To distinguish the safety and potency of clavipectoral fascial plane block with interscalene brachial plexus block in clavicular surgeries along with superficial cervical plexus block

Comparing safety and efficacy of ultrasound guided clavipectoral fascial plane block with interscalene brachial plexus block in clavicular surgeries along with superficial cervical plexus block - a randomized study. - NOT APPLICABLE

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/08/056701

Enrollment

Registered

2023-08-21

Start date

Unknown

Completion date

Unknown

Last updated

2023-09-18

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

Control Intervention1: CLAVIPECTORAL FASCIAL PLANE BLOCK: The baseline of diaphragm movement is measured in group 1 and diaphragm movement will be measured after 30 min of block. The incidence of he

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient aged between 18 to 60 years of age. 2. Patient of either gender. 3. ASA-PS 1 or ASA-PS II . 4. Patient will be posted for elective internal fixation of clavicle fracture

Exclusion criteria

Exclusion criteria: 1. Patient who refuse to participate. 2. Patient belonging to ASA-PS III and above. 3. Patient with respiratory insufficiency (bilateral rib fractures, obstructive emphysema). 4. Patient with abnormal blood coagulation. 5. Patient with puncture site infection. 6. Patients who cannot lie down / non-co-operative / psychiatric illness.

Design outcomes

Primary

Measure	Time frame
Determine the probability of hemi-diaphragmatic paresis in both groups measured by calculating hemi-diaphragmatic excursion during sigh test.Timepoint: The range of diaphragmatic movement from the expiratory position to deep inspiration (sigh test) was recorded before & 30 min after the block.	—

Secondary

Measure	Time frame
To compare onset of sensory block by using cold swab test in both groupsTimepoint: 1-10 mins;compare the intraoperative hemodynamic effect in both groups.Timepoint: intraoperative-10 min before block & 5,10,20,30,45,60,75,90,105,120150,180 ;compare the duration of post op analgesia using visual analogue study (VAS) in both groups.Timepoint: 2,4,6,8 hours	—

Countries

India

Contacts

Public ContactPRASANTH D

SRI MANAKULAVINAYAGAR MEDICAL COLLEGE AND RESEARCH INSTITUTE

drpathin2@gmail.com9787740890

Outcome results

None listed

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