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A Randomized Study Comparing Hemi-diaphragmatic Paresis In Costoclavicular And Supraclavicular Nerve Block For Forearm Surgery

Hemi-diaphragmatic Paresis Following Costoclavicular Versus Supraclavicular Brachial Plexus Block in Forearm Surgeries: A Prospective Randomized Controlled Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/113144
Enrollment
60
Registered
2026-06-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: S50-S59- Injuries to the elbow and forearm

Interventions

Intervention1: Hemi-diaphragmatic Paresis Following Costoclavicular Versus Supraclavicular Brachial Plexus Block: gg Intervention2: Ultrasound-Guided Costoclavicular Brachial Plexus Block (CCB): Pati

Sponsors

GMERS Medical College and Hospital Gotri, Vadodara
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Age 18 to 60 years -Weight: 40 to 80 kg -American society of anaesthesiology Grade: I, II

Exclusion criteria

Exclusion criteria: -Patient s refusal to take part in study -Polytrauma -Bleeding disorders -Allergy to local anaesthetics -Local site infection -Pre-existing neuropathy on surgical limb -Neuromuscular disease -Significant pulmonary disease

Design outcomes

Primary

MeasureTime frame
Comparison of incidence of hemi diaphragmatic paresis (diaphragm excursion- DE and diaphragm thickness fraction - DTF) between USG guided costoclavicular (CCB) vs supraclavicular (SCB) block in patients undergoing forearm surgery.Timepoint: Pre-operatively three measurements of diaphragm excursion and thickness fraction will be recorded and similar recordings made two hour post-operatively in recovery room. Average of all readings will be considered.

Secondary

MeasureTime frame
Comparison of PEFR (peak expiratory flow rate)Timepoint: Pre-operatively and two hour post-operatively three readings of PEFR will be measured and highest value will be considered.;Any complication (respiratory distress, pneumothorax, hematoma, LA toxicity, allergy, neuronal injury, etc.)Timepoint: Any complications occuring 24 hrs after block.

Countries

India

Contacts

Public ContactDabgar Keval Ashokkumar

GMERS Medical College and Hospital, Gotri, Vadodara

dr.dharatushar@gmail.com9979877486

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026