FindTrial
Sign In

Effect of combining superficial cervical plexus block with clavipectoral fascial plane block or interscalene brachial plexus block using ultrasound machine with local anesthesia 0.375% ropivacaine for collar bone fracture surgeries

A Prospective Randomized Controlled Comparative Study of Combining Ultrasound Guided Superficial Cervical Plexus Block with Clavipectoral Fascial plane Block and Interscalene Brachial Plexus Block using 0.375% Ropivacaine for Elective Clavicle Surgeries. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065862
Enrollment
100
Registered
2024-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: S420- Fracture of clavicle

Interventions

Intervention1: Superficial cervical plexus block with Interscalene brachial plexus block: Superficial cervical plexus block with 7ml of 0.375% Ropivacaine Interscalene brachial plexus block with 20 m

Sponsors

K MUNI SRUTHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients belonging to American Society of Anaesthesiologists Physical Status I and II. 2. Patients undergoing elective surgery for clavicle fractures.

Exclusion criteria

Exclusion criteria: 1. Patients refusing for the procedure. 2. Patients with history of allergy, sensitivity or any kind of reactions to local anesthetic agents. 3. Patients with coagulation abnormalities. 4. Patients with cardiovascular and cerebrovascular diseases. 5. Patients with infection at the injection site. 6. Patients with history of Chronic Obstructive Pulmonary Disease and Pleural effusion.

Design outcomes

Primary

MeasureTime frame
The time at which the first use of rescue analgesic drug. This will be assessed in the postoperative period after the surgery.Timepoint: Pain will be assessed using Pain Score : Visual Analogue Scale at 6th , 12th and 24th hour postoperatively—

Secondary

MeasureTime frame
Diaphragm excursion measurement will be done during normal tidal volume breaths & deep breaths before giving block preoperatively & also intraoperatively & also postoperativelyTimepoint: Diaphragm excursion measurement will be assessed using Ultrasound in centimeters just before giving block as preblock value & at 30th minute after giving block & also at 4th hour after giving block;The motor effect of all the blocks will be assessed preoperatively after giving block at shoulder joint, elbow joint, wrist joint, metacarpophalangeal & interphalangeal joints of fingersTimepoint: The motor effect will be assessed immediately after giving block & also at 30th minute after giving block to check for the onset time.;The sensory effect of all the blocks will be assessed in three areas: sternoclavicular joint, mid clavicle, acromioclavicular joint preoperatively after giving block.Timepoint: The sensation will be assessed immediately after giving block & also at 30th minute after giving block to check for the onset time.—

Countries

India

Contacts

Public ContactGowni Geetha

Navodaya Medical College, Hospital and Research Centre

kumargowtham1994@gmail.com9353116870

Outcome results

None listed

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