Dietary Survey After Colorectal Surgery Within an Enhanced Recovery Program (DIETERP).
DIETERP
Dietary Survey During the First Month After Colorectal Surgery Within an Enhanced Recovery Program
1 other identifier
observational
75
1 country
1
Brief Summary
This observational study will quantify caloric-protein intake in 75 patients undergoing colorectal surgery within an enhanced recovery program at CHU Liège. A dietary survey will be performed preoperatively and repeated postoperatively via telephone calls on Day + 3, Day + 7; Day + 15, and Day + 30, after leaving the hospital. The deficits observed will be correlated with the medical and surgical characteristics of the patients
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2018
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 15, 2018
CompletedFirst Submitted
Initial submission to the registry
November 20, 2018
CompletedFirst Posted
Study publicly available on registry
November 21, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 8, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
May 8, 2019
CompletedJuly 5, 2019
July 1, 2019
6 months
November 20, 2018
July 3, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
calorie and protein intakes
Using a dietary survey postoperative intake of calories and protein will be assessed in patients scheduled for colorectal surgery
one month after hospital discharge
Interventions
no intervention in this observational study
Eligibility Criteria
Any patient schedules for colorectal surgery with the ERP at CHU Liège (Belgium). Patients age must be greater than 18 years. There is no maximum limit of age.
You may qualify if:
- any patient scheduled for colorectal surgery within an ERP at CHU Liège
You may not qualify if:
- unable to answer the survey (cognitive disorders, bad knowledge of the French language)
- closure of loop ileostomy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital
Liège, Belgium
Study Officials
- PRINCIPAL INVESTIGATOR
Jean-François Brichant, MD
CHU Liege, Belgium
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of the Anesthesiology department
Study Record Dates
First Submitted
November 20, 2018
First Posted
November 21, 2018
Study Start
November 15, 2018
Primary Completion
May 8, 2019
Study Completion
May 8, 2019
Last Updated
July 5, 2019
Record last verified: 2019-07
Data Sharing
- IPD Sharing
- Will not share