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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04400825
Other study ID # CEIm1955
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date July 19, 2020

Study information

Verified date November 2020
Source Universidad de Zaragoza
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hip osteoarthritis (OA) is one of the most prevalent chronic disease in the world. Currently several authors have shown the presence of active myofascial trigger points (MTrP) in the muscles surrounding the hip joint that reproduce the symptoms of the patients with hip OA. Despite of the beneficial effects that have shown may conservative non-pharmacological treatments, there is a lack of studies evaluating the effects of the conservative treatments on muscle extensibility. According to the new paradigm about the presence of MTrPs, the investigators decided to conduct a randomized clinical trial to compare the effects of DN intervention and stretching protocol on muscle extensibility in patients with hip OA.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date July 19, 2020
Est. primary completion date July 19, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria: - unilateral hip OA diagnosed medically with a X-Ray tess and following the American College of Rheumatology Criteria Exclusion Criteria: - Secondary osteoarthritis by a traumatism, Paget disease, inflammatory or metabolic disease, congenital diseases etc. - Vascular or neurological disease. - Musculoskeletal pathologies in lumbar spine, pelvis or lower limbs - DN contraindications or fear of needles

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Dry needling
Dry needling of the active MTrPs following the technique described by Hong et al (1994,1995)

Locations

Country Name City State
Spain Luis Ceballos Laita Soria

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Zaragoza

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary muscle extensibility the examiners assess the muscle extensibility using an inclinomenter Baseline
Primary muscle extensibility the examiners assess the muscle extensibility using an inclinomenter up to 3 weeks
Secondary Stiffness the examiners assess the stiffness using the WOMAC stiffness subscale Baseline
Secondary Stiffness the examiners assess the stiffness using the WOMAC stiffness subscale up to 3 weeks
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