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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01732159
Recruitment Status : Completed
First Posted : November 22, 2012
Last Update Posted : April 21, 2015
Sponsor:
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris

Study Description
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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.

Condition or disease Intervention/treatment Phase
Ambulatory Surgery Programmed Other: Checklist Not Applicable

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.
Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 4093 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Official Title: Impact of a Checklist on the Rate of Late Cancellation in Ambulatory Surgery
Study Start Date : November 2012
Actual Primary Completion Date : January 2014
Actual Study Completion Date : April 2014
Arms and Interventions
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Arm Intervention/treatment
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


Outcome Measures
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Primary Outcome Measures :
  1. Decrease in the rate of late cancellation [ Time Frame: At day 0 (the day of the surgery) ]

Secondary Outcome Measures :
  1. Improvement of the organization of the ambulatory unit [ Time Frame: At day 0 (the day of the surgery) ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
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
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01732159


Locations
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France
Cochin Hospital
Paris, France, 75014
Sponsors and Collaborators
Assistance Publique - Hôpitaux de Paris
Investigators
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Principal Investigator: Jean-Pierre BETHOUX, MD, PhD Cochin Hospital
More Information
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Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier: NCT01732159    
Other Study ID Numbers: K110601
First Posted: November 22, 2012    Key Record Dates
Last Update Posted: April 21, 2015
Last Verified: April 2015
Keywords provided by Assistance Publique - Hôpitaux de Paris:
Ambulatory surgery
Checklist
Cancellation