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Soft Tissue Augmentation clinical trials

View clinical trials related to Soft Tissue Augmentation.

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NCT ID: NCT06302387 Completed - Clinical trials for Soft Tissue Augmentation

Acellular Dermal Matrix Versus Tenting Technique in Peri-implant Soft Tissue Augmentation and Crestal Bone Stability

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

This study looks at two ways to make gums thicker and bones stable around dental implants for people with thin gums. It compares two methods in 40 people: one method uses a special graft, and the other uses a technique called tenting. The goal is to see which method might work better for making the gums and bones around implants healthier. The check-ups are planned when the implant is put in and again after one year. The study focuses on how these methods are done without talking about what the results are.

NCT ID: NCT06091605 Not yet recruiting - Dental Implants Clinical Trials

Evaluation of Omega Roll Envelope Flap for Soft Tissue Augmentation Around Osseointegrated Dental Implants

Start date: November 1, 2023
Phase: Phase 4
Study type: Interventional

Abstract Statement of the problem: Peri-implant soft-tissue augmentation procedures can be broadly divided into two groups, depending on their primary therapeutic objective: (1) Peri-implant soft-tissue phenotype modification and (2) Treatment of peri-implant marginal mucosa defects (PMMDs), also known as peri-implant soft-tissue dehiscences. Aim of the study: The aim of this study will be to evaluate the efficacy of the Omega roll envelope flap (OREF) technique compared to the conventional envelope split-thickness flap technique combined with an autogenous connective tissue graft, in enhancing Peri-implant soft tissue phenotype defined by the gingival thickness, keratinized tissue width, mucosal margin level and interproximal papilla height around implant.

NCT ID: NCT05119777 Completed - Clinical trials for Soft Tissue Augmentation

HArmonyCa Injectable Gel for Mid Face Soft Tissue Augmentation

HArmonyCa EUMD
Start date: October 13, 2021
Phase: Phase 4
Study type: Interventional

Prospective, open label, post marketing study of the safety and effectiveness of HArmonyCa injectable gel for mid-face soft tissue augmentation

NCT ID: NCT04367766 Recruiting - Dental Implant Clinical Trials

Management of the Fresh Extraction Socket in the Aesthetic Area

IIP/ARP/SH
Start date: September 27, 2023
Phase: N/A
Study type: Interventional

After atraumatic tooth extraction and the assessment of the feasibility of immediate implant placement, patients will be randomly assigned to one of three treatment concepts: 1. Immediate Implant Placement and Immediate Provisionalization 2. Alveolar Ridge Preservation. After 4 months of healing an implant will be placed with simultaneous GBR and/or Soft Tissue Augmentation procedures, if needed. 3. Spontaneous Healing of the socket. After 4 months of healing, an implant will be placedwith simultaneous GBR and/or Soft Tissue Augmentation procedures, if needed. In all groups, four months after implant placement, a prosthesis will be delivered. From this experimental period onward, patients will be scheduled for maintenance. Clinical, radiographic and volumetric assessment will be performed by clinicians not involved in the surgery and blind with respect to treatment assignment at 1, 3 and 5 years post loading.

NCT ID: NCT03882216 Not yet recruiting - Clinical trials for Soft Tissue Augmentation

Pontic Site Development With Connective Tissue Graft Using Modified Pouch Technique Versus Pouch Technique

Start date: June 20, 2019
Phase: N/A
Study type: Interventional

The study will be formed on two groups : the control group and the test group For both groups base line impressions will be taken before the surgery and a free gingival graft will be harvested from the palate and deepithelialized to obtain the free connective tissue graft then In the control group: the free connective tissue graft will be inserted through crestal pouch previously prepared using split thickness flap. In the test group The free connective tissue graft will be slided through apical vertical incision in the pontic area previously tunneled. Post operative casts will be obtained by taking impressions after three months and six months to evaluate the volumetric changes in the pontic area.

NCT ID: NCT03753906 Completed - Clinical trials for Soft Tissue Augmentation

Evaluation of Self-filling Osmotic Tissue Expander in Augmenting Keratinized Tissue Around Dentulous Region

Start date: November 5, 2016
Phase: N/A
Study type: Interventional

The present study is a human, prospective, single centre, single blind randomised controlled clinical tria conducted to explore the feasibility and efficacy of self-inflating hydrogel expander (Osmed®) to gain keratinised tissue around the dentulous area. The trial is in accordance to the Consolidated Standards of Reporting Trials (CONSORT) criteria, 2010.

NCT ID: NCT03425864 Completed - Clinical trials for Soft Tissue Augmentation

PES After Soft Tissue Augmentation Using CTG Around Immediate Dental Implants Versus Immediate Dental Implants Alone in Esthetic Zone

Start date: July 11, 2017
Phase: N/A
Study type: Interventional

The goal of the present study is to compare the esthetic result and stability of gingival tissue over the immediate implant only and immediate implant with connective tissue in patients with single non-restorable tooth in the esthetic zone. The main null hypothesis to be tested is that the addition of SCTG to immediately placed implants will not significantly differ from immediately placed implant alone as regard gingival tissue stability.

NCT ID: NCT03413553 Completed - Clinical trials for Soft Tissue Augmentation

Clinical Evaluation of Soft Tissue Augmentation Using CTG and PRF Around Immediately Placed Dental Implants Versus Immediate Implant Alone in Esthetic Zone .

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The main hypothesis to be certified is that the addition of Subepithelial Connective Tissue Graft (SCTG) and Platelet rich Fibrin (PRF) to immediately placed implants will not significantly differ from immediately placed implant alone as regard gingival tissue stability.

NCT ID: NCT03224442 Not yet recruiting - Clinical trials for Soft Tissue Augmentation

Soft Tissue Evaluation Around Implants Using Prf or a Palatal Pedicle

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

Clinical Evaluation of Peri-Implant Soft Tissue Around Immediately Placed Implants Using PRF Membrane Versus The Palatal Pedicle Soft Tissue Graft: A Randomized Controlled Clinical Trial.

NCT ID: NCT02864862 Completed - Dental Implant Clinical Trials

Esthetic Outcomes Following Immediate Implant Combine With Soft Tissue Augmentation

Start date: October 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the esthetic outcomes following immediate implant combined with the autogenous tissue graft or acellular dermal matrix compared to immediate implant alone.