Status:

ENROLLING_BY_INVITATION

Healing After Augmentation of Alveolar Ridge Using Collagen Membrane

Lead Sponsor:

University of Belgrade

Conditions:

Bone Healing

Augmentation

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

One of the prerequisites for successful prosthetic implant therapy of patients is achieving the initial stability of the embedded implant, which largely depends on the width alveolar ridge, at the pla...

Detailed Description

The physiological process of bone tissue resorption after tooth extraction results in significant by changing the initial dimension of the alveolar ridge, due to horizontal and vertical resorption of ...

Eligibility Criteria

Inclusion

  • ASA I classification of health status,
  • Non-smokers or consumption of up to 10 cigarettes per day,
  • No signs of gingival inflammation,
  • Late installation of implants,
  • The possibility of achieving the primary stability of the implant,
  • The dimension of the residual alveolar ridge for implant placement ≥5 mm wide, height ≥12 mm,
  • Diagnosed fenestration, dehiscence of buccal bony lamella ≤3 mm in size and/or thickness of buccal bone lamella ≤1.5 mm,
  • Plaque index (PI) and gingival bleeding on provocation (KNP) \<15% and probing depth (DS) \<3 mm,
  • Preserved cemento-enamel border (CGG) without the presence of non-carious cervical lesions (NCL), or the presence of a defect in the root area up to 1mm deep with preserved CGG,
  • Preserved interjaw relationships.

Exclusion

  • Systemic acute administration of drugs up to 7 days before surgical intervention,
  • Systemic chronic administration of steroids or non-steroidal anti-inflammatory drugs,
  • History of oral surgical interventions in the last 4 months,
  • Poor oral hygiene,
  • Demonstrated hypersensitivity to collagen,
  • Pregnancy and breastfeeding,
  • Patient withdrawal from the research protocol in any evaluation period,
  • Patients who underwent standard augmentation of bone tissue with a substitute for bone and membrane, after implant installation,
  • Participation in clinical research in the last 6 months

Key Trial Info

Start Date :

March 7 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2029

Estimated Enrollment :

90 Patients enrolled

Trial Details

Trial ID

NCT06885983

Start Date

March 7 2025

End Date

November 1 2029

Last Update

March 25 2025

Active Locations (1)

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School of Sental Medicine

Belgrade, Serbia, 011