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Compares treatment options for Defect in Alveolar Ridge
Official title Novel Technique Versus Conventional Subepithelial Connective Tissue Graft in Treatment of Ridge Contour Defects
ClinicalTrials.gov ID: NCT06435780
What this study is testing
- What it's testing
- The aim of the study is to clinically and radiographically evaluate and compare two techniques to augment soft tissues: the conventional subepithelial connective tissue graft technique and a novel denuded interpositional pedicled rolled flap technique (DIPRF) These techniques will be used to augment edentulous ridges that are recommended for rehabilitation by an implant or a fixed restoration.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 50
You may be able to join if
- Adults above the age of 18 to 50 years.
- Males and females as confirmed by asking the female patients about whether they are pregnant or not
- Patient's with Seibert classification class I requiring future rehabilitation of one or more premolar region and sound adjacent teeth.
- Soft tissue thickness on the palatal tissues more than 6mm at the site of harvesting the graft.
- Presence of Mandibular posterior teeth opposing the tooth to be replaced for occlusion.
You likely can't join if
- Patients with ridge defects due to bone defect
- Smoker patients who smoke more than 10 cigarettes per day
- Pregnant females
See the full eligibility criteria
- Adults above the age of 18 to 50 years.
- Males and females as confirmed by asking the female patients about whether they are pregnant or not
- Patient's with Seibert classification class I requiring future rehabilitation of one or more premolar region and sound adjacent teeth.
- Soft tissue thickness on the palatal tissues more than 6mm at the site of harvesting the graft.
- Presence of Mandibular posterior teeth opposing the tooth to be replaced for occlusion.
- Clinically healthy soft tissues with no signs of clinical pathology of the soft tissue.
- Good oral hygiene.
- Patient accepts to sign an informed consent.
- ASA I or ASA II Patient.
- Patients with ridge defects due to bone defect
- Smoker patients who smoke more than 10 cigarettes per day
- Pregnant females
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 50 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.