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Comparative study of two USG guided continuous Infraclavicular brachial plexus block for pain management in upper limb orthpaedic surgeries

Comparison of continuous lateral sagittal and costoclavicular infraclavicular brachial plexus block for postoperative analgesia in patients undergoing upper limb orthopaedic procedures: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030766
Enrollment
80
Registered
2021-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: S529- Unspecified fracture of forearm

Interventions

Intervention1: Group 1 - Costoclavicular block in upper limb orthopaedic surgery : Group 1 - Costoclavicular block with continous catheter technique in upper limb orthopaedic surgery Drug Volume- 20 m

Sponsors

Department of Anaesthesiology AIIMS Patna
Lead Sponsor
Department of Anaesthesiology AIIMS Patna
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: All healthy patients of ASA PS 1 & 2 with age group 18-65 years (Either sex) and BMI < 30kg/m2 who are scheduled for upper extremity orthopedic surgery at or distal to the elbow, are in inclusion criteria.

Exclusion criteria

Exclusion criteria: Exclusion criteria - 1)ASA physical status > Grade III 2)Age 65 years 3)BMI > 30 kg/m2 4)Patientâ??s refusal 5)Allergic to local anaesthetics 6)Local infection at or near the needle insertion site 7)Coagulopathy or medical anticoagulation 8)Traumatic nerve injury in the upper extremity or neck 9)Preexisting neuro deficits in the distribution of the block 10)Previous surgery or condition in the neck that may distort brachial plexus anatomy

Design outcomes

Primary

MeasureTime frame
To compare the requirement of post-operative analgesics (total dose of local anaesthetics) in 24 hours postoperativelyTimepoint: 1 year—

Secondary

MeasureTime frame
To evaluate - 1) Time of rescue analgesia 2) Average 24-hour NRS score post operatively 3) Time required inserting catheter 4) Discomfort score during catheter insertion 5) Time to develop sensory and motor blockade, 6) Worst NRS score 7) Satisfaction scores Timepoint: 1 year—

Countries

India

Contacts

Public ContactSoumyajit Mondal

All India Institute of Medical Sciences, Patna

chandni.doc@gmail.com9062606661

Outcome results

None listed

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