Hepatocellular CarcinomaNCT07395635
Phase II Trial of Immunonutrition in Hepatectomy
A study testing Immunonutrition in people with Hepatocellular Carcinoma and ASA I-III Patients, run by Tata Memorial Centre at 1 site in India.
Trial summary
A randomised open labelled study to evalaute the impact of immunonutrition in Patients Undergoing Hepatectomies for Liver Tumors Read more about this study
- Who is it for?
- Ages 18 to 90 years
- Conditions the study is for
- Hepatocellular Carcinoma, ASA I-III Patients
- What is being tested?
- Immunonutrition
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteIndia
- Study dates
- 3 Oct 2025to 31 Jan 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 to 90 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients with liver tumors planned for major hepatectomies (defined as resection of >/= 3 liver segments)
- Age above 18 years
- ASA class I-III
Who cannot join
- Preoperative severe renal failure (estimated glomerular filtration rate < 30 ml/min)
- History of hypersensitivity to arginine, omega-3 fatty acids, or nucleotide 3. Inability to take oral nutrition
- 4. Pregnancy 5. Mental condition rendering the subject unable to understand the nature, endpoints and consequences of the trial
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
India1 site, 1 recruiting
- Recruiting
Dr. Shraddha Patkar
Mumbai, Maharashtra, 400012
Dr. Shraddha Patkar, MD MCh, 9820074818, drshraddhapatkar@gmail.com
Dr. Shraddha Patkar, MD MCh
About this study
Official title: Impact of Immunonutrition in Patients Undergoing Hepatectomies for Liver Tumors: A Randomized Controlled Phase II Trial
A randomised open labelled study to evalaute the impact of immunonutrition in Patients Undergoing Hepatectomies for Liver Tumors
Read the detailed description
Major hepatectomy remains a cornerstone in the curative management of primary and secondary liver tumors. Despite substantial advances in surgical techniques, anesthesia, and perioperative care, hepatectomy continues to be associated with considerable postoperative morbidity and mortality. Reported morbidity rates range from 22% to 40%, while mortality rates vary between 4% and 11%, largely driven by postoperative infectious complications, liver failure, and systemic inflammatory responses. Optimization of preoperative patient status, particularly nutritional and immune function, has therefore emerged as a critical area of interest to improve postoperative outcomes.
Immunonutrition, defined as nutritional supplementation enriched with specific substrates such as arginine, omega-3 fatty acids, and nucleotides, has demonstrated beneficial effects in patients undergoing major gastrointestinal surgery, pancreatic resections, and liver transplantation. These formulations are thought to modulate immune response, attenuate postoperative inflammation, improve protein synthesis, and enhance wound healing. However, evidence supporting the routine use of immunonutrition in patients undergoing hepatectomy remains limited and inconsistent. Existing meta-analyses suggest reductions in postoperative infectious complications and length of hospital stay, but uncertainty persists regarding its overall clinical benefit, particularly in relation to objective nutritional and immunological markers.
The prognostic nutritional index (PNI), calculated using serum albumin levels and total lymphocyte count, is a validated composite marker reflecting both nutritional and immune status. Multiple studies and meta-analyses have shown that a higher preoperative PNI is associated with improved postoperative outcomes and survival following hepatectomy. Furthermore, recent evidence indicates that inflammatory and nutritional biomarkers, including dynamic changes in albumin-based indices, are strong predictors of postoperative morbidity. These findings suggest that targeted immunonutritional interventions capable of improving PNI may translate into meaningful clinical benefits.
Against this background, the present study is designed to evaluate whether preoperative immunonutrition can improve PNI in patients undergoing major hepatectomy for liver tumors. The central hypothesis is that short-term preoperative immunonutrition leads to a measurable improvement in PNI compared with standard nutritional care.
The aim of the study is to assess the effect of preoperative immunonutrition on the prognostic nutritional index in patients planned for major hepatectomy.
The primary objective is to compare the mean change in PNI between patients receiving immunonutrition and those receiving standard nutritional care.
Secondary objectives include evaluating the impact of immunonutrition on postoperative complications, incidence of post-hepatectomy liver failure, length of intensive care unit stay, overall hospital stay, and 90-day postoperative mortality.
