Erector spinae block for pain relief

Effects of erector spinae block on the postoperative quality of recovery after Gender Reassignment chest surgeries: a prospective randomized double-blinded study - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/064389

Enrollment

Registered

2024-03-19

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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: Ropivociane in erector spinae block: to see the efficacy. total duration of 24 hours followed up for the effective block. Control Intervention1: Intraoperative blocks: Erector spinae bl

Eligibility

Inclusion criteria

Inclusion criteria: Both sexes and for transfeminine surgeries

Exclusion criteria

Exclusion criteria: not willing for injections

Design outcomes

Primary

Measure	Time frame
first onset of pain, rescue analgesiaTimepoint: pain assessed at time intervals like 2, 4, 6,8,12 and 24 hours after the block	—

Secondary

Measure	Time frame
complications for the procedureTimepoint: at intervals in 4, 8, 12 & 24 hours noted. after rescue analgesia	—

Countries

India

Contacts

Public ContactDr Krishna Prasad T

Shri Sathya Sai Medical College

drkrishna86@gmail.com09944579455

Outcome results

None listed

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