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Clinical Trials/CTRI/2023/12/060726
CTRI/2023/12/060726
Not yet recruiting
未知

A COMPARATIVE STUDY OF EFFICACY OF TWO DIFFERENT STRENGTH OF BUPRENORPHINE AS A SPINAL ADJUVANT TO ROPIVACAINE IN PATIENTS UNDERGOING OPEN INGUINAL HERNIA SURGERIES; A RANDOMISED DOUBLE BLIND CONTROLLED TRIAL. - nil

MGIMS0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: K400- Bilateral inguinal hernia, with obstruction, without gangrene

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: K400- Bilateral inguinal hernia, with obstruction, without gangrene
Sponsor
MGIMS
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
MGIMS

Eligibility Criteria

Inclusion Criteria

  • •?American Society of Anesthesiologists Grade I and II patients.
  • •?Age above 18 years of any gender
  • •?Patients undergoing open Inguinal hernia Surgeries.
  • •?Height is more than 4 feet.

Exclusion Criteria

  • •?American Society of Anesthesiologists Grade III and IV patients.
  • •?Patients with known contraindications for spinal anaesthesia: bleeding disorders, local infection.
  • •?Patients with hemodynamic instability.
  • •?Patient with allergy to or history of hypersensitivity to local anaesthetic.
  • •?Emergency surgeries.
  • •?Patient’s refusal.

Outcomes

Primary Outcomes

Not specified

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