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Clinical Trials/CTRI/2020/08/026995
CTRI/2020/08/026995Not yet recruitingPhase 1

Comparison of analgesic efficacy of dexamethasone versus dexmedetomidine as an adjuvant to ropivacaine in ultrasound guided transverse abdominis block for postoperative pain relief in caesarean section

Dmch1 site in 1 country100 target enrollmentStarted: May 8, 2020Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Not yet recruiting
Sponsor
Dmch
Enrollment
100
Locations
1
Primary Endpoint
Time to initial postoperative pain and first rescue analgesic.

Study Overview

Brief Summary

Post operative caesarean patients have break through post op pain which will affects mother and baby. So we will give transverse abdominis peroneus block after completion of caesarean section with ropivacaine with dexmedetomidine or dexamethasone and compare the efficacy of dexmedetomidine versus dexamethasone as an adjunct to ropivacaine for post operative pain relief in caesarean section

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Participant and Investigator Blinded

Eligibility Criteria

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

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • •Any contraindication to spinal anesthesia; history of recent opioid exposure; hypersensitivity to any drugs used in study; significant cardiovascular, renal or hepatic diseases and known fetal abnormalities.

Outcomes

Primary Outcomes

Time to initial postoperative pain and first rescue analgesic.

Time Frame: outcome will be assessed immediately after shifting the patient to recovery, every hrly until the patient experience pain with VAS more than 3

Adverse effects if any

Time Frame: outcome will be assessed immediately after shifting the patient to recovery, every hrly until the patient experience pain with VAS more than 3

Secondary Outcomes

  • Time to initial rescue analgesic.(Adverse effects if any)

Investigators

Sponsor
Dmch
Sponsor Class
Private medical college

Study Sites (1)

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