MedDataX Logo

Impact of a Transmission Checklist in Post Anesthesia Care Unit on Immediate Respiratory Complications

NCT ID: NCT03972423

Last Updated: 2020-11-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

560 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-02-18

Study Completion Date

2020-07-07

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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).

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Anesthesia Postoperative Complications Anesthesia Complication

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

checklist postoperative complication anesthesia information transmission care unit

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

IRCTC group

\- The IRCTC group, consisting of all patients included in the 3rd phase of the study and for whom the transmission of information in PACU is carried out using the IRCTC.

With or wiyhout a checklist

Intervention Type OTHER

The evaluation of the impact of the use of this Checklist will be done in comparison with the standard transmission practice

CONTROL group

\- The CONTROL group, consisting of all patients included in the 1st phase of the study and for whom the transmission of information in PACU is carried out according to the usual practice.

With or wiyhout a checklist

Intervention Type OTHER

The evaluation of the impact of the use of this Checklist will be done in comparison with the standard transmission practice

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

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

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Dr. Frédéric MARTIN

UNKNOWN

Sponsor Role collaborator

Ramsay Générale de Santé

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Frederic Martin

Role: PRINCIPAL_INVESTIGATOR

Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Les Franciscaines Clinic

Versailles, IDF, France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

References

Explore related publications, articles, or registry entries linked to this study.

Jaulin F, Lopes T, Martin F. Standardised handover process with checklist improves quality and safety of care in the postanaesthesia care unit: the Postanaesthesia Team Handover trial. Br J Anaesth. 2021 Dec;127(6):962-970. doi: 10.1016/j.bja.2021.07.002. Epub 2021 Aug 5.

Reference Type DERIVED
PMID: 34364652 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ID-RCB : 2018-A01825-50

Identifier Type: -

Identifier Source: org_study_id