Skip to content

Development and Preliminary Clinical Application of Modified Anchor Nail

Development and Preliminary Clinical Application of Modified Anchor Nail

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONN-17013404
Enrollment
Unknown
Registered
2017-11-16
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-11-20

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

Conditions

Temporomandibular joint disorder

Interventions

A:TMJ anchorage
B:TMJ anchorage
C:TMJ anchorage

Sponsors

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

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) subjects over 12 years old, without sex limitation; (2) indication of TMJ anchorage; (3) patients did not participate in other clinical verifier within 3 months; (4) no acute infectious diseases, psychosis, systemic diseases; (5) volunteers and signed informed consent.;Inclusion criteria: (1) subjects over 12 years old, without sex limitation; (2) indication of TMJ anchorage; (3) patients did not participate in other clinical verifier within 3 months; (4) no acute infectious diseases, psychosis, systemic diseases; (5) volunteers and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) patients with allergy to titanium alloy; (2) acute or severe infection or chronic infection in the acute stage of patients; (3) surgery resulted in extensive soft tissue defects, and there was not enough soft tissue coverage in the wound after operation; (4) radioactive osteomyelitis, chronic osteomyelitis, osteoporosis; (5) primary disease of heart, lung, brain, kidney and other important organs; (6) in patients with mental disorders; (7) pregnant and lactating female; (8) patients unable to cooperate with treatment; (9)patients with advanced malignant tumor, tumor metastasis, tumor recurrence; (10) Condition of patient is so critical that is hard to evaluate the effectiveness and safety of the prosthesis.;Exclusion criteria: (1) patients with allergy to titanium alloy; (2) acute or severe infection or chronic infection in the acute stage of patients; (3) surgery resulted in extensive soft tissue defects, and there was not enough soft tissue coverage in the wound after operation; (4) radioactive osteomyelitis, chronic osteomyelitis, osteoporosis; (5) primary disease of heart, lung, brain, kidney and other important organs; (6) in patients with mental disorders; (7) pregnant and lactating female; (8) patients unable to cooperate with treatment; (9)patients with advanced malignant tumor, tumor metastasis, tumor recurrence; (10) Condition of patient is so critical that is hard to evaluate the effectiveness and safety of the prosthesis.

Design outcomes

Primary

MeasureTime frame
successful rate;mouth opening;pain;;successful rate;mouth opening;pain;

Countries

China

Contacts

Public ContactShanyong Zhang;Shanyong Zhang ;

Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University;Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University

zhangshanyong@126.com;zhangshanyong@126.com+86 13817673406;+86 13817673406

Outcome results

None listed

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