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Study of Erector Spinae Plane block for postoperative analgesia in cesarean section

A prospective randomised controlled study to determine the effect of bilateral ultrasound- guided Erector Spinae Plane block for postoperative analgesia in cesarean section - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067919
Enrollment
60
Registered
2024-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Sponsors

Dr Benita Abraham
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Undergoing Cesarean Section

Exclusion criteria

Exclusion criteria: Patient refusal to ESPB presence of coagulopathy or bleeding disorder were administered an antiplatelet agent local infection at the injection site hypersensitivity to local amide anesthetics central neuropathy uncontrolled diabetes mellitus significant cardiopulmonary disease, hepatic or renal failure or psychiatric disease. Inability to give consent to the study

Design outcomes

Primary

MeasureTime frame
Visual analog scale (VAS) for painTimepoint: 0 hour, 2 hours , 4hours, 6 hours , 8 hours, 12hours 24 hours and 48 hours

Secondary

MeasureTime frame
Incidence of adverse effectsTimepoint: Number of events in 48 hours;Time for the first request to analgesiaTimepoint: Hours;Total postoperative analgesia Timepoint: 24 hours

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