Recession, Gingival Clinical Trial
Official title:
Tunnel Versus Coronally Advanced Flap Combined With a Connective Tissue Graft for the Treatment of Gingival Recessions: Long Term (4 Years) Follow-up of a Randomized Controlled Trial
NCT number | NCT04016493 |
Other study ID # | H2011-1 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 2013 |
Est. completion date | January 2019 |
Verified date | July 2019 |
Source | University of Liege |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Few studies evaluate the outcomes beyond 1 year follow up for gingival recessions treatments using the tunnel technique in combination with connective tissue graft. The aim of this randomized controlled trial (RCT) was to compare the 4-year outcomes of the CAF versus the pouch/tunnel (TUN) technique both associated with CTG.
Status | Completed |
Enrollment | 40 |
Est. completion date | January 2019 |
Est. primary completion date | January 2014 |
Accepts healthy volunteers | |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Miller's class I recessions; - Recession of 2 mm to 5 mm; - Maxillary incisors, canines or premolars; - Identifiable cementoenamel junction (CEJ); - Patients minimum 18 years old; - No/controlled periodontal disease; - ASA1 or ASA2 (American Society of Anesthesiologists) general health status; - Providing a signed informed consent form. Exclusion criteria were: - Smokers; - Presence of cervical carious lesion; - Pocket depth greater than 4 mm; - Sites where previous muco-gingival therapy was performed; - Pregnancy. - In presence of non-carious cervical lesions, the anatomical CEJ was reconstructed by the use of a composite before the procedure. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Liege |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Plaque Index Change | The plaque accumulation is assessed at baseline, 6 months and 4 years follow-up visits using a 0-1 scoring system, 0 being the the highest value, 1 being the lowest result (0 =No detectible plaque ; 1 = Plaque can be seen by the naked eye) | baseline, 6 months and 4 years | |
Primary | Bleeding on probing score change | The bleeding tendency is assessed at baseline, 6 months and 4 years follow-up visits as : 0 No bleeding when a periodontal probe is passed along the gingival margin adjacent to the implant; 1 Isolated bleeding spots visible ; 2 Blood forms a confluent red line on the margin; 3 Heavy or profuse bleeding. | baseline, 6 months and 4 years | |
Primary | Recession width change | The status of the recession width was recorded at baseline, 6 months and 4 years follow-up visits. The scale is in mm. More large is it, worst it is Minest large it is, best it is |
baseline, 6 months and 4 years | |
Primary | Gingival thickness change | The gingival thickness was recorded at baseline, 6 months and 4 years follow-up visits. The scale is in mm. More thick is it, best it is Minest thick it is, worst it is |
baseline, 6 months and 4 years | |
Primary | Keratinised mucosa height change | The status of the keratinised mucosa height was recorded at baseline, 6 months and 4 years follow-up visits. The scale is in mm. More large is it, best it is Minest large it is, worst it is |
baseline, 6 months and 4 years | |
Primary | Mean Root Coverage change | The status of the Mean Root Coverage was recorded at 6 months and 4 years follow-up visits. The scale is in mm. More long it is, best it is Minest long it is, worst it is |
at 6 months and 4 years. | |
Primary | PES Assessment change | The PES was assessed according to the seven parameters described by Fürhauser (Fürhauser et al., 2005). | Baseline, 6 months and 4 years | |
Secondary | Patient-related esthetic outcomes | (Fürhauser et al., 2005). Patient-related esthetic outcomes were also recorded in a questionnaire using a 0-14 graduated scale (0 being the worst and 14 the best value). | 4 years |
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