This is an open-label, randomized, phase II controlled trial conducted at Tata Memorial Hospital, Mumbai. Adult patients (≥18 years) with liver tumors scheduled for major hepatectomy, defined as resection of three or more liver segments, and classified as ASA physical status I-III will be eligible for inclusion. Patients with severe renal dysfunction, hypersensitivity to immunonutritional components, inability to tolerate oral intake, pregnancy, or conditions impairing informed consent will be excluded.
Eligible patients providing written informed consent will be randomized in a 1:1 ratio into one of two study groups using a centrally generated permuted-block randomization sequence. The intervention group will receive preoperative immunonutrition in addition to their usual oral intake for seven consecutive days prior to surgery. The immunonutritional supplement will be administered in weight-adjusted doses and compliance will be monitored through patient records and telephonic reminders. The control group will continue with their usual oral intake; patients identified as malnourished in this group will receive standard nutritional supplementation as per institutional protocols.
Blood samples will be collected at baseline and repeated on the day prior to surgery to assess serum albumin, lymphocyte count, and inflammatory markers. PNI will be calculated at baseline and preoperatively to evaluate the effect of the intervention. Postoperative assessments will include serial liver function tests, documentation of complications up to 90 days, and recording of ICU and hospital stay durations.
A total of 100 patients (50 per group) will be enrolled over two years, providing adequate power to detect a clinically meaningful difference in PNI between groups. Data will be collected prospectively and analyzed using appropriate statistical methods. Continuous variables will be summarized using means and standard deviations, while categorical variables will be expressed as proportions. The primary endpoint will be analyzed by comparing mean PNI differences between groups, with secondary outcomes evaluated using standard comparative statistical tests.
In summary, this study seeks to generate high-quality prospective evidence on the role of preoperative immunonutrition in improving nutritional and immune status, as measured by PNI, in patients undergoing major hepatectomy. The findings have the potential to inform perioperative nutritional strategies and improve postoperative outcomes in this high-risk surgical population.
- Conditions
- Hepatocellular Carcinoma, ASA I-III Patients
- Being tested
- Immunonutrition
- Keywords
- Immunonutrition, Hepatectomy
- Medical subject headings
- Carcinoma, Hepatocellular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ImmunonutritionDietary supplement
Also called PENTASURE IMMUNOMAX POWDER
In addition to their usual intake, patients in the intervention arm will be prescribed for each of the 7 consecutive days preceding surgery 6-9 scoops PENTASURE Immunomax® powder (120-180g per day)
| Study group | Role | What they receive |
|---|---|---|
| Intervention Arm | Experimental | Immunomax® Powder- Participant in this group will receive Immunomac Powder 7 consecutive days preceding surgery in a dose of 6-9 scoops (120-180g per day), based on their bodyweight. Receives: Dietary Supplement: Immunonutrition |
| Standard Arm | No intervention | Participant in this group will be advised to continue with their usual oral intake. Patients in this group assessed as having malnutrition will be provided with a standard nutritional supplement (Fortisip®, Nutricia) twice daily (providing 600 kcal energy, 24 g protein), in addition to their usual intake, for the period preceding and including 7 days prior to surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
Preoperative immunonutrition improves prognostic nutritional index (PNI)
improvement in prognostic nutritional index after maor hepatectomies calculated with the help of Prognostic Nutritional Index (PNI) = [(10 × serum albumin (g/dL)) + (0.005 × total lymphocyte count)].
Measured: 90 days
Secondary outcomes (5)
Incidence of postoperative complications
number of complications in both arm major with Clavien-Dindo (CD) classification for adverse events 2. Incidence of post-hepatectomies liver failure (PHLF) 3. Length of ICU stay 4. Length of hospital stay, 5. Incidence of 90 days mortality
Measured: upto 3 months
Incidence of post-hepatectomies liver failure (PHLF)
nuber of patients undergoing hepatice failure in both study arm after the major hepatectomies define by ndicated by elevated total bilirubin (\(>22\ \mu \text{mol/L}\)) and increased INR (\(>1.2\)) on or after the fifth postoperative day (POD 5), as per ISGLS criteria
Measured: Perioperative upto day 5
Length of ICU stay
number of days participant spent in ICU after hepatectomy till discharge in both treatment group
Measured: Perioperative upto day 30
Length of hospital stay,
number of days participant spent in hospital after hepatectomy till discharge in both treatment group
Measured: Perioperative upto day 30
Incidence of 90 days mortality
death of participant from any cause after the hepatecomy in both treatment groups
Measured: Perioperative upto day 90
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Feb 2026
- Study start3 Oct 2025
- Primary completion31 Oct 2027 (estimated)
- Study completion31 Jan 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (10)Papers the sponsor has linked to this study.
