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RecruitingNCT06475911

Impact of Peri-Operative Hyponatremia on Postoperative Outcomes in Major HPB Surgeries for Cancers

Status
Recruiting
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Institute of Liver and Biliary Sciences, India · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The present study is being designed to study the impact and predictive nature of perioperative hyponatremia on post operative outcomes in patients undergoing Major HPB surgeries for cancers. Major hepatobiliary-pancreatic surgeries will be defined as follows- * Pancreaticoduodenectomy, * Hemihepatectomy or greater with or without caudate lobectomy * Extrahepatic bile duct resection * Extended cholecystectomy * Distal Pancreatectomy with or without splenectomy The primary Objective of the study would be to compare post operative major morbidities and early mortality (\<90 day) in major HPB surgeries done for cancer patients with and without peri-operative hyponatremia. (\<135mmoL/L). Development of systemic complications and long term outcomes (overall survival and disease free survival) will also be evaluated. It will be an observational study consisting of both, a retrospective arm and a prospective arm. All consecutive patients undergoing major HPB surgery from 2010 till 30th June 2024 will be included in the study.

Detailed description

Primary objective: To compare post operative major morbidities and early mortality (\<90 day) in major HPB surgeries done for cancer in patients with and without peri-operative hyponatremia. (\<135mmoL/L) Secondary objectives: To compare the following in patients undergoing major HPB surgeries for cancer in patients with and without peri-operative hyponatremia (\<135mmoL/L) * Post operative Systemic complications and * Long term outcomes * OS- POD1 till death/ last follow up (30th Sep 2024). * DFS- Surgical resection till first detected recurrence of cancer or last follow up (30th Sep 2024) without recurrence. * Study design- Observational study- Retrospective and prospective. * Study period- Data collection will be done from time of ethical clearance till 30th June 2024. * Intervention - None * Monitoring and assessment- Clinical profile of the patient and symptoms will be serially followed during the patients post operative OPD visits. * STATISTICAL ANALYSIS: 1. Continuous variables- with Student t test and Mann Whitney U test as appropriate. 2. Categorical data - Chi square or Fischer exact test. Besides the above, appropriate analysis will be done at the time of final data analysis. 3. Significance will be seen at 5 % level (p\<0.05). 4. Adequate subgroup analysis and multivariate regression analysis will be done. * Adverse effects - No adverse effect is expected to occur out of the study protocol. * Stopping rule - Not Valid

Conditions

Timeline

Start date
2023-10-23
Primary completion
2024-12-30
Completion
2024-12-30
First posted
2024-06-26
Last updated
2024-06-26

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT06475911. Inclusion in this directory is not an endorsement.