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Electronic bite force-measuring device clinical application effect and safety evaluation

Electronic bite force-measuring device clinical application effect and safety evaluation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-BON-17010878
Enrollment
Unknown
Registered
2017-03-15
Start date
2017-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

None listed

Interventions

Sponsors

Stomatological hospital of Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) the participants agreed to participate in this experiment, and sign the informed consent form (only after all the relevant steps); (2) the subjects for hospital dental clinic patients; (3) aged 18 to 60 years old, men and women not limited; (4) the three months to other medical devices clinical trials or clinical trials; (5) on the mandibular anterior teeth with no apparent tooth defect, loose degree is normal; (6) a complete occlusion relation.

Exclusion criteria

Exclusion criteria: (1) anterior tooth area open jaws, underbite, deep draping or deep cover; (2) the maxillary or mandibular anterior teeth area for the activities of denture; (3) to the plastic, articulating paper material has a history of allergic reaction; (4) other researchers think unfavorable to participants.

Design outcomes

Primary

MeasureTime frame
Jaw teeth before the tooth tip stagger position (ICP) on the upper front teeth contact and the number of teeth;

Countries

China

Contacts

Public ContactZHOU CHONGYANG

Stomatological hospital of Peking University

chongyangzh@sina.com+86 13651164927

Outcome results

None listed

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