Clinical Trials Directory

Trials / Completed

CompletedNCT06753084

Keratinized Tissue Augmentation Using Porcine Collagen Matrix (Mucoderm®) Around Dental Implant

Keratinized Tissue Augmentation Using Porcine Collagen Matrix (Mucoderm®) Around Dental Implant: A Randomized Clinical Study

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
22 (actual)
Sponsor
ahmed amer · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Aim of the Study To evaluate the using of porcine collagen matrix for keratinized tissue augmentation around delayed dental implant. Primary Outcome: Peri-implant keratinized mucosal width and thickness following the use of porcine collagen matrix using (Mucoderm®-Botiss gmbh) compared to the gold standard FGG augmentation. Secondary Outcome: 1. Crestal bone change (CBC) 2. Pocket depth (PD) 3. Bleeding on probing (BOP) 4. Plaque index (PI) PICOT P: Population: Patient with suitable ridge dimension for delayed implant placement. I: Intervention: Implant insertion followed by porcine collagen matrix soft tissue augmentation C: Control: Autogenous FGG O: Outcomes * Enhancing keratinized mucosal width and thickness * Evaluating : 1. Crestal bone change (CBC) 2. perimplant Pocket depth (PD) 3. Bleeding on probing (BOP) 4. Plaque index (PI) 5. Modified PES. T: Time A 6 months follow up .

Detailed description

this study aiming to augment KMW with FGG and MUCODERM following apically positioned flap the primary outcomes to measure is KMW and MT

Conditions

Interventions

TypeNameDescription
PROCEDUREAllodermthe study is done to patient who lacks of keratinized mucosa width by apically positioned flap and using of FGG as gold standard and Mucoderm as compartive group

Timeline

Start date
2023-11-01
Primary completion
2024-07-01
Completion
2024-07-25
First posted
2024-12-31
Last updated
2024-12-31

Locations

2 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06753084. Inclusion in this directory is not an endorsement.