- Other trials for Hepatocellular CarcinomaStudies of the same condition, open and under way.
- More trials run by Tata Memorial CentreThe 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
- Open labelled, Phase II randomized controlled trial Interventional Study
- Masking
- None (open label)
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Tata Memorial Centre
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Dr Shraddha Patkar, Tata Memorial Centre
- Investigators
- Dr. Shraddha Patkar, MD MCh, Principal investigator, Professor and surgeon
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07395635
- Sponsor's protocol ID
- Study no: 4783
- Status last verified
- Feb 2026
- First submitted
- 29 Jan 2026
- Last updated
- 9 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Zhang H, Li D, Li J. Prognostic significance of preoperative prognostic nutritional index in hepatocellular carcinoma after curative hepatectomy: a meta-analysis and systemic review. Front Nutr. 2024 Dec 23;11:1433528. doi: 10.3389/fnut.2024.1433528. eCollection 2024.
PubMed 39764415Solanki SL, Kaur J, Gupta AM, Patkar S, Joshi R, Ambulkar RP, Patil A, Goel M. Cancer related nutritional and inflammatory markers as predictive parameters of immediate postoperative complications and long-term survival after hepatectomies. Surg Oncol. 2021 Jun;37:101526. doi: 10.1016/j.suronc.2021.101526. Epub 2021 Feb 4.
PubMed 33582497Zhang C, Chen B, Jiao A, Li F, Wang B, Sun N, Zhang J. The benefit of immunonutrition in patients undergoing hepatectomy: a systematic review and meta-analysis. Oncotarget. 2017 Aug 8;8(49):86843-86852. doi: 10.18632/oncotarget.20045. eCollection 2017 Oct 17.
PubMed 29156839Wong CS, Praseedom R, Liau SS. Perioperative immunonutrition in hepatectomy: A systematic review and meta-analysis. Ann Hepatobiliary Pancreat Surg. 2020 Nov 30;24(4):396-414. doi: 10.14701/ahbps.2020.24.4.396.
PubMed 33234742Gao B, Luo J, Liu Y, Zhong F, Yang X, Gan Y, Su S, Li B. Clinical Efficacy of Perioperative Immunonutrition Containing Omega-3-Fatty Acids in Patients Undergoing Hepatectomy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Ann Nutr Metab. 2020;76(6):375-386. doi: 10.1159/000509979. Epub 2020 Dec 11.
PubMed 33311018Beevi Ss S, Pottakkat B. Effect of Immunonutrition on the Liver Function Status of End-Stage Liver Disease Patients Waiting/Referred for Liver Transplant: A Randomized Controlled Trial. Cureus. 2023 Mar 30;15(3):e36923. doi: 10.7759/cureus.36923. eCollection 2023 Mar.
PubMed 37128515Zhang G, Zhao B, Deng T, He X, Chen Y, Zhong C, Chen J. Impact of perioperative immunonutrition on postoperative outcomes in pancreaticoduodenectomy: a systematic review and meta-analysis of randomized controlled trials. BMC Gastroenterol. 2024 Nov 16;24(1):412. doi: 10.1186/s12876-024-03510-6.
PubMed 39550568Markar S, Mariette C, Bonnetain F, Lundell L, Rosati R, de Manzoni G, Bonavina L, Tucker O, Plum P, D'Journo XB, Van Daele D, Cogill G, Santi S, Farran L, Iranzo V, Pera M, Veziant J, Piessen G. Immunonutrition to improve the quality of life of upper gastrointestinal cancer patients undergoing neoadjuvant treatment prior to surgery (NEOIMMUNE): double-blind randomized controlled multicenter clinical trial. Dis Esophagus. 2025 Jan 7;38(1):doae113. doi: 10.1093/dote/doae113.
PubMed 39863958Franken LC, Schreuder AM, Roos E, van Dieren S, Busch OR, Besselink MG, van Gulik TM. Morbidity and mortality after major liver resection in patients with perihilar cholangiocarcinoma: A systematic review and meta-analysis. Surgery. 2019 May;165(5):918-928. doi: 10.1016/j.surg.2019.01.010. Epub 2019 Mar 11.
