Use of Costoclavicular block in Frozen shoulder syndrome to produce analgesia

Costoclavicular block in shoulder adhesive capsulitis- A clinical& Radiocontrast corelation assessing Analgesic efficacy

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/02/040397

Enrollment

Registered

2022-02-17

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: - Health Condition 2: M750- Adhesive capsulitis of shoulder Health Condition 3: M256- Stiffness of joint, not elsewhereclassified

Interventions

Intervention1: Costoclavicular Block in Shoulder Adhesive Capsulitis A Clinical and Radiocontrast Corelation Assessing Analgesic Efficacy : Block Procedures will be performed in a dedicated block r

Eligibility

Inclusion criteria

Inclusion criteria: BMI <25

Exclusion criteria

Exclusion criteria: Patient with MRI noncompatible implant, history of surgery of ipsilateral clavicle/ shoulder, history of MRI contrast/ local anaesthetic drug allergy COPD, PREGNANCY,Contralateral Phrenic nerve paresis, diabetes mellitus

Design outcomes

Primary

Measure	Time frame
- To evaluate analgesic efficacy of costoclavicular block. Adequate analgesia will help patient to perform shoulder rehabilitation exercises efficiently.Timepoint: Post injection patient will be monitored in recovery room for vital signs every 10min for 1hr. Patients SPADI score will be evaluated at 1st hr by shoulder surgery resident. Two hours later SPADI will be reassessed and post block 50% reduc-tion in shoulder pain will be taken as positive response. A clinical score would be assigned to patient. After surgeon finishes clinical assessment, patient will be shifted to scan area for performing ipsilateral shoulder & neck MRI scan.	—

Measure

Time frame

- To evaluate analgesic efficacy of costoclavicular block. Adequate analgesia will help patient to perform shoulder rehabilitation exercises efficiently.Timepoint: Post injection patient will be monitored in recovery room for vital signs every 10min for 1hr. Patients SPADI score will be evaluated at 1st hr by shoulder surgery resident. Two hours later SPADI will be reassessed and post block 50% reduc-tion in shoulder pain will be taken as positive response. A clinical score would be assigned to patient. After surgeon finishes clinical assessment, patient will be shifted to scan area for performing ipsilateral shoulder & neck MRI scan.

—

Secondary

Measure	Time frame
To understand the spread of contrast with help of MRI images after costocla-vicular block - To assess incidence of hemidiaphragmatic paresis. Timepoint: 2hr	—

Countries

India

Contacts

Public ContactAvinash Gaikwad

Sancheti institute of orthopaedics and rehabilitation

avipune22@gmail.com8007778750

Outcome results

None listed

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