comparison of effects of two different blocks in collar bone surgery

A comparison of ultrasound-guided superficial cervical plexus block combined with clavipectoral fascial plane block and blockade of supraclavicular nerves along with upper trunk of brachial plexus The SCUT block in clavicle surgery a single-centre, double-blind, randomized controlled trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/068199

Enrollment

Registered

2024-05-31

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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: Clavicle surgery: Group II patients receiving supraclavicular nerves along with upper trunk of brachial plexus SCUT Block Patients will be placed in a semi-lateral position, with the af

Eligibility

Inclusion criteria

Inclusion criteria: Patients classified as American Society of Anesthesiologists (ASA) I-II Patients with unilateral clavicular fractures undergoing elective internal fixation

Exclusion criteria

Exclusion criteria: Exclusion criteria included cardio-cerebrovascular diseases, respiratory insufficiency, abnormal blood coagulation, puncture site infection, continuous use of analgesics for the past three months, and allergy to local anesthetics.

Design outcomes

Primary

Measure	Time frame
The effectiveness of the block will be assessed in the sternoclavicular joint, midclavicular region, and acromioclavicular joint. Four levels will be established: zero indicated no decreased sensation, one indicated decreased sensitivity to puncture, two indicated no sensitivity to puncture, and three indicated no tactile sensitivity. Correct blocks are defined as achieving levels two or three.Timepoint: The effectiveness of the block will be assessed at 30 minutes in three areas: the sternoclavicular joint, midclavicular region, and acromioclavicular joint.	—

Measure

Time frame

The effectiveness of the block will be assessed in the sternoclavicular joint, midclavicular region, and acromioclavicular joint. Four levels will be established: zero indicated no decreased sensation, one indicated decreased sensitivity to puncture, two indicated no sensitivity to puncture, and three indicated no tactile sensitivity. Correct blocks are defined as achieving levels two or three.Timepoint: The effectiveness of the block will be assessed at 30 minutes in three areas: the sternoclavicular joint, midclavicular region, and acromioclavicular joint.

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Secondary

Measure	Time frame
The secondary outcome of interest is the time to first use of analgesics.Timepoint: Visual Analog Scale (VAS) scores will be recorded at 6, 12, and 24 hours after surgery	—

Countries

India

Contacts

Public ContactDr Savita Gupta

Government Institute Of Medical Sciences

dr.gsavita@gmail.com8750657382

Outcome results

None listed

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