Impact of a Checklist on the Rate of Late Cancellation in Ambulatory Surgery
AMBUPROG
1 other identifier
interventional
4,093
1 country
1
Brief Summary
The purpose of this study is to evaluate the impact of a check list on the rate of late cancellation, i.e. the day before or the day of the ambulatory surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2012
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 1, 2012
CompletedFirst Submitted
Initial submission to the registry
November 19, 2012
CompletedFirst Posted
Study publicly available on registry
November 22, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2014
CompletedMarch 4, 2026
February 1, 2026
1.2 years
November 19, 2012
March 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Decrease in the rate of late cancellation
At day 0 (the day of the surgery)
Secondary Outcomes (1)
Improvement of the organization of the ambulatory unit
At day 0 (the day of the surgery)
Study Arms (2)
Administration of the checklist
EXPERIMENTALPatients will be contacted by phone for administration of the checklist
No contact by phone
NO INTERVENTIONPatients who will not be contacted by phone
Interventions
he checklist will be administered to the patients by phone between 7 and 3 days before the surgery
Eligibility Criteria
You may qualify if:
- Patient (adult or minor) for which ambulatory surgery is programmed in a multipurpose ASU
- Surgery under general anesthesia or loco
- Regional or neuroleptanalgesia3. Patient contacted by phone
- Patient does not oppose his participation in the study
You may not qualify if:
- Patient programmed for endoscopy in ASU non surgical
- Ambulatory surgery scheduled for orthogenic
- Ambulatory surgery scheduled for urgency
- Ambulatory surgery performed under local anesthesia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cochin Hospital
Paris, 75014, France
Related Publications (1)
Gaucher S, Boutron I, Marchand-Maillet F, Baron G, Douard R, Bethoux JP; AMBUPROG Group Investigators. Assessment of a Standardized Pre-Operative Telephone Checklist Designed to Avoid Late Cancellation of Ambulatory Surgery: The AMBUPROG Multicenter Randomized Controlled Trial. PLoS One. 2016 Feb 1;11(2):e0147194. doi: 10.1371/journal.pone.0147194. eCollection 2016.
PMID: 26829478RESULT
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jean-Pierre BETHOUX, MD, PhD
Cochin Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 19, 2012
First Posted
November 22, 2012
Study Start
November 1, 2012
Primary Completion
January 1, 2014
Study Completion
April 1, 2014
Last Updated
March 4, 2026
Record last verified: 2026-02