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Study identifier: NCT07560540 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Nutritional Intervention Implication in Enhanced Recovery After Surgery for Whipple Procedure

Condition: Pancreatic Cancer · Ampulla of Vater Adenocarcinoma · Billiary Track Cancer  ·  Sponsor: University of Veterinary and Animal Sciences, Lahore - Pakistan

PhaseNA
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objective of this research is to assess the impact of personalized nutritional intervention on postoperative complications and length of stay in Whipple's patients via assessing the parameters related to body composition, nutritional status, weight maintenance, biochemical profile (LFTs, RFTs, CBC, CRP, serum electrolytes, coagulation profile and HbA1c) and muscle preservation postoperatively. Moreover, enhanced recovery after surgery (ERAS) guidelines in Whipple's patients will also be monitored. Exactly 20 patients undergoing Whipple's Procedure/PPPD in 1 year will be recruited for the study. Medical nutrition therapy will include energy intake of 25- 30 Kcal/kg body weight and protein 1.2-1.5g/kg body weight. Enteral nutrition and parenteral nutrition will be given accordingly. After discharge, patients receiving chemotherapy and patients not receiving chemotherapy will be nutritionally intervened accordingly. Follow-ups will be done in the 2nd week, 3rd month and 6th month after surgery. Data will be analyzed using SPSS version 27. To assess the significant difference among study groups t-test, repeated measure analysis of variance (ANOVA) and regression model will be applied. The level of significance will be kept at 5%. t-test for treatment groups.

This description comes directly from the study's public registry record.

Talk to the study team

Javeriya Afzal, MPhil Food and Nutrition  ·  00923244090078  ·  javeriyaafzal23@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shalamar HospitalLahore, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT07560540