Skip to main content
Clinical Trials/NCT06842277
NCT06842277CompletedPhase 2

Reconstruction of Deficient Interdental Papilla Using Albumin-platelets Rich Fibrin- A Case Series

Cairo University2 sites in 1 country10 target enrollmentStarted: February 18, 2025Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
10
Locations
2
Primary Endpoint
Distance between contact point and papilla tip (Height of black triangle)

Study Overview

Brief Summary

The goal of this ( A case series, clinical trial ) is treatment of deficient interdental papilla in patients who have interdental papillary loss class 1 or 2 in maxillary or mandibular anterior region with plaque index and gingival index less than 1 and the selected sites had distance between contact point and inter proximal bone crest less than 7mm and probing depth less than 4mm.

Hypothesis:

Albumin-PRF is an efficient treatment of deficient interdental papilla. The primary outcome ( distance between the contact point and papillary tip will be measured by periodontal probe) The participants will practice good oral hygiene measures

Detailed Description

The goal of this ( A case series , clinical trial ) treating patients whose complaint from poor esthetics and unappealing black triangles inn anterior sextant using an autogenous , biocompatible material ( Albumin platelets rich fibrin).

The selected patients had well -aligned maxillary teeth, no caries, no proximal restoration, fixed prosthesis, or any orthodontic appliance, at least one class 1or 2 interdental papilla loss in maxillary or mandibular anterior regions and at selected sites, distance between contact point and inter proximal bone crest less than 7mm and probing depth less than 4mm.

Also patients had plaque index and gingival index less than 1. Patients whose had advanced periodontal problems (advanced bone and soft tissue loss), a systemic condition affect blood components and healing, smokers and Patients who are pregnant will be excluded.

For all patients, full mouth scaling and root planing will be done, measuring probing depth, taking periapical radiograph for the target sites and taking rubber base impression will be done.

Operation phase:

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients' complaint from poor esthetics and unappealing black triangles in anterior sextant.
  • •Patients had well -aligned maxillary teeth, no caries, no proximal restoration, fixed prosthesis, or any orthodontic appliance.
  • •Patients had at least one class 1or 2 interdental papilla loss in maxillary or mandibular anterior regions.
  • •Patients had at selected sites, distance between contact point and inter proximal bone crest less than 7mm and probing depth less than 4mm.
  • •Patients had plaque index and gingival index less than 1.

Exclusion Criteria

  • •Patient had advanced periodontal problems (advanced bone and soft tissue loss).
  • •Patients had a systemic condition affect blood components and healing.
  • •Smoker patients.
  • •Patients who are pregnant.

Arms & Interventions

patients whose had deficient interdental papilla

Other

treatment of patients whose had deficient interdental papilla using injectable Albumin -platelets rich fibrin

Intervention: Injectable albumin platelets rich fibrin (Biological)

Outcomes

Primary Outcomes

Distance between contact point and papilla tip (Height of black triangle)

Time Frame: 6 months

The distances between the contact point and papilla tip will be measured clinically by a periodontal probe

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Eman Salah Eldin Mahmoud Radwan

Master Student

Cairo University

Study Sites (2)

Loading locations...

Similar Trials