Effectiveness of Dry Needling and STM on Pain Management for Anterior Cruciate Ligament Reconstruction (ACLR)
NCT ID: NCT03506685
Last Updated: 2025-09-23
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
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WITHDRAWN
NA
INTERVENTIONAL
2018-06-01
2019-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
TREATMENT
SINGLE
Study Groups
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control group Standard ACL protocol
This group will receive the standard ACL protocol rehab
No interventions assigned to this group
Dry needling and STM group
This group will also receive the standard ACL protocol in addition to STM and DN
Dry needling and STM
dry needling and soft tissue mobilization
Interventions
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Dry needling and STM
dry needling and soft tissue mobilization
Eligibility Criteria
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Inclusion Criteria
* Scheduled for ACL Reconstruction Surgery
Exclusion Criteria
* History of blood borne pathogens/infectious disease/active infection/metal allergy
* Bleeding disorders or currently taking anti-coagulant medications
* Participants who are not fluent in English
18 Years
40 Years
ALL
No
Sponsors
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Keller Army Community Hospital
FED
Responsible Party
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Jamie Morris
principal Investigator
Locations
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Keller Army Community Hospital
West Point, New York, United States
Countries
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Other Identifiers
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18KACH002
Identifier Type: -
Identifier Source: org_study_id
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