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The application of laparoscopic-assisted transversus abdominis plane block in analgesia for laparoscopic inguinal hernia repair

The application of laparoscopic-assisted transversus abdominis plane block in analgesia for laparoscopic inguinal hernia repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122800
Enrollment
Unknown
Registered
2026-04-17
Start date
2026-04-17
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

indirect inguinal hernia,direct inguinal hernia

Interventions

General anesthesia + laparoscopic-assisted TAPB group:Laparoscopic-assisted transversus abdominis plane block
Control group:General anesthesia

Sponsors

Pinggu District Hospital, Beijing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18 - 80 years old, gender not restricted; 2. ASA classification: I - III; 3. No use of drugs affecting the nervous system before the operation, no history of chronic pain before the operation; 4. Signed the informed consent form; 5. Diagnosed with inguinal hernia and selected laparoscopic inguinal hernia repair surgery.

Exclusion criteria

Exclusion criteria: 1. Body mass index (BMI) > 35kg/m^2; 2. Patients allergic to ropivacaine; 3. Patients with cognitive decline, communication disorders, and inability to accurately express pain scores; 4. Patients with coagulation dysfunction; 5. Patients with severe bronchial asthma, coronary heart disease, hypertension, or diabetes; 6. Patients with infected puncture sites; 7. Patients who received analgesic drugs that affected the result assessment before the operation.

Design outcomes

Primary

MeasureTime frame
Pain visual analogue score at 24 hours post-operation (+/- 1 hour);

Secondary

MeasureTime frame
The time of the first postoperative defecation;Incidence of postoperative adverse reactions.;The time from the end of the surgery to the first time getting out of bed;Overall comfort and satisfaction 24 hours after the surgery;Postoperative analgesic drug dosage;Pain visual analogue score at 2 hours (+/- 0.5 hours), 6 hours (+/- 0.5 hours), 12 hours (+/- 0.5 hours), and 48 hours (+/- 1 hour) after surgery;The dosage of anesthetic drugs (propofol, remifentanil) used during the operation;

Countries

China

Contacts

Public ContactLv Yanpeng

Pinggu District Hospital, Beijing

dapeng91221@163.com+86 15611765082

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026