Factors affecting reduction accuracy and complications of intracapsular condylar fractures and corresponding measures

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2600127754

Enrollment

Unknown

Registered

2026-07-07

Start date

2026-04-01

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

Intracapsular Condylar Fractures

Interventions

Case series:None

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed as intracapsular condylar fracture by preoperative clinical manifestations and CBCT examination; 2.Patients who did not receive any treatment prior to admission; 3.All patients had no facial paralysis, joint disease or ankylosis before fracture.

Exclusion criteria

Exclusion criteria: 1.Patients with recurrent or old intracapsular condylar fractures; 2.Patients who have failed closed therapy or failed surgical treatment; 3.Patients with incomplete clinical data; 4.Unable to cooperate with follow-up visits and follow-up visits.

Design outcomes

Primary

Measure	Time frame
Openness;	—

Secondary

Measure	Time frame
Facial nerve symptoms;occlusal disorder;Temporomandibular joint symptoms;condyle morphology;	—

Countries

China

Contacts

Public ContactShuai Li

The Affiliated Stomatological Hospital of GuangXi Medical University

kqyyls@163.com+86 13217811915

Outcome results

None listed

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