PubMed 30871811van Keulen AM, Buttner S, Erdmann JI, Hagendoorn J, Hoogwater FJH, IJzermans JNM, Neumann UP, Polak WG, De Jonge J, Olthof PB, Koerkamp BG. Major complications and mortality after resection of intrahepatic cholangiocarcinoma: A systematic review and meta-analysis. Surgery. 2023 Apr;173(4):973-982. doi: 10.1016/j.surg.2022.11.027. Epub 2022 Dec 27.
PubMed 36577599
Study at a glance
From the registry record, last updated by the sponsor on 9 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Immunonutrition in Patients Undergoing Hepatectomies for Liver Tumors: A Randomized Controlled Phase II Trial
- ClinicalTrials.gov ID
- NCT07395635
- Acronym / sponsor ID
- Study no: 4783
- Conditions
- Hepatocellular Carcinoma, ASA I-III Patients
- Keywords
- Immunonutrition, Hepatectomy
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Tata Memorial CentreUniversity, hospital or other
- Study start
- 3 Oct 2025 (actual)
- Primary completion
- 31 Oct 2027 (estimated)
- Study completion
- 31 Jan 2028 (estimated)
- First posted
- 9 Feb 2026 (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 randomised open labelled study to evalaute the impact of immunonutrition in Patients Undergoing Hepatectomies for Liver Tumors
Detailed description
Major hepatectomy remains a cornerstone in the curative management of primary and secondary liver tumors. Despite substantial advances in surgical techniques, anesthesia, and perioperative care, hepatectomy continues to be associated with considerable postoperative morbidity and mortality. Reported morbidity rates range from 22% to 40%, while mortality rates vary between 4% and 11%, largely driven by postoperative infectious complications, liver failure, and systemic inflammatory responses. Optimization of preoperative patient status, particularly nutritional and immune function, has therefore emerged as a critical area of interest to improve postoperative outcomes.
Immunonutrition, defined as nutritional supplementation enriched with specific substrates such as arginine, omega-3 fatty acids, and nucleotides, has demonstrated beneficial effects in patients undergoing major gastrointestinal surgery, pancreatic resections, and liver transplantation. These formulations are thought to modulate immune response, attenuate postoperative inflammation, improve protein synthesis, and enhance wound healing. However, evidence supporting the routine use of immunonutrition in patients undergoing hepatectomy remains limited and inconsistent. Existing meta-analyses suggest reductions in postoperative infectious complications and length of hospital stay, but uncertainty persists regarding its overall clinical benefit, particularly in relation to objective nutritional and immunological markers.
The prognostic nutritional index (PNI), calculated using serum albumin levels and total lymphocyte count, is a validated composite marker reflecting both nutritional and immune status. Multiple studies and meta-analyses have shown that a higher preoperative PNI is associated with improved postoperative outcomes and survival following hepatectomy. Furthermore, recent evidence indicates that inflammatory and nutritional biomarkers, including dynamic changes in albumin-based indices, are strong predictors of postoperative morbidity. These findings suggest that targeted immunonutritional interventions capable of improving PNI may translate into meaningful clinical benefits.
Against this background, the present study is designed to evaluate whether preoperative immunonutrition can improve PNI in patients undergoing major hepatectomy for liver tumors. The central hypothesis is that short-term preoperative immunonutrition leads to a measurable improvement in PNI compared with standard nutritional care.
The aim of the study is to assess the effect of preoperative immunonutrition on the prognostic nutritional index in patients planned for major hepatectomy.
The primary objective is to compare the mean change in PNI between patients receiving immunonutrition and those receiving standard nutritional care.
Secondary objectives include evaluating the impact of immunonutrition on postoperative complications, incidence of post-hepatectomy liver failure, length of intensive care unit stay, overall hospital stay, and 90-day postoperative mortality.
This is an open-label, randomized, phase II controlled trial conducted at Tata Memorial Hospital, Mumbai. Adult patients (≥18 years) with liver tumors scheduled for major hepatectomy, defined as resection of three or more liver segments, and classified as ASA physical status I-III will be eligible for inclusion. Patients with severe renal dysfunction, hypersensitivity to immunonutritional components, inability to tolerate oral intake, pregnancy, or conditions impairing informed consent will be excluded.
