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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03972423
Other study ID # ID-RCB : 2018-A01825-50
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 18, 2019
Est. completion date July 7, 2020

Study information

Verified date May 2019
Source Ramsay Générale de Santé
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This work highlighted the beneficial role in terms of carers' satisfaction, quantity and quality of information transmitted.


Description:

Communication and information transmission problems are responsible for the majority of serious adverse events. The use of a checklist in the operating theatre has demonstrated its benefit in terms of reducing morbidity and mortality Regarding transmissions between caregivers, numerous studies have shown the great difference between the medical data of a patient in their file and the information transmitted. The authors recommend using checklists in order to standardise transmissions. This work highlighted the beneficial role in terms of carers' satisfaction, quantity and quality of information transmitted. On the other hand, no study has looked at the reduction of immediate postoperative complications in post anaesthesia care units (PACU).


Recruitment information / eligibility

Status Completed
Enrollment 560
Est. completion date July 7, 2020
Est. primary completion date February 18, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Male or Female over 18 admitted to PACU - Patient having understood the aims and the methods of the research - Patient having expressed their consent to the use of their data. - Subject registered with or beneficiary of a social security scheme Exclusion Criteria: - Patient participating in another clinical study - Acute or chronic respiratory insufficiency preoperatively - Protected patient: adult under guardianship, tutorship or other legal protection, deprived of liberty by judicial or administrative decision - Pregnant or lactating women

Study Design


Intervention

Other:
With or wiyhout a checklist
The evaluation of the impact of the use of this Checklist will be done in comparison with the standard transmission practice

Locations

Country Name City State
France Les Franciscaines Clinic Versailles IDF

Sponsors (2)

Lead Sponsor Collaborator
Ramsay Générale de Santé Dr. Frédéric MARTIN

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary arterial oxygen desaturation < 90% The primary endpoint is defined as the occurrence or not of arterial oxygen desaturation < 90% for more than 15 consecutive seconds in PACU. event of at least 15 second duration
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