A Prospective Randomised Comparative Study for Analgesic and Anaesthetic effects of Two Different Volumes of same concentration of Ropivacaine in Ultrasound Guided Supraclavicular Brachial Plexus Block for Upper Limb Surgeries.

A Prospective Randomised Comparative Study for Analgesic and Anaesthetic effects of Two Different Volumes of 0.75% Ropivacaine in Ultrasound Guided Supraclavicular Brachial Plexus Block for Upper Limb Surgeries in Department of Anaesthesia at SMS Medical College and Attached Group of Hospitals, Jaipur. - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087207

Enrollment

Registered

2025-05-20

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: T07- Unspecified multiple injuries

Interventions

Intervention1: Ultrasound Guided Supraclavicular Brachial Plexus Block for upper limb surgeries: With the help of USG guidance, lesser volume of the drug can be used for supraclavicular block for uppe

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing upper limb surgery. Adult patients weighing 50 to 80 kgs. Patients belonging to ASA class I and II. Patients giving consent for participation.

Exclusion criteria

Exclusion criteria: Patients should not be a part of any other study. History of allergic reaction to local anaesthetics. Patients on anticoagulant therapy and/or history of coagulation disorders. Local infection at the proposed site of supraclavicular brachial plexus block. Patients with psychiatric illness, anxious or agitated. Patients with respiratory illness/compromise. Non cooperative patient. Patients with peripheral sensorineural deficit, suspected compartment syndrome in upper limbs.

Design outcomes

Primary

Measure	Time frame
1. Mean onset and duration of sensory blockade. 2. Mean maximum grade of sensory blockade. 3. Mean onset and duration of motor blockade. 4. Mean maximum grade of motor blockade by Modified Bromage Scale.. 5. Mean duration of analgesia by Numerical Rating Scale. 6. Mean time to first rescue analgesia postoperatively. Timepoint: 1. Mean onset and duration of sensory blockade in minutes at baseline. 2. Mean onset and duration of motor blockade in minutes at baseline. 3. Mean duration of analgesia in minutes by Numerical Rating Scale at baseline, 3 hours, 6 hours, 9 hours, 12 hours, 24 hours postoperatively. 4. Mean time to first rescue analgesia in minutes at baseline, 3 hours, 6 hours, 9 hours, 12 hours, 24 hours postoperatively.	—

Measure

Time frame

1. Mean onset and duration of sensory blockade. 2. Mean maximum grade of sensory blockade. 3. Mean onset and duration of motor blockade. 4. Mean maximum grade of motor blockade by Modified Bromage Scale.. 5. Mean duration of analgesia by Numerical Rating Scale. 6. Mean time to first rescue analgesia postoperatively. Timepoint: 1. Mean onset and duration of sensory blockade in minutes at baseline. 2. Mean onset and duration of motor blockade in minutes at baseline. 3. Mean duration of analgesia in minutes by Numerical Rating Scale at baseline, 3 hours, 6 hours, 9 hours, 12 hours, 24 hours postoperatively. 4. Mean time to first rescue analgesia in minutes at baseline, 3 hours, 6 hours, 9 hours, 12 hours, 24 hours postoperatively.

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Secondary

Measure	Time frame
1. Mean Hemodynamic parameters (HR, SBP, DBP, MAP and Spo2). 2. Proportion of cases which require supplementation of block. 3. Proportion of percentage change in diaphragm movement by USG. 4. Proportion of cases with side effects/complications.Timepoint: 1. Mean Hemodynamic parameters (HR, SBP, DBP, MAP and Spo2) at 0,5,10,15,20,20,25,30,35,40,45,50,55,60 minutes. 2. Percentage change in diaphragm movement by USG at 0, 30 and 60 minutes.	—

Measure

Time frame

1. Mean Hemodynamic parameters (HR, SBP, DBP, MAP and Spo2). 2. Proportion of cases which require supplementation of block. 3. Proportion of percentage change in diaphragm movement by USG. 4. Proportion of cases with side effects/complications.Timepoint: 1. Mean Hemodynamic parameters (HR, SBP, DBP, MAP and Spo2) at 0,5,10,15,20,20,25,30,35,40,45,50,55,60 minutes. 2. Percentage change in diaphragm movement by USG at 0, 30 and 60 minutes.

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Countries

India

Contacts

Public ContactDr Kumud Jangra

Sawai Man Singh Medical College, Jaipur

vandanamangal25@gmail.com9829056816

Outcome results

None listed

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