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To check the effectiveness of injection given in the back called erector spinae plane, in patients undergoing operation for hernia, under spinal anaesthesia where only legs and part of the abdomen will be made numb

Efficacy of erector spinae plane block on post-operative pain in patients undergoing inguinal hernia repair under subarachnoid block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/052024
Enrollment
60
Registered
2023-04-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: Efficacy of erector spinae plane block for post operative pain in patients undergoing inguinal hernia repair under subarachnoid block: USG guided erector spinae plane block at level of

Sponsors

Pt BD Sharma University Of Health Sciences, PGIMS, ROHTAK, HARYANA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients

Exclusion criteria

Exclusion criteria: History of allergy and known hypersensitivity to local anaesthetic agents, history of bleeding disorders, patients on anticoagulants, history of neuropathic disease, morbid obesity, patient with psychiatric illness

Design outcomes

Primary

MeasureTime frame
To evaluate VAS score to assess postoperative analgesia in open inguinal hernia repair patientsTimepoint: To evaluate VAS score in postoperative period at 0, 1, 2, 6, 12 and 24 hours—

Secondary

MeasureTime frame
Time to first analgesic demand, 24 hour analgesic consumption, to note complications,if any and patient satisfaction with post-operative pain reliefTimepoint: Time to first analgesic demand, 24 hour analgesic consumption, to note complications,if any and patient satisfaction with post-operative pain relief—

Countries

India

Contacts

Public ContactDr Nancy Rathi

PGIMS Rohtak

nancyrathee7@gmail.com8607733624

Outcome results

None listed

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