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The effect of the dry needle on pain and range of motion after anterior cruciate ligament reconstruction

Evaluation of the added effect of quadriceps dry needling on knee range of motion and pain in the primary phase of rehabilitation after anterior cruciate ligament reconstruction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181209041898N1
Enrollment
24
Registered
2019-02-26
Start date
2019-05-22
Completion date
Unknown
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Athletes who performed anterior cruciate ligament reconstruction surgery. Sprain of cruciate ligament of knee

Interventions

Intervention 1: Intervention group 1: receiving 12 sessions (four weeks) of routine knee physiotherapy and one session of quadriceps dry needle in each week. Intervention 2: Intervention group 2: rece

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Age between 18 to 45 years Athletes with knee anterior cruciate ligament injury that is created during sportive activities undergoing ACL surgery and being referred to physiotherapy by a specialist, within two weeks after surgery using hamstring grafts for surgery knee flexion of 90 degrees or less when referring to physiotherapy clinic (2 weeks after surgery) level 6 to 9 according to Tagner Questionnaire

Exclusion criteria

Exclusion criteria: contraindications of the dry needle including fear of needle, diabetes, using anticoagulant drugs, and etc. any history of lower limb disorder or fracture prior to surgery that had limited knee range of motion Neuropathic pain or acute phase of local infection in lower extremity

Design outcomes

Primary

MeasureTime frame
Knee range of motion. Timepoint: at the beginning of the study and 7, 14, 21, and 28 days after the initiation of treatment. Method of measurement: Goniometery.

Secondary

MeasureTime frame
Pain intensity. Timepoint: at the beginning of the study and 7, 14, 21, and 28 days after the initiation of treatment. Method of measurement: Numerical rating scale of pain.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Rzaeghi

Shiraz University of Medical Sciences

razeghm@sums.ac.ir+98 71 3627 1551

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026