Effectiveness of ECA Cream on Calcifying Shoulder Tendinitis
NCT ID: NCT02986035
Last Updated: 2017-01-31
Study Results
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.
COMPLETED
NA
10 participants
INTERVENTIONAL
2016-10-31
2016-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
1. Reduction or removal of shoulder calcifications
2. Functional improvements
3. Pain improvements 10 subjects will be assessed prior and 1 and 2 months post intervention onset. The intervention will consist in the application of the ECA cream in the affected shoulder twice a day during 1 month.
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention
ECA cream
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
ECA cream
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* diagnosed of calcifying shoulder tendinitis diagnosed by a medical specialist (rehabilitation, orthopedic surgeon or rheumatologist) by x-ray
* with disease evolution of more than 3 months and less than 12 months
* that give their informed consent by writing
Exclusion Criteria
* Patients with shoulder affections treated with shockwaves or corticosteroid injections.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
PRODUCTOS SANITARIOS ECA-RVB SLI
UNKNOWN
Consorci Sanitari del Maresme
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Lluís Guirao
PhD
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Consorci Sanitari del Maresme
Mataró, Barcelona, Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
46/16
Identifier Type: -
Identifier Source: org_study_id