Dry Needling Effectiveness of Patients on Break Anterior Cruciate Ligament.
NCT ID: NCT02699411
Last Updated: 2016-03-04
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
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Recruitment Status
UNKNOWN
Clinical Phase
NA
Total Enrollment
40 participants
Study Classification
INTERVENTIONAL
Study Start Date
2016-02-29
Study Completion Date
2016-09-30
Brief Summary
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We will conduct a randomized clinical trial observing forty patients divided into two groups: one group composed of twenty individuals undergoing surgery for ruptured ACL, which perform dry needling of myofascial trigger (PGM) point of the vastus muscle and then perform techniques proprioception (group a); and twenty patients not be treated with dry needling after ACL surgery, using only proprioceptive exercises to the joint (group B).
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Detailed Description
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It carries out a last fifteen days ECA surgical reconstruction of the anterior cruciate ligament. Twenty individuals in a group to be subjected to a technique of physiotherapy, dry needling were included. (Group A). Another group of twenty patients treated with conservative treatment performed a stability exercises and proprioception (Group B). Forty-six patients will be examined s. None had been previously operated by joint instability and all subjects were previously subjected to a diagnostic study by nuclear magnetic resonance before surgery and the diagnosis was confirmed by additional diagnostic testing. All patients will be evaluated by a physical therapist and Myofascial Trigger Point (PGM) of the vastus muscle will be evaluated.
patients using the following variables are evaluated:
* Pain: Visual Analog Scale (VAS) was used.
* Stiffness and physical function using the WOMAC scale (The Western Ontario and McMaster Universities Arthritis Index.).
* Range of motion of the knee joint: Scale ROM.
* Muscular strength, balance and propiocepción: Star Excursion by Balance Scale Test.
patients using the following variables are evaluated:
* Pain: Visual Analog Scale (VAS) was used.
* Stiffness and physical function using the WOMAC scale (The Western Ontario and McMaster Universities Arthritis Index.).
* Range of motion of the knee joint: Scale ROM.
* Muscular strength, balance and propiocepción: Star Excursion by Balance Scale Test.
Conditions
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Anterior Cruciate Ligament Reconstruction
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
PARALLEL
Primary Study Purpose
TREATMENT
Blinding Strategy
SINGLE
Investigators
Study Groups
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dry needling
Dry needling on the vastus is performed in patients undergoing ACL fortnight after the intervention and then evaluated. REL dry needling while supplies last twenty insertions before treatment, at midnight, a week and five weeks.
Group Type
ACTIVE_COMPARATOR
Dry needling
Intervention Type
DEVICE
dry needling Travell and Simons
Stability and propioception
Proprioception and stability exercises in patients undergoing ACL fortnight after the intervention and then evaluates performed before treatment, at midnight, a week and five weeks.
Group Type
ACTIVE_COMPARATOR
Stability and propioception
Intervention Type
OTHER
Start excursion balance test, WOMAC; ROM, EVA.
Interventions
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Dry needling
dry needling Travell and Simons
Intervention Type
DEVICE
Stability and propioception
Start excursion balance test, WOMAC; ROM, EVA.
Intervention Type
OTHER
Eligibility Criteria
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Inclusion Criteria
* over eighteen and anatomically mature surgically break LCA and valued above using MRI and functional tests to confirm the rupture of the ligament.
Exclusion Criteria
* Patients who did not reach 18 years of age and those over 55,
* postoperative complications
* cause myofascial or neuropathic pain in the lower limb, as lumba-sacral radiculopathy, neuropraxia, neurotmesis, axonotmesis or meralgia paresthetica;
* fibromyalgia.
* hypothyroidism
* iron deficiencies and patients who had a fear of needles (fear of needles).
* Lower limb differences.
* postoperative complications
* cause myofascial or neuropathic pain in the lower limb, as lumba-sacral radiculopathy, neuropraxia, neurotmesis, axonotmesis or meralgia paresthetica;
* fibromyalgia.
* hypothyroidism
* iron deficiencies and patients who had a fear of needles (fear of needles).
* Lower limb differences.
Minimum Eligible Age
18 Years
Maximum Eligible Age
55 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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European University Spain
OTHER
Sponsor Role
lead
Responsible Party
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Jorge Velázquez Saornil
Physiotherapist
Responsibility Role
PRINCIPAL_INVESTIGATOR
Principal Investigators
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Jorge Velázquez, Sr
Role: PRINCIPAL_INVESTIGATOR
European University
Locations
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Jorge Velázquez Saornil
Madrid, , Spain
Site Status
RECRUITING
Countries
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Spain
Central Contacts
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Facility Contacts
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Jorge Velázquez, Mr
Role: primary
References
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Other Identifiers
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European University
Identifier Type: -
Identifier Source: org_study_id
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