Dry Needling Effectiveness of Patients on Break Anterior Cruciate Ligament.
ACL
1 other identifier
interventional
40
1 country
1
Brief Summary
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2016
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2016
CompletedFirst Submitted
Initial submission to the registry
February 26, 2016
CompletedFirst Posted
Study publicly available on registry
March 4, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2016
CompletedMarch 4, 2016
March 1, 2016
4 months
February 26, 2016
March 1, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Degree range of motion (ROM)
24 hours
Scores ofThe Western Ontario and McMaster Universities Arthritis Index (WOMAC)
24 hours
Pain scores visual analog scale (EVA)
24 hours
Scores of STAR BALANCE TEST
24
Secondary Outcomes (8)
Degree range of motion (ROM)
1 week
Degree range of motion (ROM)
5 weeks
Scores ofThe Western Ontario and McMaster Universities Arthritis Index (WOMAC)
1 week
Scores ofThe Western Ontario and McMaster Universities Arthritis Index (WOMAC)
5 weeks
Pain scores visual analog scale (EVA)
1 week
- +3 more secondary outcomes
Study Arms (2)
dry needling
ACTIVE COMPARATORDry 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.
Stability and propioception
ACTIVE COMPARATORProprioception and stability exercises in patients undergoing ACL fortnight after the intervention and then evaluates performed before treatment, at midnight, a week and five weeks.
Interventions
Start excursion balance test, WOMAC; ROM, EVA.
Eligibility Criteria
You may qualify if:
- over eighteen and anatomically mature surgically break LCA and valued above using MRI and functional tests to confirm the rupture of the ligament.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jorge VelĂ¡zquez Saornil
Madrid, Spain
Related Publications (47)
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PMID: 24567862BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jorge VelĂ¡zquez, Sr
European University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physiotherapist
Study Record Dates
First Submitted
February 26, 2016
First Posted
March 4, 2016
Study Start
February 1, 2016
Primary Completion
June 1, 2016
Study Completion
September 1, 2016
Last Updated
March 4, 2016
Record last verified: 2016-03
Data Sharing
- IPD Sharing
- Will not share