Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06690307
PHASE4

Oxycodone Versus Sufentanil in Patient-controlled Intravenous Analgesia After Laparoscopic Hysterectomy

Sponsor: Affiliated Hospital of Nantong University

View on ClinicalTrials.gov

Summary

This study is designed to evaluate the efficacy and safety of hydrocodone in patient-controlled intravenous analgesia (PCIA) during gynecological laparoscopy, thus to explore suitable PCIA scheme to optimize postoperative pain management for patients undergoing gynecological laparoscopic surgeries.

Official title: The Efficacy and Safety of Oxycodone in Patient-controlled Intravenous Analgesia After Laparoscopic Hysterectomy

Key Details

Gender

FEMALE

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

64

Start Date

2024-12-03

Completion Date

2026-07-31

Last Updated

2024-12-04

Healthy Volunteers

No

Interventions

PROCEDURE

patient controlled intravenous analgesia(PCIA)

Patients will receive sulfentanil for PCIA.

PROCEDURE

patient controlled intravenous analgesia(PCIA)

Patients will receive oxycodone for PCIA.

Locations (1)

Affiliated hospital of Nantong University

Nantong, Jiangsu, China