Status:

COMPLETED

Effect of Monolayer Versus Multilayer Leucocyte-Platelet Rich Fibrin (L-PRF) in Interdental Papillary Reconstruction

Lead Sponsor:

Ain Shams University

Conditions:

Recession

Eligibility:

All Genders

18-40 years

Phase:

NA

Brief Summary

The interdental papilla is very small but it has a great implication from an aesthetic view, more specifically in the anterior region because it is always displayed during smiling. The lack of interde...

Detailed Description

A total of 20 patients will be selected who are caring about esthetics and concerned to go through the management of eradication of "black triangles" by interdental papillae reconstruction in esthetic...

Eligibility Criteria

Inclusion

  • 1\. Patients diagnosed with black triangles. 2. Both genders aged from 18-40 years. 3. Patients should be systemically free. 4. Patients with Nordland's class I or II. Nordland and Tarnow classified the interdental papilla loss; the classification is based on three anatomic landmarks: the contact point interdentally, the coronal level of the CEJ interproximally and the facial apical level of the cemento-enamel junction (CEJ). \[Nordland WP, et al, 1998\] Four classes were identified
  • Normal: The interdental papilla fills up the whole embrasure to the interproximal contact point.
  • Class I: Presence of the tip of the papilla between interdental contact point and the interproximal CEJ.
  • Class II: Presence of the tip of the papilla at the interproximal CEJ or apical to it but still coronal to the facial CEJ.
  • Class III: Presence of the tip of papilla at similar plane with the labial CEJ or apical to it.
  • 5\. The vertical distance from the interdental contact point to the crest of the interdental bone is ≥ 6 mm as measured by bone sounding.
  • 6\. A band of keratinized tissue should be present around the test teeth ≥ 2 mm. 7. Gingival biotype of the area to be treated is ≥ 2 mm in thickness.

Exclusion

  • Acute periapical lesion.
  • moderate to severe form of periodontitis.
  • Pregnancy and lactation.
  • parafunctional habits.
  • Smoking, alcoholics or drug abusers.
  • Teeth with interdental spacing, rotation or inclination or crowding.
  • Vulnerable group of patients.

Key Trial Info

Start Date :

January 1 2016

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 1 2019

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT04091802

Start Date

January 1 2016

End Date

August 1 2019

Last Update

September 19 2019

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