A study to compare two types of nerve blocks in collar bone surgeries

A randomised comparative study to assess the efficacy of Interscalene brachial plexus block with superficial cervical plexus block versus Clavipectoral fascial plane block with superficial cervical plexus block in clavicle surgeries under ultrasound guidance. - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/12/099097

Enrollment

Registered

2025-12-15

Start date

Unknown

Completion date

Unknown

Last updated

2026-01-12

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: a: b Intervention2: Clavipectoral fascial plane block with Superficial cervical plexus block: A single injection of 22ml of 0.5% Levobupivacaine, 2% Lignoadrenaline and 8mg of Dexametha

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status 1 and 2 BMI less than 30

Exclusion criteria

Exclusion criteria: Patients unwilling to enroll for study. Known allergy to local anaesthetics. Infection at the site of block placement. Severe cardio-cerebrovascular diseases. Respiratory insufficiency. Bleeding disorders. Chronic opioids usage.

Design outcomes

Primary

Measure	Time frame
To compare the analgesic efficacy of ultrasound guided Clavipectoral fascial plane block with Superficial cervical plexus block versus ultrasound guided Interscalene brachial plexus block with Superficial cervical plexus block in patients undergoing clavicle fracture surgeries measured using Visual Analogue Scale.Timepoint: Postoperatively at 1,2,4,6,8,10, 12,16,20 and 24 hours.	—

Secondary

Measure	Time frame
To determine the ease of technique by means of block performance time.Timepoint: From needle insertion till the needle is taken out after final injection;To assess incidence of complications.Timepoint: From needle insertion till 24 hours postoperatively ;To evaluate patient satisfaction score using five-point Likert scaleTimepoint: End of surgery till 24 hours postoperatively	—

Countries

India

Contacts

Public ContactSridevi P

Aarupadai Veedu Medical College and Hospital, Pondicherry

dr.sripanneer30@gmail.com8072586724

Outcome results

None listed

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