Clinical Trials Logo
  1. Home
  2. Oral Soft Tissue Conditions
  3. NCT02513368

Peri Implant Soft Tissue Healing in Single Implant Restoration Using Two Different Techniques

Oral Soft Tissue Conditions Clinical Trial

Official title:
Peri Implant Soft Tissue Healing in Single Implant Restoration Using the Guided Bone Regeneration Technique Ore a Connective Tissue Graft

Clinical Trial Summary

The aim of the present study was to propose the employment of Bio-Oss® and Bio-Gide® at implant site in order to evaluate if the increased bucco-lingual bone thickness could enhance the stability of peri implant soft tissue, when compared to the grafting technique ( bilaminar technique), performed in association with implant placement .

Clinical Trial Description

With respect to the soft tissue management many surgical approaches have been described in order to increase soft tissue volume and keratinized tissue height at implant site: roll flaps, connective tissue graft , epithelial connective tissue graft. In recent years, soft tissue substitutes , such as acellular dermal matrix or collagen matrix have been proposed to increase the dimensions of peri implant soft tissues; however, further studies have demonstrated that the allograft materials were less effective and less predictable than autogenous soft tissue grafts, in terms of increasing attached keratinized tissue , due to the considerable shrinkage and inconsistent quality of the attached tissue gained ; consequently soft tissue graft from the palate are currently considered the gold standard for augmenting peri implant soft. Some clinical studies proposed the association of contour augmentation by guided bone regeneration (GBR) with implant placement. The aim of these procedures is to restore the missing volume and to establish a facial bone wall of sufficient height and thickness to serve as a support for peri implant soft tissues; in these terms, GBR could be considered important to increase the stability of peri implant soft tissue , preventing the marginal soft tissue shrinkage and the following exposition of implant . This could be a valid approach to stabilize coronal peri implant soft tissue and at the same time less traumatic than grafting procedures. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02513368
Study type Interventional
Source University of Firenze and Siena, Napoli, Italy
Contact
Status Completed
Phase Phase 2
Start date January 2011
Completion date March 2014
View Details
See also
  Status Clinical Trial Phase
Completed NCT04918563 - Endothelium Dependent and Non-dependent Vasodilatation in Human Gingiva N/A
Active, not recruiting NCT06454084 - Investigation of Endothelium-dependent Vasodilation in Human Gingiva N/A
Completed NCT06238154 - Flurbiprofen Tablet vs Spray In Oral Soft Tissue Wounds Phase 4
Not yet recruiting NCT03717389 - The Prevalence of Soft Tissue Calcifications in the Head and Neck Region Using CBCT Among Egyptian Population
Completed NCT04131283 - Evidence of Spreading Vasoconstriction in Human Gingiva N/A
Not yet recruiting NCT06052501 - 3D Evaluation of the Lip Support in a Full-arch Implant-supported Rehabilitations
Completed NCT03605095 - Evidence of Spreading Vasodilation in Human Gingiva N/A
Completed NCT03335683 - Phytotherapy Agent in Third Molar Surgery Phase 4
Recruiting NCT06029322 - Collagen Matrix Versus Collagen Membrane as Socket Seal in ARP N/A
Completed NCT04276129 - Early Healing of Oral Soft Tissues: a Clinical and Biomolecular Analysis. Part II N/A
Completed NCT04865952 - Early Healing of Oral Soft Tissues: a Clinical and Biomolecular Analysis. Part III N/A
Completed NCT04202822 - Early Healing of Oral Soft Tissues: a Clinical and Biomolecular Analysis. Part I N/A