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Study to see the outcome of intravenous phosphatesupplementation in live liver donors

Not Applicable
Registration Number
CTRI/2019/01/016914
Lead Sponsor
Institute of Liver Biliary Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All donors evaluated as per institutional protocol for donor hepatectomy and found fit

Those who consent.

Exclusion Criteria

Patients refusing to consent for inclusion in the study.

Minor hepatectomy

Those who develop profound hypophosphatemia in the control group

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study the outcome of phosphate supplementation in reducing the occurrence of postoperative complicationsTimepoint: till discharge
Secondary Outcome Measures
NameTimeMethod
Duration of hospital stayTimepoint: Till discharge;Duration of ICU stayTimepoint: Till discharge;To analyze the role of phosphate supplementation in liver regenerationTimepoint: Till discharge;To study the correlation between phosphate levels and trend in post-operative LFTsTimepoint: Till discharge;To study the serum phosphate levels and its trend post operativelyTimepoint: Till discharge
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