Eligible patients providing written informed consent will be randomized in a 1:1 ratio into one of two study groups using a centrally generated permuted-block randomization sequence. The intervention group will receive preoperative immunonutrition in addition to their usual oral intake for seven consecutive days prior to surgery. The immunonutritional supplement will be administered in weight-adjusted doses and compliance will be monitored through patient records and telephonic reminders. The control group will continue with their usual oral intake; patients identified as malnourished in this group will receive standard nutritional supplementation as per institutional protocols.
Blood samples will be collected at baseline and repeated on the day prior to surgery to assess serum albumin, lymphocyte count, and inflammatory markers. PNI will be calculated at baseline and preoperatively to evaluate the effect of the intervention. Postoperative assessments will include serial liver function tests, documentation of complications up to 90 days, and recording of ICU and hospital stay durations.
A total of 100 patients (50 per group) will be enrolled over two years, providing adequate power to detect a clinically meaningful difference in PNI between groups. Data will be collected prospectively and analyzed using appropriate statistical methods. Continuous variables will be summarized using means and standard deviations, while categorical variables will be expressed as proportions. The primary endpoint will be analyzed by comparing mean PNI differences between groups, with secondary outcomes evaluated using standard comparative statistical tests.
In summary, this study seeks to generate high-quality prospective evidence on the role of preoperative immunonutrition in improving nutritional and immune status, as measured by PNI, in patients undergoing major hepatectomy. The findings have the potential to inform perioperative nutritional strategies and improve postoperative outcomes in this high-risk surgical population.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Open labelled, Phase II randomized controlled trial Interventional Study
| Arm | Type | Receives |
|---|---|---|
| Intervention Arm | Experimental | Dietary Supplement: ImmunonutritionImmunomax® Powder- Participant in this group will receive Immunomac Powder 7 consecutive days preceding surgery in a dose of 6-9 scoops (120-180g per day), based on their bodyweight. |
| Standard Arm | No intervention | –Participant in this group will be advised to continue with their usual oral intake. Patients in this group assessed as having malnutrition will be provided with a standard nutritional supplement (Fortisip®, Nutricia) twice daily (providing 600 kcal energy, 24 g protein), in addition to their usual intake, for the period preceding and including 7 days prior to surgery |
Who may qualify
- Ages
- 18 to 90 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Patients with liver tumors planned for major hepatectomies (defined as resection of >/= 3 liver segments)
- Age above 18 years
- ASA class I-III
Key exclusion criteria (3 listed)
- Preoperative severe renal failure (estimated glomerular filtration rate < 30 ml/min)
- History of hypersensitivity to arginine, omega-3 fatty acids, or nucleotide 3. Inability to take oral nutrition
- 4. Pregnancy 5. Mental condition rendering the subject unable to understand the nature, endpoints and consequences of the trial
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 |
|---|---|---|
| ImmunonutritionAlso: PENTASURE IMMUNOMAX POWDERIn addition to their usual intake, patients in the intervention arm will be prescribed for each of the 7 consecutive days preceding surgery 6-9 scoops PENTASURE Immunomax® powder (120-180g per day) | Dietary supplement | Intervention Arm |
Primary outcome
Preoperative immunonutrition improves prognostic nutritional index (PNI)
Time frame: 90 days
improvement in prognostic nutritional index after maor hepatectomies calculated with the help of Prognostic Nutritional Index (PNI) = [(10 × serum albumin (g/dL)) + (0.005 × total lymphocyte count)].
5 secondary outcomes
Incidence of postoperative complications
Time frame: upto 3 months
Incidence of post-hepatectomies liver failure (PHLF)
Time frame: Perioperative upto day 5
Length of ICU stay
Time frame: Perioperative upto day 30
Length of hospital stay,
Time frame: Perioperative upto day 30
Incidence of 90 days mortality
Time frame: Perioperative upto day 90
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 9 Feb 2026.
- Results publication: PubMed 39764415Zhang H, Li D, Li J. Prognostic significance of preoperative prognostic nutritional index in hepatocellular carcinoma after curative hepatectomy: a meta-analysis and systemic review. Front Nutr. 2024 Dec 23;11:1433528. doi: 10.3389/fnut.2024.1433528. eCollection 2024.
