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A RANDOMISED DOUBLE BLIND CONTROL STUDY TO COMPARE THE EFFICACY OF TWO DIFFERENT STRENGTH OF BUPRENOPHINE AS A SPINAL ADJUVANT WITH 0.75% ROPIVACAINE IN ADULT PATIENT UNDERGOING OPEN INGUINAL HERNIA SURGERIES.

Not yet recruiting
Conditions
Bilateral inguinal hernia, with obstruction, without gangrene,
Registration Number
CTRI/2023/12/060726
Lead Sponsor
MGIMS
Brief Summary

TO COMPARE TWO DIFFERENT STRENGTHS OF BUPRINORPHINE ON POSTOPERATIVE ANALGESIA,INTRAOP HEMODYNAMIC CHANGES,TIME FOR SENSORY AND MOTOR BLOCK

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
104
Inclusion Criteria
  • â—American Society of Anesthesiologists Grade I and II patients.
  • â—Age above 18 years of any gender â—Patients undergoing open Inguinal hernia Surgeries.
  • â—Height is more than 4 feet.
Exclusion Criteria
  • â—American Society of Anesthesiologists Grade III and IV patients.
  • â—Patients with known contraindications for spinal anaesthesia: bleeding disorders, local infection.
  • â—Patients with hemodynamic instability.
  • â—Patient with allergy to or history of hypersensitivity to local anaesthetic.
  • â—Emergency surgeries.
  • â—Patient’s refusal.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
POSTOPERATIVE ANALGESIA15MINS,1 HR,3HRS
Secondary Outcome Measures
NameTimeMethod
INTRAOP HEMODYNAMIC PARAMETRES AND TIME FOR SENSORY AND MOTOR BLOCK5MINS,15MINS,30 MINS,45 MINS

Trial Locations

Locations (1)

MGIMS,KASTURBA HOSPITAL.

🇮🇳

Wardha, MAHARASHTRA, India

MGIMS,KASTURBA HOSPITAL.
🇮🇳Wardha, MAHARASHTRA, India
TANU CHOUDHARY
Principal investigator
6375427821
tanuchoudhary@mgims.ac.in

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