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Ultrasonographic Imaging Features and Consistency with Surface Projections of Deep Gluteal Syndrome—An Observational Clinical Study

Ultrasonographic Imaging Features and Consistency with Surface Projections of Deep Gluteal Syndrome—An Observational Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127903
Enrollment
Unknown
Registered
2026-07-09
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Deep Gluteal Syndrome

Interventions

Patient group:None
Healthy control group:None

Sponsors

Zhejiang Provincial Hospital of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for the patient group: (1) The participant or their relatives voluntarily cooperate with the study and sign the informed consent form; (2) Age 18 or older, any gender; (3) Meet the above DGS diagnostic criteria; (4) Have not taken any anti-inflammatory or pain-relief medications or received treatment for hip symptoms in the past 15 days; (5) Stable vital signs, clear consciousness, able to communicate, and can cooperate with researchers to complete the relevant assessments. 2. Inclusion criteria for the healthy control group: (1) Age, gender, and BMI match the patient group. (2) No history of hip, buttock, or lower back pain or discomfort in the past year. (3) Physical examination is normal.

Exclusion criteria

Exclusion criteria: 1. For symptoms clearly caused by diseases in the lumbar spine, hip, or knee: patients with clear lumbar nerve root signs (like dermatomal sensory loss, muscle weakness, or abnormal reflexes); positive hip anesthesia test; abnormal gait in the knee, knee pain triggered by single-leg weight-bearing test, and referred hip pain, etc.; 2. Those who are unconscious or unable to clearly express their subjective discomfort; people with mental illnesses or substance abuse issues; those with severe anxiety or depression; patients with serious primary diseases in the cardiovascular, respiratory, digestive, or other systems; those with severe wasting diseases or progressive malignant tumors; patients with infections or bleeding disorders; 3. Pregnant women, breastfeeding women, and those planning to get pregnant in the last three months; 4. Those who have used other medications or interventions within the last 15 days; 5. People currently participating in other clinical trials that might affect the results of this study; 6. BMI over 35 kg/m^2.

Design outcomes

Primary

MeasureTime frame
Ultrasound feature parameters;Consistency of Surface Projection;

Secondary

MeasureTime frame
Modified Harris Hip Score;Visual Analogue Scale;

Countries

China

Contacts

Public ContactGuoqian Chen

Zhejiang Provincial Hospital of TCM

chenguoqian1991@163.com+86 571 8706 8001

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026