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Comparison of postoperative analgesia effects between subcostal anterior quadratus lumborum block and tansversus abdominis plane block in bariatric surgery: a prospective randomized controlled study

Comparison of postoperative analgesia effects between subcostal anterior quadratus lumborum block and tansversus abdominis plane block in bariatric surgery: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070556
Enrollment
Unknown
Registered
2023-04-17
Start date
2023-04-17
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

obesity

Interventions

Q group :Subcostal anterior quadratus lumborum block
C group :Abdominal transverse fascial plane block

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18-65 years old, ASA grade II-III, BMI = 30kg/m 2, Patients who plan to undergo laparoscopic weight-loss surgery and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: Abnormal coagulation function, infection/inflammation at puncture site, clear or known history of spinal deformation or spinal surgery, and chronic pain history; Refuse to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
The consumption of opioid at 24 hours after surgery;

Secondary

MeasureTime frame
VAS score for pain during rest/activity;Additional types and doses of analgesic drugs;Incidence and severity of nausea and vomiting (VAS score);Type and dosage of additional antiemetic drugs;PACU time;Postoperative exhaust time;First time getting out of bed activity time;Feeding time of fluid quality;Postoperative hospitalization time;

Countries

China

Contacts

Public ContactBucheng Liao

Peking University Shenzhen Hospital

824345126@qq.com+86 18218417890

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026