cut through ) , in cases with marked edema and inflammation of caecum , we close the site of base by omental patch fixed by taking full thickness sutures in wall of caecum and pass through omental patch , we examine any leak by pressing on caecum and observe any fecal matter comes \& air leak test , in all cases we put large drain at pelvis | Procedure or surgery | laparoscopic drainage of appendicular abscess |
Primary outcome
incidence of complications after laparoscopic drainage of appendicular abscess
Time frame: within one week after laparoscopic drainage of the appendicular abscess
incidence of complications after laparoscopic drainage of appendicular abscess
1 secondary outcome
incidence of mortality after laparoscopic drainage of appendicular abscess
Time frame: within one month after laparoscopic drainage of appendicular abscess
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Jun 2022.
- Individual participant dataSharing planned: No
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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. This study is not recruiting at the moment.
Said Mohamed Negm, MD principal investigator
Zagazig University Hospitals
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing laparoscopic drainage of appendicular abscess in people with Acute Abdomen, run by Zagazig University at 1 site in Egypt.
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 6 inclusion and 9 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: finished, as of the sponsor's last update on 15 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
incidence of complications after laparoscopic drainage of appendicular abscess (time frame: within one week after laparoscopic drainage of the appendicular abscess). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 15 Jun 2022.