Skip to content

Anterior Quadratus Lumborum Block at Lateral Supra-Arcuate Ligament vs Anterior Quadratus Lumborum Block for Postoperative Recovery after Laparoscopic Cholecystectomy: a double-blind, randomized controlled trial.

Anterior Quadratus Lumborum Block at Lateral Supra-Arcuate Ligament vs Anterior Quadratus Lumborum Block for Postoperative Recovery after Laparoscopic Cholecystectomy: a double-blind, randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088201
Enrollment
Unknown
Registered
2024-08-13
Start date
2024-08-15
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

gallbladder disorders

Interventions

Anterior Quadratus Lumborum Block:Anterior Quadratus Lumborum Block
Anterior Quadratus Lumborum Block at Lateral Supra-Arcuate Ligament:Anterior Quadratus Lumborum Block at Lateral Supra-Arcuate Ligament

Sponsors

Nanchong Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: They are between 18 and 65 years old 2: The ASA classification is grade I - II 3: BMI18-30 4: The quality of recovery questionnaire could be performed after surgery 5: Patients undergoing laparoscopic cholecystectomy 6: Informed consent is signed by all study participants

Exclusion criteria

Exclusion criteria: 1: Allergies to the drugs used in the study 2: There are contraindications to nerve block 3: There are contraindications in the use of drugs used in the trial 4: Have a history of severe cardiovascular and cerebrovascular diseases 5: Alcohol and substance addiction, mental and neurological disorders 6: A history of thoracic or spinal surgery 7: Patients who used any analgesic in the 24 hours before surgery 8: Operation time > 2h 9: Laparotomy was performed during the operation 10: Refused to participate in the trial or was unable to cooperate with the recovery quality score questionnaire

Design outcomes

Primary

MeasureTime frame
qor-15 24 hours after surgery;

Secondary

MeasureTime frame
qor-15 score 48 hours after surgery;NRS scores after surgery;The amount and cases of postoperative analgesia supplemented with tramadol;Block operation time;Block onset time;Number of blocked segments 5 and 15 minutes after block;Incidence of intraoperative hypotension and sinus bradycardia;Time for first rescue analgesia;Occurrence of adverse events;Add the amount and number of tramadol hydrochloride;

Countries

China

Contacts

Public ContactYing Xie

Nanchong Central Hospital

475153895@qq.com+86 159 8377 6950

Outcome results

None listed

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