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A study of quality and duration of analgesia in ultrasound guided erector spinae plane block for paediatric thoracotomy

A prospective observational study of quality and duration of analgesia with 0.25% bupivacaine in ultrasound guided erector spinae plane block for paediatric thoracotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/01/022703
Enrollment
30
Registered
2020-01-10
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: J949- Pleural condition, unspecified

Interventions

None listed

Sponsors

Dr Tejaswini C Jambotkar
Lead Sponsor
Dr Anila Malde
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Paediatric patients between 1-12 years undergoing thoracotomy.

Exclusion criteria

Exclusion criteria: Infection at local site of block Parental refusal Inability to assess postoperative pain due to any reasons.

Design outcomes

Primary

MeasureTime frame
To evaluate quality of analgesia using changes in haemodynamic parameters as a surrogate marker intraoperatively. To evaluate quality of postoperative analgesia using pain scores. To note the duration of analgesia.Timepoint: Baseline, 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 6 hours, 8 hours—

Secondary

MeasureTime frame
To study adverse effects, if any Timepoint: Within 24 hours.—

Countries

India

Contacts

Public ContactDr Tejaswini C Jambotkar

Lokmanya Tilak Municipal Medical College and General Hospital, Sion, Mumbai.

drtejaswini.jambotkar@gmail.com8793309308

Outcome results

None listed

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