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Comparison Between Two Coronally Positioned Flap With Connective Tissue

Comparison of Two Bilaminar Techniques for Root Covering of Miller´s Recessions Class I and II: A Blind, Randomized Controlled Clinical Trial

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01814592
Enrollment
72
Registered
2013-03-20
Start date
2013-03-31
Completion date
2014-08-31
Last updated
2013-03-26

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

Conditions

Gingival Recession, Periodontal Atrophy

Keywords

coronally positioned flap, connective tissue, gingival margin, gingival recession/ treatment, gingival recession/ surgery, subepithelial connective tissue graft, randomized controlled clinical trial, surgical flaps, Treatment outcome

Brief summary

The aim of this study is to evaluate the effectiveness of total root coverage between two coronally positioned flap technique in Miller recession Class I and II, in patients attending at Universidad El Bosque dental school clinics.

Detailed description

This is a blind, randomized controlled clinical trial.

Interventions

PROCEDUREcoronally partial thickness flap plus connective tissue

The design of the flap will be performed according to the technique described by de Sanctis and Zucchelli 2007.

PROCEDUREcoronally mucosal thickness flap

The design of the flap will be performed according to the technique described by Greenwell H, Vance G, Munninger B and Johnston H.

Sponsors

Universidad El Bosque, Bogotá
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Class I and II Miller recessions showing a recession depth ≥ 2 mm. * Recessions isolated and / or maximum continuous two teeth. * Recessions in incisors, canines and premolars * Patients 20 to 60 years old.

Exclusion criteria

* Systemic compromise, that contraindicates any periodontal surgical procedure. * Warfarin medication. * Uncontrolled diabetes mellitus with glycosylated hemoglobin ≥ 8 * Chronic steroid therapy (dose of 7.5 mg/ day for more than 14 days) * HIV-AIDS infection with CD4 counts \<200. * Immunosuppression. * Recessions molars not be taken into account in the study. * Patients who have used antibiotics one month prior to the surgical procedure. * Pregnancy. * Active smoker. * Patients with a history of periodontal surgery at the recession area that has taken place in the last three months. * Severe dental malposition, teeth rotation, versions teeth root coverage that contraindicates surgery. * Non carious cervical lesions or caries where is not visible the cemento- enamel junction (CEJ). * Active inflammation that contraindicates surgical procedure of the recession. * Active Orthodontics

Design outcomes

Primary

MeasureTime frame
Assess percentage of total root coverage between two subepithelial conective tissue graft technique for covering Class I and II Miller recessions patients attending at dental clinics of Universidad El Bosqueone month (plus or minus 2 days), three months (plus or minus 3 days) and six months (plus or minus 5 days)

Secondary

MeasureTime frame
Assess the proportion of root coverageone month (plus or minus 2 days), Three months (plus or minus 3 days) and six month (plus or minus 5 days)
Clinical attachment level, width of keratinized tissue and the position of the mucogingival junction following root coverage proceduresone month (plus or minus 2 days), three months (plus or minus 3 days) and six months (plus or minus 5 days)

Other

MeasureTime frame
Assess the frequency of adverse events0 hours (intrasurgical), 1-24 hours (immediate postoperative), 25 hours to 6 days (mediate postoperative) and 7 or more days (late postoperative)

Countries

Colombia

Outcome results

None listed

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