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NCT05540977

Donepezil Prevents Urinary Retention After Extensive Total Hysterectomy

Status unknown EARLY_PHASE1 Last updated 15 September 2022
What this trial tests

EARLY_PHASE1 trial testing Donepezil in Urinary Retention After Procedure in 108 participants. Status unknown.

Timeline
1 August 2022
Primary endpoint
31 May 2023
15 July 2023

Quick facts

Lead sponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen University
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment108
Start date1 August 2022
Primary completion31 May 2023
Estimated completion15 July 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Who can join

Adults 18 to 80, female only, with Urinary Retention After Procedure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Patients were randomly divided into experimental group and control group. The control group received routine postoperative treatment, while the experimental group took donepezil 5mg orally before going to bed every night from the first day after surgery. The catheter was removed and residual urine was measured in both groups 14 days after surgery, the catheter was successfully removed when the residual urine was less than 100ml. After 14 days, the patient was returned to the hospital for residual urine test, and the residual urine was repeated until the residual urine volume was less than or equal to 100ml. The incidence of postoperative urinary retention and adverse drug reactions were compared between the two groups.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Donepezil

Trials testing the same drug.

Other recruiting trials for Urinary Retention After Procedure

Currently open trials in the same condition.

Other Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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