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Effects of general anesthesia combined with ultrasound guided T12 and L2 erctor spinae plane block on surgical field and postoperative pain in laparoscopic gynecological surgery.

Effects of general anesthesia combined with ultrasound guided T12 and L2 erctor spinae plane block on surgical field and postoperative pain in laparoscopic gynecological surgery.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024204
Enrollment
Unknown
Registered
2019-06-30
Start date
2019-10-20
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Anesthesia for patients undergoing laparoscopic gynecologic surgery

Interventions

Sponsors

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

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) ASA grades 1 to 2; (2) aged 18-55 years; (3) BMI 18.5 ~ 24kg/m2; (4) selective patients undergoing Laparoscopic whole uterus and double appendages and(or) lymphadenectomy under general anesthesia (5) informed consent has been signed.

Exclusion criteria

Exclusion criteria: (1) the patient had a history of abdominal surgery; (2) patients with confirmed distant tumor metastasis before or during surgery: intraperitoneal implantation, distant lymph node metastasis, liver or other organ metastasis, etc.; (3) the operation time is less than 2 hours; (4) researchers such as professional athletes and weight trainers believe that abdominal wall muscle tension can be changed through strength training; (5) use wheelchairs, crutches and other lower limbs for mobility and physical weakness; (6) back and spine trauma, infection, deformity and other conditions that cannot be blocked; (7) allergic to any of the drugs used in the experiment; (8) pregnant or lactating women; (9) patients with severe psychiatric and neurological symptoms who are unable to cooperate with the study; (10) participated in other clinical trials within 3 months prior to study inclusion; (11) the researchers believe that other reasons are not suitable for clinical trials; (12) subjects who change their surgical methods or only receive palliative surgical treatment; (13) patients with abnormal coagulation function; (14) patients who cannot cooperate.

Design outcomes

Primary

MeasureTime frame
Physician vision satisfaction score;

Secondary

MeasureTime frame
Postoperative pain score and use of analgesics;Postoperative complications and recovery time nodes (including first time out of bed, exhaust time, discharge time, etc.);Time of extubation (min) = time from the end of operation to the removal of endotracheal tube (TOF=0.9);

Countries

China

Contacts

Public ContactZhang Yi

Tongji Hospital Affiliated to Tongji Medical College, 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