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A study to find out which works better for intraoperative and postoperative pain relief in clavicle fracture surgery using superficial cervical plexus block combined with interscalene block vs clavipectoral block under ultrasound guidance .

Ultrasound guided superficial cervical plexus block with interscalene block vs clavipectoral block in clavicle surgery - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096793
Enrollment
60
Registered
2025-11-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: M849- Disorder of continuity of bone, unspecified

Interventions

Intervention1: Superficial cervical plexus block with clavipectoral block: The superficial cervical plexus block combined with clavipectoral block given under ultrasound guidance Intervention2: Superf

Sponsors

Dr Sasirekha S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient willing to participate and who give informed consent 2.American Society Of Anaesthesiology class I & II 3.Patient planned for clavicle surgery

Exclusion criteria

Exclusion criteria: American Society Of Anaesthesiology class III and more Pregnant and lactating mother Patient preexisting with pulmonary and neurological disorders Bleeding disorders Local site infection Allergy to local anaesthetic agent

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of the block in terms of onset and duration of sensory blockade, Onset and duration of motor blockade and watch for any complicationsTimepoint: The sensory and motor blockade will be assessed intraoperatively and postoperatively for 24 hours

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Madhan

Indira Gandhi Government General Hospital and Postgraduate Institute

drmadhan76@gmail.com7373933999

Outcome results

None listed

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