A study to compare the efficacy of two different volumes of injection Ropivacaine in brachial plexus block in upper limb surgeries

Phase 4

Not yet recruiting

• Conditions: Fracture of upper end of ulna, (2) ICD-10 Condition: S521||Fracture of upper end of radius, (3) ICD-10 Condition: S522||Fracture of shaft of ulna, (4) ICD-10 Condition: S523||Fracture of shaft of radius, (5) ICD-10 Condition: S525||Fracture of lower end of radius, (6) ICD-10 Condition: S526||Fracture of lower end of ulna, (7) ICD-10 Condition: S62||Fracture at wrist and hand level, (8) ICD-10 Condition: S568||Injury of other muscles, fascia and tendons at forearm level,

• Registration Number: CTRI/2023/07/055520
• Lead Sponsor: Pacific Medical College And Hospital

Brief Summary

Study to compare time of onset, efficacy and duration of motor and sensory block with two different volumes (30ml and 20ml) of Injection Ropivacaine 0.5% when given as ultrasound guided supra clavicular brachial plexus block in upper limb surgeries so that we can use low volume of local anaesthetic agent to achieve desired effect of anaesthesia.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-07-22
• Last Update Posted: 2023-11-07

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

Adult patients aged between 18-60 years American Society of Anesthesiologists Physical Status I and II Scheduled for elective upper limb surgeries under Supraclavicular block Body weight between 50-80 kgs.

Exclusion Criteria

Lack of patient consent ASA grade III, IV, V Patients with anticipated difficult intubation- Mallampati Grade 3 and 4 Any other Co-morbidities (COPD, Ischemic Heart Disease, Hypertension, Diabetes Mellitus, Renal & hepatic Dysfunction, etc.) Allergic to local anesthetics Coagulation disorder Pregnancy Body weight less than 50 kgs and more than 80 kgs Emergency surgeries.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of Motor block & Sensory block	24months
Time taken for first analgesic dose	24months
Time of onset of Motor block & Sensory block	24months

Secondary Outcome Measures

Name	Time	Method
Any side effects	Haemodynamic stability

Trial Locations

Locations (1)

Pacific Medical College And Hospital; 🇮🇳 Udaipur, RAJASTHAN, India

Pacific Medical College And Hospital

🇮🇳Udaipur, RAJASTHAN, India

Dr Prakash Chandra Audichya

Principal investigator

9929721889

prakash.audichya10@gmail.com