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Clinical Trials/CTRI/2021/02/031289
CTRI/2021/02/031289Not yet recruitingNot Applicable

Comparison of quadratus lumborum block, erector spinae plane block and transversus abdominis plane block for post cesarean section analgesia: A prospective randomized clinical trial.

Dr Aman Malawat1 site in 1 country300 target enrollmentStarted: February 21, 2021Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
300
Locations
1
Primary Endpoint
To compare time of first rescue analgesic needed.
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of this study is to compare the analgesic efficacy of quadratus lumborum block, erector spinae plane block and TAP block in patients who had cesarean section under spinal anesthesia

Study Design

Study Type
Interventional
Allocation
Not Applicable
Masking
Participant, Investigator and Outcome Assessor Blinded

Eligibility Criteria

Ages
20.00 Year(s) to 35.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • •Patient with ASA Class II, III
  • •Normal singleton pregnancy with a gestation of at least 37 weeks
  • •Patient’s written and informed consent.

Exclusion Criteria

  • •Patient with ASA Class IV & V
  • •Patient refusal
  • •Local infection at the site of injection
  • •Allergy to study medications
  • •Anatomic abnormalities
  • •Inability to comprehend or participate in pain scoring system.

Outcomes

Primary Outcomes

To compare time of first rescue analgesic needed.

Time Frame: baseline

Secondary Outcomes

  • To compare the total cumulative dose of analgesic needed in first 48 hours after surgery.(48 hours)
  • To compare severity of postoperative pain via visual analogue pain scale at rest (VASR) and with movement (dynamic)(48 hours)

Investigators

Sponsor
Dr Aman Malawat
Sponsor Class
Other [self]

Study Sites (1)

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