Ultrasound-guided Subcostal Transversus Abdominis Plane Block Versus Bilateral Erector Spinae Block For Laparoscopic Inguinal Hernia Repair -Randomised Controlled Triple binded Trial

Ultrasound-guided Subcostal Transversus Abdominis Plane Block Versus Bilateral Erector Spinae Block For Laparoscopic Inguinal Hernia Repair -A Comparative Randomized Triple -blinded Clinical Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/076140

Enrollment

Registered

2024-11-01

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: 20ml of0.25% Bupivacaine on each side in Subcostal Transversus Abdominis Plane Block: Participants in this group undergoing Laparoscopic Inguinal Hernia Repair surgeries get both sides

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 & 2 Patients with Age 18-65yrs Patients who are willing

Exclusion criteria

Exclusion criteria: ASA 3 & 4 Patients with cardiac, respiratory, kidney or liver diseases and chronic drug users Patients with BMI more than 35 Patients with hypersensitivity to one of the medications used

Design outcomes

Primary

Measure	Time frame
1.To compare Total analgesic requirement upto 24hr after surgery 2.Degree of pain assessed by VNRS upto 24hrs after surgery 3.Any Intraoperative or postoperative problems upto 24hrs to be managedTimepoint: 1.To compare Total analgesic requirement upto 24hr after surgery upto 24hrs after surgery 2.Degree of pain assessed by VNRS upto 24hrs after surgery 3.Any Intraoperative or postoperative problems upto 24hrs to be managed	—

Measure

Time frame

1.To compare Total analgesic requirement upto 24hr after surgery 2.Degree of pain assessed by VNRS upto 24hrs after surgery 3.Any Intraoperative or postoperative problems upto 24hrs to be managedTimepoint: 1.To compare Total analgesic requirement upto 24hr after surgery upto 24hrs after surgery 2.Degree of pain assessed by VNRS upto 24hrs after surgery 3.Any Intraoperative or postoperative problems upto 24hrs to be managed

—

Secondary

Measure	Time frame
1.Fentanyl consumption used Intraoperatively till surgery end time. 2.Time for first analgesic request postoperatively within 24hrs after surgeryTimepoint: The secondary outcome is the Fentanyl consumption used Intraoperatively & the time it takes for the first analgesic request postoperatively after surgery upto 24hrs	—

Countries

India

Contacts

Public ContactDr.Rajesh Kumar Kodali

Sri Ramachandra Institute of Higher Education And Research

vrajesh.kodali@gmail.com9962398266

Outcome results

None listed

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