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A randomized controlled, double-blind trial of ultrasound-guided erector spinae plane block for postoperative analgesia in patients undergoing laparoscopic cholecystectomy

A randomized controlled, double-blind trial of ultrasound-guided erector spinae plane block for postoperative analgesia in patients undergoing laparoscopic cholecystectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039019
Enrollment
Unknown
Registered
2020-10-13
Start date
2020-10-19
Completion date
Unknown
Last updated
2021-01-11

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

Conditions

Laparoscopic cholecystectomy

Interventions

Experimental group:drug block
control group: placebo block

Sponsors

Leshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The age is 18-70 years old, no gender limit; 2. Patients who plan to undergo LC and require postoperative analgesia; 3. American Society of anesthesiologists (ASA) grade I ~ II; 4. The users who have no communication barriers and can cooperate with the implementation and understanding of relevant scales; 5. The subjects participated voluntarily and informed consent was signed.

Exclusion criteria

Exclusion criteria: 1. Contraindications of nerve block (such as infection of puncture site); 2. Preoperative examination of tumor patients indicated that the tumor had metastasis; 3. Severe liver and kidney diseases, coagulation dysfunction, etc; 4. Previous history of abdominal surgery or trauma; 5. Long term use of sedative and analgesic drugs or alcohol, sedative and analgesic drug addicts.

Design outcomes

Primary

MeasureTime frame
VAS score;Is there any shoulder pain involved;Patient satisfaction with postoperative analgesia;First aid analgesia time after operation;Times of emergency analgesia within 48 hours after operation;Total requirement of first aid analgesia within 48 hours after operation;Time of first ambulation;First exhaust time;

Secondary

MeasureTime frame
Operation time;Intraoperative blood loss;Additional dose of sufentanil during operation;Postoperative hospital stay;

Countries

China

Contacts

Public ContactHeng Lu

Leshan People's Hospital

244758947@qq.com+86 18608071323

Outcome results

None listed

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