RecruitingNot Applicable

The Impact of Intraperitoneal Spray Combined With Intravenous Lidocaine on Postoperative Pain After Myomectomy

China100 participantsStarted 2024-08-01

Plain-language summary

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.

Who can participate

Age range18 Years – 65 Years

SexFEMALE

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Inclusion criteria

✓. Age:18-65 years old;
✓. ASA physical status classification I - III;
✓. Undergoing laparoscopic hysteromyoma resection under general anesthesia;
✓. The patient has been informed and has signed the informed consent form.

Exclusion criteria

✕. Surgery duration exceeding 3 hours;
✕. Need for additional surgery;
✕. Allergy to the study drugs;
✕. Presence of severe psychological,hepatic,renal,and cardiac diseases;
✕. History of chronic pain or arrhythmia.
✕. The patient or their family withdraws from or refuses to participate in the trial during the observation period;
✕. Conversion from laparoscopy to laparotomy or change in surgical approach during the procedure.

What they're measuring

The incidence rate of moderate to severe pain within 24 hours

Timeframe: Within 24 hours after surgery

Trial details

NCT IDNCT07268495

SponsorGeneral Hospital of Ningxia Medical University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-08-01

Contact for this trial

Ma Hanxaing

86-13519591508 mahanxiang@hotmail.com

View on ClinicalTrials.gov More Postoperative Pain trials