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Studying the effect of needling muscles attached to the iliotibial band on clinical symptoms of patients with iliotibial band syndrome

Comparing of the effect of gluteus maximus, gluteus medius, and tensor fascia lata muscle needling versus sham needling on the findings of clinical tests and symptoms in patients with iliotibial band syndrome: A randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160221026674N9
Enrollment
30
Registered
2026-01-24
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Iliotibial band syndrome. Iliotibial band syndrome

Interventions

Intervention 1: Intervention group:10 sessions of Burst TENS with a pulse frequency of 100 Hz and a burst frequency of 10 Hz, a pulse width of 200 microseconds, for 20 minutes10 sessions of continuous

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patients with iliotibial band syndrome in the subacute or chronic phase of the disease Aged between 18 and 45 years Presence of pain and tenderness (4 or higher on the numerical pain scale) at the site of attachment of the band to the lateral epicondyle of the femur Activity level 5 to 10 according to the Tegner scale

Exclusion criteria

Exclusion criteria: Body mass index greater than 30 Any orthopedic or neurological disorder A history of knee injury or history of knee physiotherapy in the previous 12 months Limited range of motion Fibromyalgia or chronic pain syndrome Systemic inflammatory diseases Corticosteroid injections or use of anti-inflammatory drugs in the past month Phobia of needles Use of anticoagulant drugs Uncontrolled diabetes Any musculoskeletal disorder in the lower extremities except iliotibial band syndrome

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before, one day after and two weeks after treatment. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Lower Limb Function. Timepoint: Before, one day after and two weeks after treatment. Method of measurement: Lower extremity functional scale.;The findings from the Rene, Noble, Uber, and modified Thomas diagnostic tests. Timepoint: Before, one day after and two weeks after treatment. Method of measurement: Positive or negative test result.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Mohamadi

Shiraz University of Medical Sciences

mohamadm@sums.ac.ir+98 71 3212 2600

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026