Wound Dehiscence Clinical Trial
Official title:
Flipped Autograft: a Novel Approach for Management of Wound Dehiscence in Implant Dentistry
NCT number | NCT05513222 |
Other study ID # | hamdy |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 22, 2021 |
Est. completion date | April 27, 2022 |
Verified date | March 2024 |
Source | Ain Shams University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This case report describes a novel technique for management of peri-implant wound dehiscence that involves using auto graft from the same surgical site to seal the dehiscence defect.
Status | Completed |
Enrollment | 10 |
Est. completion date | April 27, 2022 |
Est. primary completion date | January 29, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Adult patients in a healthy systemic condition. 2. Both genders 3. Patients should have single missing tooth. 4. Seibert Class I ridge defect. 5. Patients should approve to deliver a signature to a written consent after study nature explanation. Exclusion Criteria: - 1- Patients with any smoking habits. 2- Pregnant females, decisional impaired individuals, Prisoners and handicapped patients. 3- Patients having poor oral hygiene or not wanting to carry out oral hygiene measures. 4- Patients with infections either periodontally or periapically. |
Country | Name | City | State |
---|---|---|---|
Egypt | Ahmed Hamdy | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University | British University In Egypt |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | complete primary intention healing of the wound dehiscence | complete uneventful healing will be assessed clinically by measuring soft tissue width and thickness using periodontal probe under local anesthesia | 3 months | |
Secondary | esthetic outcome and patient satisfaction. | esthetic outcome will be measured using pink esthetic score. Pink esthetic score (PES) will be recorded for five variables: "mesial papilla, distal papilla, curvature of the facial mucosa, level of the facial mucosa, and root convexity/soft tissue color and texture at the facial aspect of the implant site". A score of 2, 1, or 0 will be assigned to all five parameters.
also patient satisfaction will be recorded using: • (VAS) Visual analogue scale to measure postoperative pain. Pain score reported by the patient. directly through Visual Analogue Scale score (from 0 to 10. 0: no pain, 1: minimal pain, 5: moderate pain, 10: severe pain) which will be recorded after 2 weeks (Yildirim et al., 2017) |
3 months |
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