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Feasibility Study on Dynamic Ultrasound Observation of the Pathogenesis of Hip Impingement Syndrome

Feasibility Study on Dynamic Ultrasound Observation of the Pathogenesis of Hip Impingement Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125330
Enrollment
Unknown
Registered
2026-05-25
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

The specific disease investigated in this study is hip pain syndrome characterized primarily by chronic groin pain, in which patients present with groin pain and hip functional impairment lasting more than 3 months, with symptoms reproducible or exacerbated under standardized provocative maneuvers including the FADIR maneuver, HEC test, and modified Thomas test. The underlying etiology in the stud

Interventions

Hip Pain Patient Group:Hip Pain
Healthy control group:None

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Hip Pain Patient Group: (1) Main complaint is pain in the inguinal region, duration >=3 months; (2) Age 18–60 years; (3) Passed preliminary movement tests: active hip extension >=5°, passive hip flexion >=90° (NRS = Grade 2. 2. Healthy Control Group: (1) No history of hip/groin pain within the past 12 months; (2) Aged 18–60 years; (3) Matched with the patient group in terms of gender frequency; the comparability of age distribution between the two groups will be statistically tested in baseline analysis; (4) Required to perform preparatory movements as per the patient group.

Exclusion criteria

Exclusion criteria: 1. Identify organic hip joint diseases: (1) surgical history of the affected hip joint; (2) acute traumatic hip joint injury within the past 6 months; (3) severe osteoarthritis (Toennis grade >=2); (4) hip dysplasia (CE angle =2 positive results in the straight leg elevation test and Kemp test, and negative hip joint signs). 3. Impact on examination quality: (1) Injection of corticosteroids/hyaluronic acid/local anesthetics into the affected hip joint cavity or iliopsoas tendon sheath within the past 6 months; (2) The pre-evaluation of the image quality of the groin area in the preparatory movement test is rated as level 3 (poor); (3) Skin damage or infection in the inguinal region; (4) Pregnancy/lactation period; (5) Failed to pass the preparatory action test; (6) Refusal to sign informed consent form.

Design outcomes

Primary

MeasureTime frame
Changes in distance between iliopsoas tendon and labrum (? d);

Secondary

MeasureTime frame
AI labrum segmentation performance (AUC);MRI registration accuracy;Feasibility rate of 3D reconstruction;

Countries

China

Contacts

Public ContactLin Jianhao

Peking University People's Hospital

linjianhao@pkuph.edu.cn+86 10 8832 6666

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026