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ultrasound guided dry needling for jumper's knee

OUTCOME COMPARISON OF ULTRASOUND GUIDED DRY NEEDLING IN ADDITION TO CONVENTIONAL PHYSICAL THERAPY FOR TREATMENT OF PATIENTS WITH JUMPER’S KNEE

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210409050913N1
Enrollment
96
Registered
2021-04-17
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Jumper's knee. Patellar tendinitis

Interventions

Intervention 1: Intervention group: Ultrasound guided dry needling in addition to routine physical therapy. each session of ultrasound guided dry needling will consist of three needle insertions last

Sponsors

The University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Athletes with medical diagnosis of patellar tendinopathy and anterior knee pain located on the inferior pole of the patella for over 1 month. The intensity of pain of 3.0 or greater on a 0-to-10 visual analog scale while walking up and down stairs and high pain intensity in single leg decline squat test. Palpation tenderness of the superior insertion of the patellar tendon. Athletes of either genders Age ranges between 18 to 45 years. A score below 80 on the Victorian Institute of Sports Assessment for PT (VISA-P) questionnaire. Pain provocation on Single leg decline squat test as a score >0 on the NRS.

Exclusion criteria

Exclusion criteria: Knee surgery within the previous 6 months. Chronic knee joint diseases. Corticosteroid injection in the patellar tendon within the last 1 month. Contraindications for needling such as allergies/sensitivities, diseases/conditions, implants, areas of acute inflammation, acute systemic infections, on blood thinner or anticoagulants, with known history of bleeding disorders. Presence of multiple focal areas of calcification within the proximal tendon or radiographic fractures around the knee. Use of analgesics for last 48 hours. Any other concomitant treatment for jumper’s knee.

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: baseline, 1st, 2nd, and 4th week after the intervention. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Functional disability. Timepoint: baseline, 1st, 2nd and 4th week after the intervention. Method of measurement: VISA-P Score, KOOS Score, Lysholm score.

Countries

Pakistan

Contacts

Public ContactFaiza Sharif

The University of Lahore

faiza.sharif@uipt.uol.edu.pk+92 42 35322501

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026