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Ultrasound Guided Supraclavicular Brachial Plexus Block, Volume Comparison of Local Anaesthetics and Diaphragmatic Motility.

B

B.P. Koirala Institute of Health Sciences

Status and phase

Unknown
Phase 4

Conditions

Sucessful Block With Less Hemidiaphragmatic Paresis in Distal Upper Arm Fracture

Treatments

Procedure: ultra sound guided supraclavicular brachial plexus block

Study type

Interventional

Funder types

Other

Identifiers

NCT03476694
IRC/1091/017

Details and patient eligibility

About

Brachial plexus block as done by landmark technique use large volume of local anaesthetics (at least 30-40 ml), leading to higher incidence of phrenic nerve involvement and diaphragmatic dysfunction. With use of ultrasound dose of local anaesthetic can be reduced. Volume as low as 20 ml when use by ultrasound guidance has shown to provide successful block with no hemidiaphragmatic palsy when compared with nerve stimulation technique. But no study has compared the different volumes of drug on success rate and diaphragmatic motility.So in this study , the investigators want to compare the incidence of hemidiaphragm paralysis and success of block with different volumes of local anaesthetic , so that the lowest effective dose with higher safety profile can be determined.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion

  • Age between 18 and 60 years undergoing distal arm surgery
  • American Society of Anesthesiologists physical status 1 to 3
  • Able to give informed consent
  • Body weight greater than 50 kg

Exclusion

  • Patient refusal for supraclavicular block.
  • Inability to obtain informed consent.
  • Contraindication to Brachial plexus block
  • Pulmonary and cardiac disorders
  • Pregnancy
  • Allergy to local anesthetic
  • Chest or shoulder deformities

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

20ml of 0.75% Ropivacine
Experimental group
Treatment:
Procedure: ultra sound guided supraclavicular brachial plexus block
25ml of 0.75% Ropivacine
Experimental group
Treatment:
Procedure: ultra sound guided supraclavicular brachial plexus block

Trial contacts and locations

1

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Central trial contact

shambhu adhikari, md resident

Data sourced from clinicaltrials.gov

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