A CLINICAL TRAIL TO STUDY COMPARISON BETWEEN ROPIVACAINE WITH OR WITHOUT MAGNESIUM SULPHATE FOR POST OPERATIVE PAIN RELIEF IN LOWER ABDOMINAL SURGERY BY USING TRANSVERSUS ABDOMINIS PLANE BLOCK

Phase 3

Not yet recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2022/02/040012
• Lead Sponsor: Dr Abhinetri Danashetti

Brief Summary

This Study Is a Prospective Interventional Study, With Duration Of 18Months



And Sample Size Of 60 Patients divided into two groups

GroupA and Group B with 30 patients each



Sampling procedure:Simple Random sampling

GroupA-30case Inj .Ropivocaine 0.25% 20ml with 2.5ml of

Normal saline GroupB-30cases Inj Ropivocaine 0.25% 20ml

With 2.5ml of Magnesium Sulphate(500mg) conducted in our

Institution and Research Hospital. Primary outcome will be to provide

Post operative analgesia after lower abdominal surgeries using TAP Block

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2022-02-02
• Study Start: 2022-04-02

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• 1.All patients posted for lower abdominal surgery.
• 2.Age group 18-60 years.
• 3.Patients of American Society of Anaesthesiology grade 1 and II.

Exclusion Criteria

• Patients on any opioid or any sedative medication in the week prior to the surgery.
• Patients with history of alcohol or drug abuse.
• Patients who have known allergies to any of test drugs.
• Patients with coagulation disorders or on anti coagulant drugs.
• Patients with cardiac disease (heart block, premature ventricular contractions, significant bradyarrhythmias, left ventricular failure.) 6.
• Patients with respiratory diseases.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To study the efficacy of Ropivacaine with or without Magnesium sulphate for postoperative analgesia.	From Time of Injection to First 6-8 Hours After The Surgery

Secondary Outcome Measures

Name	Time	Method
To Study Systemic Side Effects.	From Time Of Injection To 6hr, 12hr, 24hr After The Surgery

Trial Locations

Locations (1)

Basaveshwar Teaching and General Hospital; 🇮🇳 Gulbarga, KARNATAKA, India

Basaveshwar Teaching and General Hospital

🇮🇳Gulbarga, KARNATAKA, India

Dr Abhinetri Danashetti

Principal investigator

9481983493

abhinetridanashetti1994@gmail.com