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Effect of sheath of rectus abdominis block combined with transverse plane block on the condition in laparoscopic gynecological surgery

Effect of RSB with TAPB on the condition in laparoscopic gynecological surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026767
Enrollment
Unknown
Registered
2019-10-21
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-10-28

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

Conditions

the condition of laparoscopic gynecological surgery

Interventions

experimental group:RSB and TAPB combined with moderated muscle-relaxing
control group:moderate muscle-relaxing

Sponsors

Tongji Hospital Affiliated to Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I~ II; 2. aged 18-55 years; 3. BMI 19 ~ 23kg/m2; 4. laparoscopic total hysterectomy and bilateral adnexectomy and/or pelvic lymphadenectomy under elective general anesthesia lasted for more than 2 hours; 5. informed consent has been signed.

Exclusion criteria

Exclusion criteria: 1. the patient had history of abdominal surgery;Patients with preoperative or intraoperative confirmed distant tumor metastasis: abdominal implant, distant lymph node metastasis, liver or other organ metastasis, etc. 2. according to researchers like professional athletes and weight trainers, abdominal muscle tension can be changed through strength training;Need to use wheelchair, crutches and other lower limbs mobility, physical weakness;Back and spine injuries, infections, deformities and other conditions where nerve block is not possible; 3. allergic to any of the drugs used in the experiment; 4. pregnant or lactating women; 5. patients with severe mental and neurological symptoms cannot cooperate with the study; 6. those who participated in other clinical trials within 3 months before being enrolled in the study; 7. the researcher believes that other reasons are not suitable for clinical trials; 8. patients who have changed their surgical methods or received only palliative surgical treatment; 9. patients with abnormal coagulation function; 10. patients who cannot cooperate.

Design outcomes

Primary

MeasureTime frame
Surgeon visual field satisfaction (5-point scale);

Countries

China

Contacts

Public ContactZhang Yi

Tongji Hospital Affiliated to Huazhong University of Science and Technology

doc_zhang18@163.com+86 13986039131

Outcome results

None listed

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