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Treatment of pain in the thoracic gorge with anesthetic injection.

Evaluation of the efficacy of Ropivacaine injection in the anterior and middle scalene muscles guided by ultrasonography in the treatment of Thoracic Outlet Syndrome. - .: .

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
REBEC
Registry ID
RBR-4dx8n4
Enrollment
Unknown
Registered
2019-06-04
Start date
2012-07-30
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Intervention Ultrasonography

Interventions

0.375% ropivacaine injection in the doses of 2.5 ml in each ventricle of the anterior and middle scolenes muscles, guided by ultrasonography,compared to the skin touch with the same syringe-needle set
Drug

Sponsors

Instituto de Medicina Fisica e Reabilitação - IMREA - HCFMUSP
Lead Sponsor
Instituto de Ortopedia e Traumatologia – IOT da Faculdade de Medicina da Universidade de São Paulo.
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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. 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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactChennyfer;CHENNYFER Rached;RACHED

Universidade Nove de Julho;Universidade Nove de Julho

chennyferr@yahoo.com.br;chennyferr@yahoo.com.br1150836781;+55011992992424

Outcome results

None listed

Source: REBEC (via WHO ICTRP)