Treatment of pain in the thoracic gorge with anesthetic injection.

Phase 4

• Conditions: Intervention Ultrasonography; E01.370.350.850.855

• Registration Number: RBR-4dx8n4
• Lead Sponsor: Instituto de Medicina Fisica e Reabilitação - IMREA - HCFMUSP

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-06-04
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

this study were subjects with a diagnosis of nonspecific, Thoracic Outlet Syndrome who included criteria for inclusion with pain in upper limbs and / or neck pain without radiculopathy or neurological impairment of the limb in question due to compressive or encephalic root causes.

Exclusion Criteria

Clinical instability with acute medical conditions.
Hypersensitivity to administered medication.
Injury of the rotator cuff previously diagnosed by some imaging examination and justifying pain.
Fibromyalgia previously diagnosed.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
CHARACTERISTICS OF THE ARM, SHOULDER AND HAND presentation of the method used to verify the expected result: DASH scale - DISABILITIES OF THE ARM, SHOULDER, AND HAND; presentation of the parameters: percentage, average along the scale, used for the actual final result.<br><br>Improvement of the functionality in 1 year, verified through the DASH chart, from the observation of a variation of at least 5% in the pre- and post-intervention evaluations.

Secondary Outcome Measures

Name	Time	Method
<br>Pain improvement at 1 year, verified through the Visual Analogue Scale (EVA) scale. a) Assuming a variation of at least 5% in pre and post-intervention measurements.