Free Gingival Graft Versus Connective Tissue Graft

NCT ID: NCT05563428

Last Updated: 2022-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-01

Study Completion Date

2023-12-31

Brief Summary

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This study wil compare FGG and CTG for recession coverage in the anterior mandibula.

Detailed Description

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Conditions

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Gingival Recession Gingival Recession, Localized

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized, controlled trial
Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Free gingival graft

Free gingival graft will be conducted.

Group Type ACTIVE_COMPARATOR

Free gingival graft

Intervention Type PROCEDURE

A free gingival graft will be carried out for recession treatment.

Connective tissue graft

The recession will be treated with the pouch technique using a connective tissue graft.

Group Type ACTIVE_COMPARATOR

Connective tissue graft

Intervention Type PROCEDURE

The pouch technique with a connective tissue graft will be carried out for recession treatment.

Interventions

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Free gingival graft

A free gingival graft will be carried out for recession treatment.

Intervention Type PROCEDURE

Connective tissue graft

The pouch technique with a connective tissue graft will be carried out for recession treatment.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* ASA type I and II subjects
* Localized Gingival Recessions
* Recessions Cairo RT I-II-III
* FMPS \< 10%
* FMBS\< 10%
* \<10 cigs/ day
* No contra-indication against oral surgical interventions
* Patient is able to give inform consent

Exclusion Criteria

* Infection (local or systemic). Each infection will be evaluated prior to study procedure for suitability. Patients with gingivitis or local infection (fracture, apical reaction) will undergo a dental treatment prior to entering the study. In case of systemic infection, the evaluation will be based on medical anamneses, and if necessary will be referred to relevant medical tests.
* ASA type \> II
* Current pregnancy or breastfeeding women
* Alcoholism or chronically drug abuse
* Smokers, ≳ 10 cigarettes per day
* Immunocompromised patients
* Uncontrolled diabetes
* Untreated periodontitis
* History of previous periodontal surgery (mucogingival or other) on the teeth to be included
* Presence of severe tooth malposition, rotation or significant version of the tooth to be treated
* Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of no-compliance or unreliability
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Centre Hospitalier Universitaire de Liege

OTHER

Sponsor Role lead

Responsible Party

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Isabelle Laleman

Chef de clinique

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Szoted Gilles, MSc

Role: PRINCIPAL_INVESTIGATOR

ULiège

Locations

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CHU de Liège

Liège, , Belgium

Site Status RECRUITING

Countries

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Belgium

Central Contacts

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France Lambert, PhD

Role: CONTACT

+32 4 270 31 05

Isabelle Laleman, PhD

Role: CONTACT

Facility Contacts

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Gilles Szotek, MsC

Role: primary

Other Identifiers

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2021-242

Identifier Type: -

Identifier Source: org_study_id

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