NCT02824783

Brief Summary

The aim of the study is to investigate the quality of life and satisfaction of patient who underwent colorectal surgery using an enhanced recovery protocol when back home. In this retrospective study patients will be telephoned and asked to answer a questionnaire.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
41

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2016

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2016

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 25, 2016

Completed
6 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2016

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 7, 2016

Completed
Last Updated

January 3, 2018

Status Verified

December 1, 2017

Enrollment Period

6 months

First QC Date

June 25, 2016

Last Update Submit

December 29, 2017

Conditions

Surgery

Keywords

colorectal surgeryenhanced recovery

Outcome Measures

Primary Outcomes (1)

  • Quality of life (0 to ten numeric scale + questionnaire)

    0 to ten numeric scale + questionnaire

    first month after leaving the hospital

Secondary Outcomes (3)

  • Satisfaction (0 to ten numeric scale + questionnaire)

    first month after leaving the hospital

  • Pain (0 to ten numeric scale + questionnaire)

    first month after leaving the hospital

  • Fatigue (0 to ten numeric scale + questionnaire)

    first month after leaving the hospital

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

all patients included in our GRACE database since the 1st of October 2015

You may qualify if:

  • all patients included in our GRACE database

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital of Liege

Liège, 4000, Belgium

Location

Study Officials

  • Jean Joris, M.D.

    Department of Anesthesiology, CHU Liege, Belgium

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor and Chief Department of Anesthesiology

Study Record Dates

First Submitted

June 25, 2016

First Posted

July 7, 2016

Study Start

January 1, 2016

Primary Completion

July 1, 2016

Study Completion

July 1, 2016

Last Updated

January 3, 2018

Record last verified: 2017-12

Data Sharing

IPD Sharing
Will not share

Locations

BE(1)