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Clinical Trials/CTRI/2025/12/099343
CTRI/2025/12/099343Not yet recruitingNot Applicable

Single blind randamized control trial comparing injection bupivacaine with dexamethasone versus injection bupivacaine with dexmedetomidine in suprainguinal fascia iliaca block for postoperative pain relief in fracture hip surgery

MIMER Medical College1 site in 1 country40 target enrollmentStarted: January 1, 2026Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
postoperative pain intensity and duration of analgesia with time of first rescue analgesic requirment.

Study Overview

Brief Summary

Patients posted for proposed study will be diploid in the randomized pattern Total of 40 patients will be divided in 2 groups,20 patients in each group. Group DI: Dexamethasone group will receive 8 mg of Inj .Dexamethasone as adjuvant to Inj. Bupivacaine 0.25%

Group DII: Dexmedetomidine group will receive 50 mcg of Inj.Dexmedetomidine as adjuvant to Inj.Bupivacaine 0.25%.

Study implications:

This study will compare the efficacy of Dexamethasone and Dexmedetomidine as an adjuvant to bupivacaine in Suprainguinal fascia Iliaca block for post-operative analgesia in terms of its duration and Intensity. It also highlights its effect on hemodynamic stability.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients undergoing hip surgery under spinal anaesthesia ASA Grade I and II.

Exclusion Criteria

  • Patients not willing to participate in study with due consent.
  • Drug allergy to Dexmedatomidine -Patients on B blocker,Heart block -Patients with Psychiatric disorder -Severe cardio-pulmonary disease -severe hepatic,renal disease -Neuromuscular disease.

Outcomes

Primary Outcomes

postoperative pain intensity and duration of analgesia with time of first rescue analgesic requirment.

Time Frame: time of first rescue analgesic requirment.

Secondary Outcomes

  • haemodynamic parameteres,sedation score,total amount of analgesic requirement in first 24 hours(24 hours postoperative period)

Investigators

Sponsor
MIMER Medical College
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Megha Sonawane

Department of Anaesthsia

Study Sites (1)

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