Impact of a Checklist on the Rate of Late Cancellation in Ambulatory Surgery (AMBUPROG)

This study is currently recruiting participants.
Verified July 2013 by Assistance Publique - Hôpitaux de Paris
Sponsor:
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01732159
First received: November 19, 2012
Last updated: August 2, 2013
Last verified: July 2013
  Purpose

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.


Condition Intervention
Ambulatory Surgery Programmed
Other: Checklist

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Official Title: Impact of a Checklist on the Rate of Late Cancellation in Ambulatory Surgery

Further study details as provided by Assistance Publique - Hôpitaux de Paris:

Primary Outcome Measures:
  • Decrease in the rate of late cancellation [ Time Frame: At day 0 (the day of the surgery) ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Improvement of the organization of the ambulatory unit [ Time Frame: At day 0 (the day of the surgery) ] [ Designated as safety issue: No ]

Estimated Enrollment: 3580
Study Start Date: November 2012
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: June 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Administration of the checklist
Patients will be contacted by phone for administration of the checklist
Other: Checklist
he checklist will be administered to the patients by phone between 7 and 3 days before the surgery
No Intervention: No contact by phone
Patients who will not be contacted by phone

Detailed Description:

The checklist is administered to the patients by phone between 7 and 3 days before the surgery. Each item of the checklist is associated with a decisional algorithm that allows take care for patients in case of any problem.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • Patient programmed for endoscopy in ASU non surgical
  • Ambulatory surgery scheduled for orthogenic
  • Ambulatory surgery scheduled for urgency
  • Ambulatory surgery performed under local anesthesia
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01732159

Contacts
Contact: Jean-Pierre BETHOUX, MD +33142348301 jp.bethoux@htd.aphp.fr
Contact: Laurence Lecomte, MD, PhD +33 1 71 19 64 94 laurence.lecomte@nck.aphp.fr

Locations
France
Cochin Hospital Recruiting
Paris, France, 75014
Contact: Jean-Pierre BETHOUX, MD    +33142348301    jp.bethoux@htd.aphp.fr   
Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris
Investigators
Principal Investigator: Jean-Pierre BETHOUX, MD, PhD Cochin Hospital
  More Information

No publications provided

Responsible Party: Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier: NCT01732159     History of Changes
Other Study ID Numbers: K110601
Study First Received: November 19, 2012
Last Updated: August 2, 2013
Health Authority: France: Ministry of Health

Keywords provided by Assistance Publique - Hôpitaux de Paris:
Ambulatory surgery
Checklist
Cancellation

ClinicalTrials.gov processed this record on April 22, 2014