Subepithelial Connective Tissue Graft Versus Amniotic Chorion Membrane for Peri-implant Mucosal Thickness Enhancement

Tanta University

Status

Not yet enrolling

Conditions

Dental Implant

Treatments

Procedure: implant placement and soft tissue augmentation with Autogenous Subepithelial Connective Tissue Graft or Amniotic Chorion Membrane

Study type

Interventional

Funder types

Other

Identifiers

NCT06295653

7-23

Details and patient eligibility

About

The objective of this study will be to assess the efficacy of the peri-implant mucosal thickness enhancement following either subepithelial connective tissue grafts or Amnion Chorion Membrane placed simultaneously with dental implant placement.

Enrollment

26 estimated patients

Sex

All

Ages

30 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with good systemic health with no contraindication for periodontal surgery.
No history of any medications in the previous 6 months that may interfere with periodontal tissue health or healing.
Ability to maintain good oral hygiene as evidenced in recall visits.
Aged 30 to 55 years.
Stable periodontal condition and missing one single tooth (maxillary anterior teeth and premolars) with adjacent teeth present and thin mucosal phenotype (< 2mm bucco- lingual thickness).

Exclusion criteria

Medically compromised patients and systemic conditions precluding periodontal surgery.
Smokers.
Severe hematologic disorders (e.g., hemophilia or leukemia), uncontrolled infectious or metabolic diseases that could compromise normal healing, liver, or kidney dysfunction/failure.
Patients subjected to irradiation in the head and neck area.
Patients treated or under treatment with intravenous amino bisphosphonates.
Patient affected by active periodontitis or has poor oral hygiene and motivation.
Uncontrolled diabetes mellitus.
Pregnant women or planning become pregnant, and nursing mothers.