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Clinical Trials/CTRI/2021/02/030926
CTRI/2021/02/030926
Recruiting
Not Applicable

Comparison of Transversalis Fascia Plane Block versus Transverse Abdominis Plane block for postoperative analgesia in patients undergoing caesarean section: A Randomized controlled trial.

All India institute of Medical Sciences Patna1 site in 1 country64 target enrollmentStarted: February 17, 2021Last updated:
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Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
All India institute of Medical Sciences Patna
Enrollment
64
Locations
1
Primary Endpoint
To assess time to first rescue analgesia after block
OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Overview

Brief Summary

Caesarian section is one of the most commonly done lower abdominal surgeries. Regional Anaesthesia is a part of multimodal analgesia which can be used for lower abdominal surgeries. Transversalis abdominis plane block reduces opioid consumption and patient satisfaction and improves postoperative pain management. Transversalis Fascia plane block is given in the posterior axillary line, which blocks the branches of L1 nerve roots and ilioinguinal and iliohypogastric nerves. Fewer Study  compared Transversalis Fascia plane block  versus transverse abdominis plane block in cesarean section for postoperative analgesia.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 45.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • •ASA I and II
  • •Patients between the ages of 18-45 years.

Exclusion Criteria

  • •1.Patient refusal 2.Coagulopathy /thrombocytopenia 3.Localised infection at the proposed site of injection.
  • •4.Inability to comprehend the scoring systems to be employed due to physical or mental problems 5.Known allergy to the drugs to be used (local anaesthetics, opioids) 6.Opioid tolerance /dependence 7.Renal/hepatic impairment 8.Known cardio respiratory impairment 9.Patient with any neurological disorder.

Outcomes

Primary Outcomes

To assess time to first rescue analgesia after block

Time Frame: time to first rescue analgesia after block

Secondary Outcomes

  • •Compare pain using the Numerical Rating Score (NRS) at 0, 30 min, 1 hr, 6 hr, 12 hr and 24 hrs post-surgery.(•To compare the total opioid consumption in 24 hours.)

Investigators

Sponsor
All India institute of Medical Sciences Patna
Sponsor Class
Government medical college

Study Sites (1)

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