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Series studies of the efficacy of ultrasound-guided ilioinguinal/iliohypogastric nerve block for inguinal hernia repair under local anesthesia

Series studies of the efficacy of ultrasound-guided ilioinguinal/iliohypogastric nerve block for inguinal hernia repair under local anesthesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056670
Enrollment
Unknown
Registered
2022-02-10
Start date
2023-09-04
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

Inguinal hernia

Interventions

Part I-No block group:No block
Part I-Ilioinguinal/iliohypogastric nerve block group:Ilioinguinal/iliohypogastric nerve block before surgery
Part II-Ilioinguinal/iliohypogastric nerve block group:Ilioinguinal/iliohypogastric nerve block before surgery
Part II-Quadratus lumborum block group:Quadratus lumborum block group before surgery

Sponsors

Department of Anesthesiology, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years; 2. ASA classification I-III; 3.18kg/?=BMI=30kg/? 4. Unilateral Gilbert inguinal hernia tension-free repair is proposed; 5. Sign the informed consent form for research.

Exclusion criteria

Exclusion criteria: 1. strangulated hernia and incarcerated hernia; 2. There is contraindication of nerve block or study drug; 3. Coagulation dysfunction; 4. Patients with high bleeding risk; 5. Serious liver and kidney dysfunction; 6. Patients with chronic pain or chronic opioid use; 7. Communication barrier, unable to cooperate with intervention implementation or understand the use of pain scale; 8. Patients have participated in other clinical trials within three months.

Design outcomes

Primary

MeasureTime frame
NRS scores at preperitoneal space dissociation ;

Secondary

MeasureTime frame
NRS at postoperative 6h?12h?24h?48h and 3m at rest and during mobilization;Peri-operative dosage of sufentanil and dezoncine;Duration of surgery;Length of hospital stay;Surgeon and patient satisfaction;Incidence of chronic pain at 3 months postoperatively;Operation time of nerve block;Onset time of nerve block;

Countries

China

Contacts

Public ContactFei Liu

West China Hospital, Sichuan University

30333870@qq.com+86 189 8060 5856

Outcome results

None listed

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