Impact of a Pharmacist-anesthesiologist Collaboration During Anesthesia Consultation on Prevention of Perioperative Medication Errors of Patients in Programmed Surgery

NCT ID: NCT04013061

Last Updated: 2025-12-11

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

378 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-25

Study Completion Date

2021-09-30

Brief Summary

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The investigators will evaluate the efficiency of a pharmacist-anesthesiologist collaboration in the anesthetic consultation in the prevention of medical errors perioperatively in patients undergoing scheduled surgery

Detailed Description

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Conditions

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Surgical Procedures, Operative

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Standard consultation

Group Type NO_INTERVENTION

No interventions assigned to this group

Pharmacist-anesthesiologist consultation

Group Type EXPERIMENTAL

Pluridisciplinary consultation

Intervention Type OTHER

Pharmacist-anesthesiologist team will be present during the anesthetic consultation

Interventions

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Pluridisciplinary consultation

Pharmacist-anesthesiologist team will be present during the anesthetic consultation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The patient must have given their free and informed consent
* The patient must be a member or beneficiary of a health insurance plan
* The patient has at least one chronic medication prescription (associated with a chronic illness)
* The patient is hospitalized for a programmed surgery in the service of urology or digestive surgery at the CHU Nimes or orthopedic surgery in the CHU Montpellier or Toulouse

Exclusion Criteria

* The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study
* The subject refuses to sign the consent
* It is impossible to give the subject informed information
* The patient is under safeguard of justice or state guardianship
* The patient is having ambulatory programmed surgery
* The patient has an anesthetic consultation in a different health establishment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Nīmes

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Géraldine Leguelinel-Blache

Role: STUDY_DIRECTOR

CHU Nimes

Locations

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CHU de Montpellier

Montpellier, , France

Site Status

CHU de Nimes

Nîmes, , France

Site Status

CHU de Toulouse

Toulouse, , France

Site Status

Countries

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France

Other Identifiers

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PHRCI/2018/GL-01

Identifier Type: -

Identifier Source: org_study_id

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