NCT06429605View on ClinicalTrials.gov

Evaluating the Efficacy and Safety of Preoperative Administration of Duloxetine for Pain Management in Women Undergoing Hysterectomy Via Vaginal Route

NACompletedINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

May 20, 2024

Primary Completion Date

December 25, 2024

Study Completion Date

December 27, 2024

Conditions
Vaginal HysterectomyPostoperative PainvNOTES
Interventions
DRUG

duloxetine

In addition to our standard clinical protocol, study patients were administered 60 mg oral duloxetine 2 hours before surgery and 24 hours after surgery

Trial Locations (1)

35460

Mugla Education and Research Hospital, Muğla

All Listed Sponsors
lead

Erzincan Military Hospital

OTHER

NCT06429605 - Evaluating the Efficacy and Safety of Preoperative Administration of Duloxetine for Pain Management in Women Undergoing Hysterectomy Via Vaginal Route | Biotech Hunter | Biotech Hunter