Comparison of efficiency of two different doses of magnesium sulphate when added to local anesthetic in supraclavicular block( which are given in upper limb surgeries) in reducing post operative pain

Phase 3

Not yet recruiting

• Registration Number: CTRI/2021/07/034681
• Lead Sponsor: Bharati hospital and research centre Pune

Brief Summary

This is a randomised controlled double blinded prospective study to compare the efficacy of two different doses of magnesium sulphate 150 mg and 250 mg when added to local anesthetics in USG Guided  supraclavicular block in elective upper limb surgeries .Total 90 patients aged between 18 to 60 years will be divided into two groups , Group M1- 12 ml  0.5% Bupivacaine plus  12 ml 2% lignocaine with adrenaline plus magnesium sulphate 150 mg( 0.3ml), Group M2- 12 ML 0.5% Bupivacaine plus 12 ml 2% lignocaine with adrenaline plus magnesium sulphate 250 mg(0.5 ml) and we compare the following parameters- Onset and duration of sensory block, Onset  and duration of motor block, Duration of post operative analgesia, total analgesic requirement in 24 hours & monitor for side effects if any.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-07-07
• Study Start: 2021-07-27

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

PATIENT AGED BETWEEN 18 TO 60 YEARTS OF AGE BOTH SEXES ASA GRADE I AND II POSTED FOR ELECTIVE UPPER LIMB SURGERY UNDER SUPRACLAVICULAR BLOCK.

Exclusion Criteria

PATIENT REFUSAL TO PARTICIPATE IN STUDY PATIENT ALLERGIC TO LOCAL ANAESTHETIC AGENTS PATIENT ON CHRONIC TREATMENT WITH CALCIUM CHANNEL BLOCKERS PATIENT WITH HEART BLOCK PATIENT ON ANTICOAGULANTS PATIENT WITH PRE EXISTING NEUROPATHY.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
DURATION OF POST OPERATIVE ANALGESIA	ONSET AND DURATION OF MOTOR AND SENSORY BLOCK

Secondary Outcome Measures

Name	Time	Method
TOTAL ANALGESIC REQUIREMENT	POST OPERATIVELY FOR TWENTY FOUR HOURS

Trial Locations

Locations (1)

BHARATI HOSPITAL AND RESEARCH CENTRE; 🇮🇳 Pune, MAHARASHTRA, India

BHARATI HOSPITAL AND RESEARCH CENTRE

🇮🇳Pune, MAHARASHTRA, India

DR SUHAIL ASHRAF

Principal investigator

7907154962

drsuhailashraf94@gmail.com