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OncoMatch/Clinical Trials/NCT07860203

Stellate Ganglion Block and Dexmedetomidine for Postoperative Sleep in Women Undergoing Laparoscopic Gynecologic Surgery

Official title: Effects of Stellate Ganglion Block Combined With Dexmedetomidine on Postoperative Sleep Quality in Patients Undergoing Laparoscopic Gynecological Surgery: A Randomized Controlled 2×2 Factorial Trial

Is NCT07860203 recruiting? Yes, currently enrolling (Oct 2026). This NA trial studies DEX 0.2 μg/kg/h. for uterine fibroids (leiomyoma).

NARecruitingCatherin ZhangNCT07860203Data as of Oct 2026Location: China

Treatment: DEX 0.2 μg/kg/h. — Study Objectives This study aims to investigate the effects of preoperative stellate ganglion block and intraoperative intravenous dexmedetomidine on postoperative sleep disturbance in patients undergoing laparoscopic gynecologic surgery, with the goals of reducing pain and postoperative adverse reactions and identifying an effective, safe, economical, and broadly applicable intervention strategy that may facilitate emergence from anesthesia, accelerate postoperative recovery, shorten the length of hospital stay, and reduce hospitalization costs. This trial aims to determine whether preoperative stellate ganglion block (SGB) and intraoperative intravenous dexmedetomidine (DEX) can improve postoperative sleep quality in patients undergoing laparoscopic gynecologic surgery, and whether the combination of these two interventions provides an interaction effect or additional ben

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Extracted eligibility criteria

Treatments studied

Other

DEX 0.2 μg/kg/h.

Cancer type

Endometrial Cancer

Cervical Cancer

Ovarian Cancer

Demographics

Ages ≤ 75
Female only

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07860203 currently recruiting?

Yes, this trial is currently recruiting patients.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

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