Status:

UNKNOWN

Comparison of Peri Implant Soft Tissue Esthetics With Immediate Temporization With and Without Subepithelial Connective Tissue Graft

Lead Sponsor:

Cairo University

Conditions:

Immediate Temporization and Soft Tissue Augmentation Around Delayed Implants

Eligibility:

All Genders

18-60 years

Phase:

PHASE3

Brief Summary

The aim of this study is to clinically evaluate peri-implant soft tissue esthetics around single delayed implants in the esthetic zone.

Detailed Description

To compare the efficacy of soft tissue augmentation on the peri-implant soft tissue esthetics along with immediate temporization to immediate temporization only. Population (P): patients with a singl...

Eligibility Criteria

Inclusion

  • Age \> 18 years old
  • Good medical and psychological health
  • Absence of untreated caries lesions and untreated/uncontrolled periodontal disease. If patients required periodontal treatment (non-surgical and/or surgical), this was arranged outside the study protocol and completed at least 30 days prior to the enrolment
  • Need of a single-tooth replacement in the aesthetic (incisor, canine or premolar) region
  • Willingness to sign the informed consent form

Exclusion

  • Any known disease (not including controlled diabetes mellitus), infections or recent surgical procedures within 30 days of study initiation;
  • Chronic treatment (i.e., 2 weeks or more) with any medication known to affect oral status (e.g., phenytoin, dihydropyridine, calcium antagonists and cyclosporine) within 1 month before baseline visit;
  • Anticoagulant therapy with warfarin, clopidogrel, ticlopidine or once daily aspirin (more than 81 mg);
  • HIV or Hepatitis;
  • Physical handicaps that would interfere with the ability to perform adequate oral hygiene;
  • Alcoholism or chronic drug abuse;
  • Heavy smokers (\>10/cigarettes per day);
  • Lack of adequate primary stability at implant insertion that enables immediate provisionalization (insertion torque ca 30 Ncm).

Key Trial Info

Start Date :

December 1 2018

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2020

Estimated Enrollment :

22 Patients enrolled

Trial Details

Trial ID

NCT03770975

Start Date

December 1 2018

End Date

May 1 2020

Last Update

December 10 2018

Active Locations (1)

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Faculty of Dentistry, Cairo University

Cairo, Egypt