Effective volume of local anaesthetic,Ultrasound-Guided Infraclavicular Brachial Plexus Block

Effective volume of local anaesthetic for ultrasound guided infraclavicular brachial plexus block- A Prospective randomised control trail. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075311

Enrollment

Registered

2024-10-15

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided infraclavicular brachial plexus block: Group A will be receiving Infraclavicular brachial plexus block with 25ml of local anaesthetic- ropivacaine 0.5% and Group B wil

Eligibility

Inclusion criteria

Inclusion criteria: -Patients who have given valid written consent -Patients above 18 years of age with American society of Anesthesiologists (ASA) physical status 1-3 posted for ORIF upper limb for fractures below mid humerus

Exclusion criteria

Exclusion criteria: -Patient refusal -Coagulopathy-Decreased platelet count, increased PT, aPTT and INR -Allergy or hypersensitivity to local anesthetics -Active infection at the site of block ,where needle is inserted -Uncooperative or noncompliant patients -Neurological or neuromuscular disorders involving upper extremities

Design outcomes

Primary

Measure	Time frame
To compare efficacy of 25ml of 0.5%ropivacaine with 30ml of 0.5%ropivacaine on action anaesthesia following ultrasound-guided infraclavicular brachial plexus block Timepoint: Patients will be divided into two groups using computer generated random number table Group A-Receiving Infraclavicular brachial plexus block with 25ml of local anaesthetic Ropivacaine 0.5% Group B-Receiving Infraclavicular brachial plexus block with 30ml of local anaesthetic Ropivacaine 0.5% The sensory and motor block establishment in different territories at 0th min,5th min,10th min,15th min,20th min,25th min,30th min.	—

Measure

Time frame

To compare efficacy of 25ml of 0.5%ropivacaine with 30ml of 0.5%ropivacaine on action anaesthesia following ultrasound-guided infraclavicular brachial plexus block Timepoint: Patients will be divided into two groups using computer generated random number table Group A-Receiving Infraclavicular brachial plexus block with 25ml of local anaesthetic Ropivacaine 0.5% Group B-Receiving Infraclavicular brachial plexus block with 30ml of local anaesthetic Ropivacaine 0.5% The sensory and motor block establishment in different territories at 0th min,5th min,10th min,15th min,20th min,25th min,30th min.

—

Secondary

Measure	Time frame
To compare onset & duration of postoperative operative analgesia using 25ml & 30ml of 0.5% ropivacaine following ultrasound-guided infraclavicular brachial plexus blockTimepoint: onset of action of drug- at baseline or 0th min, till the time patient complains of pain in postoperative period eg- 6 hours or 8 hours. this is assed by VAS score.	—

Countries

India

Contacts

Public ContactDr Suresh Kumar N

Sri Devaraj URS Medical College Kolar

drskumar6@gmail.com9008222550

Outcome results

None listed

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