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Ultrasound-guided Subcostal Transversus Abdominis Plane Block Combined with Calot Triangle Block: Postoperative Analgesic Effect in Laparoscopic Cholecystectomy

Ultrasound-guided Subcostal Transversus Abdominis Plane Block Combined with Calot Triangle Block: Postoperative Analgesic Effect in Laparoscopic Cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125866
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-10
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Post-cholecystectomy pain

Interventions

Transversus Abdominis Plane Block + Calot's Triangle Block:Transverse abdominis plane block with 20 mL of 0.375% ropivacaine, Inject 10 mL of 0.375% ropivacaine into the triangle of Calot area
Transversus Abdominis Plane Block:Transverse abdominis plane block with 20 mL of 0.375% ropivacaine

Sponsors

Beijing General Aerospace Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years old; 2. Body Mass Index (BMI) ranging from 18.5 to 25 kg/m^2; 3. American Society of Anesthesiologists (ASA) physical status classification Grade I to II; 4. Clear consciousness and capable of cooperating to complete VAS pain score, postoperative follow-up and relevant data filling.

Exclusion criteria

Exclusion criteria: 1. Individuals with a clear history of allergy to local anesthetics; 2. Individuals with coagulation dysfunction; 3. Individuals with a history of chronic pain or long-term use of analgesic/sedative drugs (which may interfere with pain scoring and assessment of analgesic effects); 4. Individuals with mental disorders or cognitive impairment (unable to cooperate with study-related assessments); 5. Individuals with a history of abdominal surgery or severe abdominal adhesions (which may affect block procedures and surgical progress); 6. Individuals with uncontrolled underlying diseases such as liver or kidney dysfunction, cardiovascular disease, etc. (which may increase anesthesia and surgical risks).

Design outcomes

Primary

MeasureTime frame
Visual analogue scale pain scores at different time points after surgery;

Secondary

MeasureTime frame
Postoperative patient's time to get out of bed and move around;15-item recovery quality score at preoperative and postoperative 12 hours;

Countries

China

Contacts

Public ContactWang Lei

Beijing General Aerospace Hospital(731 Hospital of China Aerospace Science and Industry Corporation)

156350565@qq.com+86 134 0027 8188

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026