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Aim To Study The Effect of Pain-relieving Medicine Injected on The Back

A prospective randomised double blinded controlled study evaluating ultrasound guided erector spinae block for post-operative pain relief in paediatric patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023213
Enrollment
60
Registered
2020-02-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

None listed

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: ASA grades I and II Age: 1 yr to 12 yrs Scheduled to undergo elective surgical procedures

Exclusion criteria

Exclusion criteria: Allergy for local anaesthetic ASA III and IV Local infection at injection sites Elective Postoperative ventilation

Design outcomes

Primary

MeasureTime frame
To determine the duration of analgesia with erector spinae blockTimepoint: every second hourly till 12 hours post surgery—

Secondary

MeasureTime frame
Pain score,time at which rescue medication first given and number of rescue medications neededTimepoint: q2h for 12 hours—

Countries

India

Contacts

Public ContactDr Gowri Shankar B

RAINBOW CHILDRENS HOSPITAL

drgowrishankarb@gmail.com9066997742

Outcome results

None listed

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