Actively Recruiting
The Impact of Intraperitoneal Spray Combined With Intravenous Lidocaine on Postoperative Pain After Myomectomy
Led by General Hospital of Ningxia Medical University · Updated on 2025-12-05
100
Participants Needed
1
Research Sites
72 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to determine whether laparoscopic spraying combined with intravenous injection of lidocaine can improve pain in patients undergoing laparoscopic myomectomy under general anesthesia.
CONDITIONS
Official Title
The Impact of Intraperitoneal Spray Combined With Intravenous Lidocaine on Postoperative Pain After Myomectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 65 years old
- ASA physical status classification I to III
- Scheduled for laparoscopic hysteromyoma (myomectomy) resection under general anesthesia
- Provided informed consent by signing the consent form
You will not qualify if you...
- Surgery expected to last longer than 3 hours
- Need for additional surgery during the procedure
- Allergy to any of the study drugs
- Severe psychological, liver, kidney, or heart diseases
- History of chronic pain or arrhythmia
- Conversion from laparoscopy to laparotomy or change in surgical approach during surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
General Hospital of Ningxia Medical University
Yinchuan, Ningxia, China
Actively Recruiting
Research Team
M
Ma Hanxaing
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
4
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