Teres Major Muscle and Subacromial Impingement Syndrome

NCT ID: NCT02374125

Last Updated: 2015-02-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-11-30

Study Completion Date

2015-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

There is not a clear understanding of the origin of symptoms perceived by patients with impingement of the soft tissue structures of the subacromial space. Tendinopathy, tendon rupture or other pathologies, are present in asymptomatic subjects and subjects with symptoms and structural integrity can also be found.

Patients diagnosed with subacromial impingement syndrome frequently have myofascial trigger points in the teres major muscle. Travell and Simons reported that the symptoms caused by trigger points in this muscle are similar to those experienced by patients diagnosed with impingement syndrome, but a literature search provides few results regarding relationship between subacromial impingement syndrome and presence of myofascial trigger points in the teres major muscle.

This study aims to provide evidence of the results that can be obtained with a specific approach of teres mayor muscle by two manual techniques, Trigger Point Pressure Release and Diacutaneous Fibrolysis, in subjects with subacromial impingement syndrome, a condition that still representing both a diagnostic and therapeutic challenge. Secondary objective is to compare the outcomes between both techniques to select for each patient the most appropriate to their needs and characteristics.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Trigger Points in Teres Major Muscle Subacromial Impingement Syndrome

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Fibrolysis Group

Actual Diacutaneous Fibrolysis and protocolized physiotherapy

Group Type EXPERIMENTAL

Diacutaneous Fibrolysis

Intervention Type DEVICE

Applied only around teres major muscle.

Protocolized physiotherapy

Intervention Type OTHER

Exercises, TENS and cryotherapy

Pressure Group

Trigger Point Pressure Release and protocolized physiotherapy

Group Type EXPERIMENTAL

Trigger Point Pressure Release

Intervention Type OTHER

Applied only in teres major muscle trigger points.

Protocolized physiotherapy

Intervention Type OTHER

Exercises, TENS and cryotherapy

Control Group

Protocolized physiotherapy

Group Type ACTIVE_COMPARATOR

Protocolized physiotherapy

Intervention Type OTHER

Exercises, TENS and cryotherapy

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Diacutaneous Fibrolysis

Applied only around teres major muscle.

Intervention Type DEVICE

Trigger Point Pressure Release

Applied only in teres major muscle trigger points.

Intervention Type OTHER

Protocolized physiotherapy

Exercises, TENS and cryotherapy

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age 18 years and over
* Clinical diagnosis of Subacromial Impingement Syndrome.
* Detectable trigger points in teres major muscle.
* Sign informed consent form.

Exclusion Criteria

* Diacutaneous Fibrolysis contraindications
* Previous shoulder surgery (\<1year)
* Language barriers or cognitive issues that limit their ability to provide informed consent and participate in research.
* Patients with a pending litigation or court claim.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Martín Barra

Role: PRINCIPAL_INVESTIGATOR

IDIAP JORDI GOL

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Catalan Health Institut. Sant Ildefons Rehabilitation Service

Cornellà de Llobregat, Barcelona, Spain

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Spain

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Martin Barra

Role: CONTACT

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Martín Barra

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

P14/033

Identifier Type: -

Identifier Source: org_study_id