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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05237557
Other study ID # 2022-00202
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 9, 2020
Est. completion date December 1, 2021

Study information

Verified date February 2022
Source University of Lausanne Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Single-center, open label, randomized controlled trial of a preoperative nursing dialogue in patient undergoing major visceral surgery aiming in evaluating its impact on patients' anxiety, satisfaction and early postoperative outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date December 1, 2021
Est. primary completion date June 29, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient undergoing elective major visceral surgery - Hospitalization the day before surgery - Sufficient command of French language Exclusion Criteria: - emergency procedures (after unplanned admission) - inability to obtain informed consent or refusal - inability to follow intervention

Study Design


Intervention

Behavioral:
Preoperative nurse dialogue
Performance of a preoperative nurse dialogue prior major visceral surgery

Locations

Country Name City State
Switzerland Department of Visceral Surgery, University Hospital CHUV, Lausanne Lausanne

Sponsors (1)

Lead Sponsor Collaborator
Nicolas DEMARTINES

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Preoperative anxiety State-Trait Anxiety Inventory Form Y (STAI-Y) 5-10 minutes after intervention
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