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Nutritional supplementation and prehab for Biliary Tract Cancer
N/A
Waitlist Available
Led By Prosanto Chaudhury, MD
Research Sponsored by McGill University Health Centre/Research Institute of the McGill University Health Centre
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Subjects eligible to enter the prehabilitation program will include those aged 18 and above and referred electively for resection of malignancies.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 and 1 week pre-operatively, 4 and 8 weeks post-operatively
Awards & highlights
No Placebo-Only Group
Summary
1. To determine whether a combined nutritional support program and exercise-based prehabilitation is superior to nutritional support alone in increasing functional recovery and reducing post-operative morbidity after surgery for HPB malignancy. 2. To understand which measures of immediate surgical recovery are sensitive to prehabilitation interventions and predict change in later outcome measures.
Eligible Conditions
- Biliary Tract Cancer
- Colorectal Cancer
- Liver Cancer
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 8 and 1 week pre-operatively, 4 and 8 weeks post-operatively
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 and 1 week pre-operatively, 4 and 8 weeks post-operatively
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in six minute walk test
Secondary study objectives
Depression and anxiety
Fatigue
Health-related quality of life (HRQL)
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Nutritional supplementation and prehabExperimental Treatment1 Intervention
The first group (pre-hab) will receive both nutritional supplementation and a prehabilitation program.
Group II: Prehab exerciseActive Control1 Intervention
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Who is running the clinical trial?
McGill University Health Centre/Research Institute of the McGill University Health CentreLead Sponsor
470 Previous Clinical Trials
166,897 Total Patients Enrolled
Prosanto Chaudhury, MDPrincipal InvestigatorMcGill University Health Centre/Research Institute of the McGill University Health Centre
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