Analgesic Efficacy of Ultrasound-guided Bilateral Costal Margin Block in Laparoscopy-assisted Gastrectomy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100043873

Enrollment

Unknown

Registered

2021-03-04

Start date

2021-03-05

Completion date

Unknown

Last updated

2022-10-24

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

Conditions

gastric cancer

Interventions

Intervention group:standard general anesthesia with ultrasound-guided bilateral costal margin block

Control group:only received standard general anesthesia.

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Eligible patients were 18-75 yr old with ASA physical status 1-2 and scheduled for elective laparoscopy-assisted gastrectomy.

Exclusion criteria

Exclusion criteria: A history of relevant drug allergy, body mass index (BMI) >= 30 kg/m2 or <= 15kg/m2, a history of alcohol or analgesics dependence, history of upper abdominal surgery, local infection at the site of injection or systemic infection, peripheral neuropathy, coagulopathy, difficulty with communication, and unable to obtain informed consent.

Design outcomes

Primary

Measure	Time frame
24h intravenous morphine consumption after surgery;	—

Secondary

Measure	Time frame
0-6h, 6-12h, 12-24h, 24-48h intravenous morphine consumption;NRS pain scores;time to first opioid rescue analgesia;patient satisfaction with pain relief during two days postoperatively;time to first ambulation;Time to first flatus;hospital length of stay;	—

Countries

China

Contacts

Public ContactWeijian Wang

The First Affiliated Hospital of Wenzhou Medical University

wangwj2002@163.com+86 13806683232

Outcome results

None listed

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