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Treatment of gengival recessions with Collagen Membrane

Treatment of Single Miller Class I Gingival Recessions With a Xenogeneic Collagen Matrix: a Split-Mouth Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6txkq3
Enrollment
Unknown
Registered
2018-01-19
Start date
2016-11-15
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Gingival Retraction

Interventions

In all, 16 patients will be selected for the study. Each of them should have 02 single gingival recessions. They will be divided into two groups. The test group will consist of 16 gingival recessions
Procedure/surgery
D003807

Sponsors

Programa de pós-graduação em odontologia da universidade federal de Pernambuco
Lead Sponsor
Programa de pós-graduação em odontologia da universidade federal de Pernambuco
Collaborator

Eligibility

Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Have 18 years of age or older. To present a single gingival recession in the buccal surface in at least two contralateral quadrants in the maxilla or mandible. Also considered are individuals who present more than one gingival retraction in the same hemiarco, but not adjacent ones. To possess Miller class I gingival recessions. Have good visible plaque control (visible plaque index <20%).

Exclusion criteria

Exclusion criteria: Present active periodontal disease. Possessing systemic disorder or being on drug therapy that interferes with healing, such as uncontrolled diabetes, blood dyskinesia, the use of steroids or high doses of anti-inflammatories. Have allergy to collagen. Smoking. Pregnancy. Teeth that present non-carious or carious cervical lesion, prosthetic crowns and prominent radicular surface.

Design outcomes

Primary

MeasureTime frame
The primary endpoint of this clinical trial will be the reduction of gingival recession in millimeters 06 months after the surgical procedure, determined though periodontal probing at the beginning and at the end of the study, in order to verify a difference of at least 2,0 mm.

Secondary

MeasureTime frame
Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactRodolfo;Rodolfo Santiago;Santiago

Programa de Pós-graduação em Odontologia da Universidade Federal de Pernambuco;Programa de Pós-graduação em Odontologia da Universidade Federal de Pernambuco

rodolfojosantiago@hotmail.com;rodolfojosantiago@hotmail.com+55 81 997666877;(81) 99766-6877

Outcome results

None listed

Source: REBEC (via WHO ICTRP)