Skip to content

Effect of preoperative sham feeding combined with stellate ganglion block on postoperative gastrointestinal function recovery in patients undergoing laparoscopic gynecological surgery— A prospective randomized clinical trial

Effect of preoperative sham feeding combined with stellate ganglion block on postoperative gastrointestinal function recovery in patients undergoing laparoscopic gynecological surgery— A prospective randomized clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073715
Enrollment
Unknown
Registered
2023-07-19
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postperative gastriontestinal dysfunction

Interventions

Control group:None
Chewing gum group:Chew gum for at least 30 minutes before entering the operating room
Stellate ganglion block group:30 minutes before induction of anesthesia, perform right SGB under ultrasound guidance, and inject 0.5% ropivacaine 4ml into the root of the anterior tubercle of C6 trans
Chewing gum combined with Stellate ganglion block group:Chewing gum for at least 30 minutes before entering the operating room and 30 minutes before induction of anesthesia, perform right SGB under ul

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Elective laparoscopic gynecological surgery 2. ASA I~II 3. Age 18-60 years old 4. Sign the informed consent

Exclusion criteria

Exclusion criteria: 1. There are related puncture contraindications (coagulation dysfunction; local skin ulceration infection; local anesthetic allergy; asthma; glaucoma, etc.) 2. Those with a history of neck surgery 3. Recent long-term use of sedatives, antidepressants, anti-inflammatory drugs 4. Recently underwent SGB treatment; 5. BMI = 28 kg/m²; 6. People without chewing ability; 7. Previous history of diseases or surgeries that lead to digestive disorders; 8. Have taken gastrointestinal motility drugs within 72 hours before the operation; 9. People with mental and nervous system diseases and disturbance of consciousness; 10. Persons with limited educational

Design outcomes

Primary

MeasureTime frame
Postoperative first exhaust time;

Secondary

MeasureTime frame
Postoperative first bowel movement time;Postoperative first oral intake time;QoR-15 score at 24, 48, and 72 hours after operation;NRS score at 24, 48, and 72 hours after operation;I-FEED score at 24, 48, and 72 hours after operation;Analgesic dosage;

Countries

China

Contacts

Public ContactJindong Liu

Affiliated Hospital of Xuzhou Medical University

liujindong1818@163.com+86 139 5135 5136

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026