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Design, fabrication and application of occlusal recording cap for implant-supported fixed prostheses

Design, fabrication and application of occlusal recording cap for implant-supported fixed prostheses

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041154
Enrollment
Unknown
Registered
2020-12-19
Start date
2020-12-25
Completion date
Unknown
Last updated
2021-03-01

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

Conditions

Dentition defect

Interventions

Experimental group:Using occlusal recording cap in determining occlusal relationship
Control group:Using only silicone rubber material in determining occlusal relationship

Sponsors

Peking University stomatological hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Subjects not less than 20 years old; 2. Subjects with dentition defect of 2 or more posterior teeth (Kennedy I or II); 3. Subjects with no obvious abnormal occlusion (no early contact, occlusion interference) and no clinical symptoms before restoration; 4. Subjects with periodontal health or with perfect periodontal treatment system; 5. Patients who have signed informed consent; 6. Subjects without any local or systemic diseases contraindicated by implant surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with missing dentition or loss of occlusal relationship of residual teeth; 2. Patients with temporomandibular joint disease; 3. Subjects with oral side effects; 4. Pregnant and lactating women; 5. Subjects who smoked more than 10 cigarettes / day; 6. Subjects taking steroids or bisphosphonates; 7. Patients with physical disability or mental illness that affect oral health care; 8. Patients with a history of chemotherapy within 5 years before operation, or patients with a history of radiotherapy in the head and neck region; 9. There are situations that affect the completion of the study or interfere with the analysis results of the study, such as non cooperation and concealment of medical history.

Design outcomes

Primary

MeasureTime frame
Volume of occlusal adjustment;

Secondary

MeasureTime frame
Occlusal adjustment time;The proportion of lateral occlusal interference;Occlusion score of implant prosthese;Relative occlusal forces of implant prostheses;Visual analogue scale score;Average distance of occlusal planes between natural teeth in upper and lower jaw ;The deviation value of occlusal relationship;The consistency ratio of occlusal contact points;Complication rate;

Countries

China

Contacts

Public ContactDing Qian

Peking University stomatological hospital

dingqian.623@163.com+86 15120033697

Outcome results

None listed

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