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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04013061
Acronym
PREVEMCA
Enrollment
378
Registered
2019-07-09
Start date
2020-02-25
Completion date
2021-09-30
Last updated
2025-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgical Procedures, Operative

Brief summary

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

Interventions

OTHERPluridisciplinary consultation

Pharmacist-anesthesiologist team will be present during the anesthetic consultation

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Rate of patients with at least one medication error for chronic treatment48 hours post-admission%

Secondary

MeasureTime frameDescription
Rate of medication errors corrected48 hours post-admission%
Rate of prescriptions respecting the Société Française d'Anesthésie et de Réanimation recommendations48 hours post-admission%
Rate of corrected medication errors or major, critical or catastrophic severity according to HAS 201848 hours post-admission%
Nature of medication error48 hours post-admissionAccording to REMED (Revue des Erreurs liées aux Médicaments Et Dispositifs médicaux) classification
Rate of medications not available on the establishment's therapeutic book and not brought by the patient48 hours post-admission%
Duration in hospitalEnd of hospitalization (max 30 days)Days
Rate of delay or cancellation of surgery linked to preoperational medication errorEnd of study (13 months)%
Rate of patients whose usually prescribed medication at admission is not available for them in the evening following surgery48 hours post-admission%

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026