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Application of Palatal bone graft in dental implants

Evaluation of the success rate of dental implants after Alveolar buccal cortex Reconstruction using Palatal bone graft

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221111056472N1
Enrollment
15
Registered
2022-12-15
Start date
2022-12-22
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Placement of dental implants in the anterior of the maxilla after reconstruction of the buccal cortex using palatal bone grafting.

Interventions

Intervention group: In 15 patients who visited the oral, maxillofacial surgeon's office, after teeth extraction and implant placement with the standard protocol, the palatal bone graft will be harvest

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: candidate to receive an implant in the anterior of the maxilla (incisors) Loss of buccal cortex of implant during surgery up to half of the implant Intactness of other bone walls Availability of palatal bone for transplantation Intact soft tissue for implant coverage The patient's health in terms of systemic issues

Exclusion criteria

Exclusion criteria: Non-cooperation of the patient in terms of compliance with health issues Failure to visit the patient for follow-up Previous surgical history of the desired area

Design outcomes

Primary

MeasureTime frame
The amount of bone loss. Timepoint: Three months and six months after surgery. Method of measurement: Periapical radiograph.;Implant success. Timepoint: Three months and six months after surgery. Method of measurement: observation.;Probing depth of the pocket on the buccal surface of the implant. Timepoint: Three months and six months after surgery. Method of measurement: Michigan-O periodontal probe William's Color Coded Marking.;Wound dehiscence. Timepoint: Three months and six months after surgery. Method of measurement: observation.;Wound infection. Timepoint: Three months and six months after surgery. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Seydabadi

Semnan University of Medical Sciences

parisaseydabadi6@gmail.com+98 23 3334 2127

Outcome results

None listed

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