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A self-controlled study on the effect of unilateral condylar resorption on alveolar bone

The effect of unilateral condylar resorption on alveolar bone: A prospective self-controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112563
Enrollment
Unknown
Registered
2025-11-17
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Condylar resorption

Interventions

Control group:None
Exposure group:None

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 20 Years

Inclusion criteria

Inclusion criteria: 1.Age: 12 to 20 years old (inclusive of 12 and 20 years old); 2.The patient require to extract the lower impacted third molar; 3.The patient was confirmed by joint MRI diagnosis that one side was a normal joint and the other side had idiopathic condylar resorption (Young's grade 2 or above). 4.The patient voluntarily participated in the study, could cooperate with the examination and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.The patient has obvious oral abscesses, precancerous lesions, fungal infections and pericoronitis of wisdom teeth throughout the mouth. 2.The patient has at least one of the following diseases: juvenile idiopathic arthritis and osteoarthritis, autoimmune diseases, endocrine disorders, anorexia nervosa, diabetes and thyroid diseases; 3.The patient has a history of intravenous use of bisphosphonates. 4.The patient uses immunosuppressants; 5.The patient has coagulation dysfunction, thrombocytopenia, hemophilia or significant anemia. 6.The patient has malignant tumor. 7.The patients diagnosed with acquired immunodeficiency syndrome, syphilis, hepatitis B and hepatitis C, who have not received standardized treatment and control; 8.According to the researcher's judgment, the patient has other factors that may affect the research results or lead to the forced termination of this study halfway, such as pregnancy, lactation, alcohol abuse, drug abuse, other serious diseases (including mental illness) requiring combined treatment, severe laboratory test abnormalities, accompanied by family or social factors, etc., which will affect the patient's safety.

Design outcomes

Primary

MeasureTime frame
The main differential genes of the alveolar bone between the affected side and the healthy side.;

Secondary

MeasureTime frame
The differential protein enrichment pathways of alveolar bone between the affected side and the healthy side;The differential gene enrichment pathways of alveolar bone between the affected side and the healthy side.;

Countries

China

Contacts

Public ContactJing Ge

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

2044328567@qq.com+86 21 2327 1699

Outcome results

None listed

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