The Efficacy and Safety of Oxycodone in Patient-controlled Intravenous Analgesia After Laparoscopic Hysterectomy
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 4
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.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:
• selective laparoscopic hysterectomy
• general anesthesia
• ASA classification I - III
• aged 18 - 65 years
Locations
Other Locations
China
Affiliated hospital of Nantong University
RECRUITING
Nantong
Contact Information
Primary
Siyuan Liu, PhD
tdfylsy@ntu.edu.cn
+86-85050301
Time Frame
Start Date: 2024-12-03
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 64
Treatments
Active_comparator: sulfentanil group
Participants in the active comparator group will receive sulfentanil for PCIA.
Experimental: oxycodone group
Participants in the experimental group will receive oxycodone for PCIA.
Related Therapeutic Areas
Sponsors
Leads: Affiliated Hospital of Nantong University