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Investigating the effect of acupuncture on pain and function in patients with patellofemoral pain syndrome

Investigating the effect of acupuncture on pain and function in patients with patellofemoral pain syndrome: a clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241118063761N1
Enrollment
50
Registered
2024-12-10
Start date
2024-12-23
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Patellofemoral Pain Syndrome. Patellofemoral disorders

Interventions

Intervention group: Nine acupuncture sessions, three sessions per week, one day in between.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 35 years Diagnosis of unilateral patellofemoral syndrome based on at least 5 of the 7 listed symptoms (pain elicited by at least two of the following four tests: (i) isometric muscle contraction with slight knee flexion, (ii) patellofemoral joint line palpation, (iii) patellar compression against the femur (IV) active resisted knee extension.)There is no evidence of other intra- or extra-articular knee injuries as determined by physical examination and radiographic evaluation intensity of 3 on the VAS scale, No history of knee trauma Intra-articular injection or physiotherapy within the last 3 months or surgery No use of non-steroidal anti-inflammatory drugs within 15 days prior to treatment Full cooperation with the study

Exclusion criteria

Exclusion criteria: Age outside the range of 18 to 35 years Diagnosis of Patellofemoral Pain Syndrome based on 5 or fewer out of 7 listed symptoms Presence of other intra-articular or extra-articular knee injuries Pain intensity less than 3 on the VAS scale History of knee injury, intra-articular injection, physiotherapy in the past 3 months, or surgery Use of non-steroidal anti-inflammatory drugs within 15 days prior to the start of treatment Lack of full cooperation with the study

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Immediately, one and three months after the intervention. Method of measurement: Visual Analogue Scale (VAS).

Secondary

MeasureTime frame
Score of Knee Injury and Osteoarthritis Outcome Score (KOOS). Timepoint: Immediately after the intervention, one and three months after the intervention. Method of measurement: Knee Injury and Osteoarthritis Outcome Score (KOOS).;Measuring time climbing stairs. Timepoint: Immediately after the intervention, one and three months after the intervention. Method of measurement: Digital Stopwatch.;?Single leg hop test. Timepoint: Immediately after the intervention, one and three months after the intervention. Method of measurement: Tape meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Mahdi Jafari

Iran University of Medical Sciences

jafarimohammadmehdi35@gmail.com+98 21 6435 2446

Outcome results

None listed

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