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A study comparing erector spinae block and surgical site local anaesthetic infiltration for pain relief after minimally invasive lung surgery

Comparison of efficacy of ultrasound- guided erector spinae plane block versus local wound infiltration for post-operative analgesia in patients undergoing video-assisted thoracoscopic surgery: a double blind randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092513
Enrollment
110
Registered
2025-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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: Erector spinae plane block: Ultrasound-guided erector spinae block will be administered as single dose at T5 vertebral level with 40 ml of 0.2% Ropivacaine between T5 vertebral level an

Sponsors

Monika Yadav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Informed and written consent ASA physical status 1 and 2 Elective video-assisted thoracoscopic surgery

Exclusion criteria

Exclusion criteria: Patient refusal Infection at the site Chronic pain patients or patients with analgesic dependence INR more than 1.5 Difficulty in understanding or non-compliance with the quality of recovery questionnaire

Design outcomes

Primary

MeasureTime frame
The time to request the first post-operative rescue analgesic doseTimepoint: The time point at which the patient requests the first post-operative rescue analgesic dose in first 24 hours.

Secondary

MeasureTime frame
Total post-operative rescue analgesic requirementTimepoint: 24 Hours post-operatively;Numerical rating score at rest and during coughingTimepoint: 6 ,12 and 24 Hours post-operatively;Comparison of quality of recoveryTimepoint: 24 Hours post-operatively;Comparison of sedation scoresTimepoint: 6,12, and 24 Hours post-operatively;Incidence of nausea and vomittingTimepoint: Post-operative period for 24 Hours

Countries

India

Contacts

Public ContactMonika Yadav

Medanta -The Medicity

yadavmonika248@gmail.com9518089485

Outcome results

None listed

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