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Assessment of the Long-Term Survival of Dental Implants in Cleft Patients

Assessment of the Long-Term Survival of Dental Implants in Cleft Patients - Dental Implant survival in cleft patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON56834
Enrollment
69
Registered
2021-06-10
Start date
2021-06-17
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Kaakchirurgische ingrepen, implantologie harelip orofacial cleft

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. At least 18 years old. 2. Has been treated for cleft condition. 3. Received a dental implant in replacement of one or more of the maxillary incisors or canine.

Exclusion criteria

Exclusion criteria: 1. Disability (mental and/or physical) to maintain basic oral hygiene procedures 2. Condition which affects the healing of bone. 3. Patients unwilling or incapable of understanding and signing the informed consent for secondary measurements.

Design outcomes

Primary

MeasureTime frame
From the patients who received a dental implant data will be retrospectively collected about when they received the implant, possible parameters which could impact the survival rate (smoking, oral hygiene, length of dental implant, diameter of dental implant, interval between secondary cleft repair and implant placement, interval between tertiary cleft repair and implant placement, type of tertiary cleft repair (horizontal, vertical or both)), and the date of failure if there was an indication of removal of dental implant or indication that the dental implant lost functionality.

Secondary

MeasureTime frame
From the patients who received a dental implant data will be prospectively collected. The patients will be visiting once. During this visit a calibrated periodontal probe will be used to measure BoP and PD, a radiograph of the implant will be taken using a standardized method and PROM will be measured using the Dutch translation of the Oral Health Impact Profile (OHIP- NL49) for the situation before and after implantation of an dental implant.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)