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Collagen Matrix With and Without Enamel Matrix Derivative

Porcine Collagen Matrix With and Without Enamel Matrix Derivative for the Treatment of Gingival Recession Defects

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03467802
Enrollment
30
Registered
2018-03-16
Start date
2019-01-01
Completion date
2021-12-31
Last updated
2019-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gingival Recession

Keywords

Gingival Recession, Enamel Matrix Derivative, Porcine Collagen Matrix

Brief summary

The purpose of this prospective, double-blinded, randomized, split-mouth study is to compare the effectiveness of a porcine collagen matrix (CM) and coronally advanced flap (CAF) with or without the addition of enamel matrix derivative (EMD) in the treatment of Miller Class I, II, or predictable class III recession defects. One defect will receive CM + CAF + EMD (Experimental), while the other will receive CM + CAF (Control) alone. The treatment of 60 similarly sized Miller class I, II, or predictable class III recession defects on single-rooted teeth in 30 subjects using CM + CAF + EMD or CM + CAF alone will be evaluated. The subjects will be in good health, non-smokers, periodontally healthy with good oral hygiene and have no contraindications to periodontal surgery. Paired, similar sized defects on single-rooted teeth will be in the same subject and measure within 2mm of each other. One defect will be randomly assigned as the test group using CM + CAF + EMD, and the other as the control group using only CM + CAF. Clinical measurements will be made using a UNC-15 periodontal probe by calibrated, board certified periodontists and will include: probing depth (PD), clinical attachment level (CAL), vertical recession (RD), and width of keratinized tissue (KT). Percent root coverage (%RC) will be calculated. The measurements will be used to evaluate surgical outcome. Surgical outcome will also be assessed using stone models. All measurements will be taken at baseline (on the day of the surgery) and 3 and 6 months post-surgery for comparison.

Interventions

Enamel matrix derivative (EMD), sold under the brand name Emdogain®, is an amelogenin derivative of embryonal porcine enamel and is FDA approved for application to root surfaces to treat recession defects. Amelogenins comprise the majority of the proteins in EMD while others such as tuftelin, ameloblastin and amelin make up the remainder. EMD is thought to mimic the role of proteins crucial to cementogenesis and root development, which may promote new gingival attachment to exposed roots. The properties of EMD may favor early healing of the soft tissue and stimulate angiogenesis.

DEVICEPorcine collagen matrix

Mucograft® is a bi-layered grafting material composed of Type I and III collagen. It is derived from veterinary certified pigs, sterilized by gamma irradiation and has a low antigenicity in conjunction with good biocompatibility. The material is approximately 2.5-5mm thick and is indicated for root coverage, increasing keratinized tissue, covering of implants placed immediately and alveolar ridge reconstruction. A compact outer layer contributes to protection, structure and allows for better control during suturing; while the inner layer is thick, porous and spongy in nature, providing a suitable environment for early vascularization and promotion of cellular in-growth.

Sponsors

Walter Reed National Military Medical Center
Lead SponsorFED

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age 18 years or over * Patient will remain in the Capital region for at least 6 months following the surgical procedure for follow up appointments * Patient must be otherwise periodontally healthy * Patient must be systemically healthy (ASA class I or II) * Patient must have no contraindications to periodontal surgery * Patient must have demonstrated good oral hygiene (plaque index \<1 according to Silness and Löe) * Paired Miller Class I, II or predictable III recession defects * Bilateral, facial defects on single-rooted teeth

Exclusion criteria

* Self-reported history of smoking within previous 6 months * Does not meet any of the preceding criteria * Female patients who are pregnant or nursing * Antibiotic medications taken within the last 6 months * History of mucogingival surgery at the sites of interest * Poor plaque control (\>25% of sites) * Those with clinically significant systemic disease, which may affect healing (i.e. uncontrolled diabetes or bone metabolic disease) * Allergy to chlorhexidine gluconate (Peridex) * Does not sign study consent or HIPAA forms * Bleeding complications (e.g. hemophilia) * Warfarin therapy * History of osteoporosis or taking bisphosphonate medications * History of radiation therapy in the head and neck area * Mobile teeth beyond physiologic mobility * Facial restorations at the site to be treated * Recession defects that will require more than one 15x20mm Mucograft (per side)

Design outcomes

Primary

MeasureTime frameDescription
Change in gingival recession using conventional measurementsBaseline to 6 monthsChange in gingival recession measurements from baseline to 6 months
Change in root coverage using digital analysisBaseline to 6 monthsAssessment of surgical outcome by optically scanning stone models captured at baseline to 6 months post-surgery. The digital files will be aligned using global registration and GR recorded by measuring the distance from cemento-enamel junction to the height of the marginal gingiva using computer software. % RC will be calculated by comparing GR at the various times.
Change in Probing DepthsBaseline to 6 monthsChange in Probing Depthmeasurements from baseline to 6 months
Change in Clinical Attachment LevelsBaseline to 6 monthsChange in Clinical Attachment Levels measurements from baseline to 6 months
Change in Keratinized TissueBaseline to 6 monthsChange in Keratinized Tissue measurements from baseline to 6 months

Secondary

MeasureTime frameDescription
Comparison of digital vs. conventional measurementBaseline to 6 monthsCompare conventional and digital change in gingival recession to assess the two modalities treatment outcomes

Countries

United States

Contacts

Primary ContactRyan A Kaye, DMD
ryan.a.kaye.mil@mail.mil3012952127
Backup ContactBrent Tibbet, DMD
3013194831

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026