- Results publication: PubMed 33582497Solanki SL, Kaur J, Gupta AM, Patkar S, Joshi R, Ambulkar RP, Patil A, Goel M. Cancer related nutritional and inflammatory markers as predictive parameters of immediate postoperative complications and long-term survival after hepatectomies. Surg Oncol. 2021 Jun;37:101526. doi: 10.1016/j.suronc.2021.101526. Epub 2021 Feb 4.
- Results publication: PubMed 29156839Zhang C, Chen B, Jiao A, Li F, Wang B, Sun N, Zhang J. The benefit of immunonutrition in patients undergoing hepatectomy: a systematic review and meta-analysis. Oncotarget. 2017 Aug 8;8(49):86843-86852. doi: 10.18632/oncotarget.20045. eCollection 2017 Oct 17.
- Results publication: PubMed 33234742Wong CS, Praseedom R, Liau SS. Perioperative immunonutrition in hepatectomy: A systematic review and meta-analysis. Ann Hepatobiliary Pancreat Surg. 2020 Nov 30;24(4):396-414. doi: 10.14701/ahbps.2020.24.4.396.
- Results publication: PubMed 33311018Gao B, Luo J, Liu Y, Zhong F, Yang X, Gan Y, Su S, Li B. Clinical Efficacy of Perioperative Immunonutrition Containing Omega-3-Fatty Acids in Patients Undergoing Hepatectomy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Ann Nutr Metab. 2020;76(6):375-386. doi: 10.1159/000509979. Epub 2020 Dec 11.
- Results publication: PubMed 37128515Beevi Ss S, Pottakkat B. Effect of Immunonutrition on the Liver Function Status of End-Stage Liver Disease Patients Waiting/Referred for Liver Transplant: A Randomized Controlled Trial. Cureus. 2023 Mar 30;15(3):e36923. doi: 10.7759/cureus.36923. eCollection 2023 Mar.
- Results publication: PubMed 39550568Zhang G, Zhao B, Deng T, He X, Chen Y, Zhong C, Chen J. Impact of perioperative immunonutrition on postoperative outcomes in pancreaticoduodenectomy: a systematic review and meta-analysis of randomized controlled trials. BMC Gastroenterol. 2024 Nov 16;24(1):412. doi: 10.1186/s12876-024-03510-6.
- Results publication: PubMed 39863958Markar S, Mariette C, Bonnetain F, Lundell L, Rosati R, de Manzoni G, Bonavina L, Tucker O, Plum P, D'Journo XB, Van Daele D, Cogill G, Santi S, Farran L, Iranzo V, Pera M, Veziant J, Piessen G. Immunonutrition to improve the quality of life of upper gastrointestinal cancer patients undergoing neoadjuvant treatment prior to surgery (NEOIMMUNE): double-blind randomized controlled multicenter clinical trial. Dis Esophagus. 2025 Jan 7;38(1):doae113. doi: 10.1093/dote/doae113.
- Results publication: PubMed 30871811Franken LC, Schreuder AM, Roos E, van Dieren S, Busch OR, Besselink MG, van Gulik TM. Morbidity and mortality after major liver resection in patients with perihilar cholangiocarcinoma: A systematic review and meta-analysis. Surgery. 2019 May;165(5):918-928. doi: 10.1016/j.surg.2019.01.010. Epub 2019 Mar 11.
- Results publication: PubMed 36577599van Keulen AM, Buttner S, Erdmann JI, Hagendoorn J, Hoogwater FJH, IJzermans JNM, Neumann UP, Polak WG, De Jonge J, Olthof PB, Koerkamp BG. Major complications and mortality after resection of intrahepatic cholangiocarcinoma: A systematic review and meta-analysis. Surgery. 2023 Apr;173(4):973-982. doi: 10.1016/j.surg.2022.11.027. Epub 2022 Dec 27.
- 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.
Dr. Shraddha Patkar, MD MCh principal investigator
Professor and surgeon
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Immunonutrition in people with Hepatocellular Carcinoma and ASA I-III Patients, run by Tata Memorial Centre at 1 site in India.
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 3 inclusion and 3 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: looking for participants now, as of the sponsor's last update on 9 Feb 2026. 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 India. 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?
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 Dr. Shraddha Patkar, MD MCh (9820074818, drshraddhapatkar@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Preoperative immunonutrition improves prognostic nutritional index (PNI) (time frame: 90 days). 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 NCT07395635, which also lists 10 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 9 Feb 2026.