Skip to main content
Clinical Trials/CTRI/2025/08/092513
CTRI/2025/08/092513
Not yet recruiting
Phase 3

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

Monika Yadav1 site in 1 country110 target enrollmentStarted: September 1, 2025Last updated:

Overview

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Monika Yadav
Enrollment
110
Locations
1
Primary Endpoint
The time to request the first post-operative rescue analgesic dose

Overview

Brief Summary

This study is a randomized, double blind, parallel group, single-centre trial comparing the efficacy of ultrasound-guided erector spinae plane block versus local wound infiltration for post-operative analgesia in patients undergoing video-assisted thoracoscopic surgery in 110 patients in a tertiary care centre in India. The primary outcome measure will be to determine the time to request the first post-operative rescue analgesic dose. The secondary outcomes will be total post-operative rescue analgesic requirement, comparison of quality of recovery, incidence of nausea and vomiting in the first 24 hours post-operatively and numerical rating score at rest and during coughing, comparison of sedation scores at 6, 12, and 24 hours post-operatively

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Informed and written consent ASA physical status 1 and 2 Elective video-assisted thoracoscopic surgery.

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.

Outcomes

Primary Outcomes

The time to request the first post-operative rescue analgesic dose

Time Frame: The time point at which the patient requests the first post-operative rescue analgesic dose in first 24 hours.

Secondary Outcomes

  • Total post-operative rescue analgesic requirement(24 Hours post-operatively)
  • Numerical rating score at rest and during coughing(6 ,12 and 24 Hours post-operatively)
  • Comparison of quality of recovery(24 Hours post-operatively)
  • Comparison of sedation scores(6,12, and 24 Hours post-operatively)
  • Incidence of nausea and vomitting(Post-operative period for 24 Hours)

Investigators

Sponsor
Monika Yadav
Sponsor Class
Other [individual]
Responsible Party
Principal Investigator
Principal Investigator

Monika Yadav

Medanta -The Medicity

Study Sites (1)

Loading locations...

Similar Trials