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Study on how adding an additional medicine magnesium sulphate affects the effectiveness and pain relief of local anaesthesia for hand surgeries.

Effect of 2 percent Xylocaine with adrenaline and 0.5 percent Bupivacaine in supraclavicular brachial plexus block with or without magnesium sulphate as an adjuvant - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/105013
Enrollment
70
Registered
2026-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: Group C (control group) is Local anaesthetics- Bupivacaine and Xylocaine with adrenaline: 15 ml of 0.5 percent bupivacaine added to 12.5 ml of 2 percent Xylocaine with adrenaline added

Sponsors

Parul Institute of Medical Sciences and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to sign informed written Consent, belonging to American Society of Anesthesiology (ASA) Grade I/II and those posted for elective upper limb surgeries below midarm.

Exclusion criteria

Exclusion criteria: Allergy to local anaesthetic agents Infection at the puncture site Severe obstructive/Restrictive lung disease Preoperative sensory or motor deficits of upper limbs. Patient with traumatic or pre- existing nerve injury in the limb to be operated on and clavicular fracture in the operative limb. Patient with bilateral Upper limb fractures Patient with psychiatric disorders Pregnant and lactating female Emergency surgery Morbid obesity Patients with Coagulopathy Patients under ASA Grade III and IV

Design outcomes

Primary

MeasureTime frame
Effect of mgso4 added to local anaesthetics in supraclavicular brachial plexus block characteristics, quality and duration postoperative analgesia.Timepoint: From 0 minute(time when block given) to 12 hrs after block

Secondary

MeasureTime frame
The present study will be undertaken to compare two study groups with the following objectives Onset as well as duration of the sensory block Onset as well as duration of the motor block Duration as well as quality of AnalgesiaTimepoint: From 0 minutes (block given time) to 12 hours post operative period

Countries

India

Contacts

Public ContactDr Sudha Shah

Parul University, Parul Institute of Medical Sciences and Research

sudha1707@yahoo.co.in9978532450

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026