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Evaluations of the effect of smoke in the periodontal surgery technique using a microscope for treatment of root exposure caused by gingival recession

Evaluations the periodontal microsurgery technique for treatment of gingival recession on smokers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2w97k4
Enrollment
Unknown
Registered
2018-08-28
Start date
2010-08-01
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 recession

Interventions

Experimental group: 12 smokers with a history of smoking for at least 5 years, with an average daily intake of 10 or more cigarettes per day
with Miller's class II gingival recession, greater than or equal to 2 mm, located in the canine or premolars. Control group: 14 individuals who reported never smoked
with Miller's class II gingival recession, greater than or equal to 2 mm, located in the canine or premolars. The gingival recessions of the test (smoking) and control groups (nonsmokers) were treated
Procedure/surgery
E04.494
Q65.070

Sponsors

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Lead Sponsor
Fundação de Amparo à Pesquisa do estado da Bahia (FAPESB)
Collaborator

Eligibility

Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients smokers and nonsmokers with Miller Class I and II buccal gingival recessions equal ou greater then 2.0 mm located in maxillary canines or premolars; probing depth (PD) smaller then 3 mm without probing bleeding; absence of cavities, restorations , pulp alterations and orthodontic appliances in the areas to be treated; good general health; absence of contraindications to the surgical procedure; did not use medications that could interfere with the health of periodontal tissue or healing. Smokers should report a minimum consumption of 10 cigarettes per day for at least 5 years.

Exclusion criteria

Exclusion criteria: Smokers with daily consumption of tobacco less than 10 cigarettes per day for at least 5 years.

Design outcomes

Primary

MeasureTime frame
Root coverage percentage calculated after 6 months of postoperative follow-up according to the following formula: 100- (Recession height at the end) X 100 / (Recession height at the beginning); The measurement was performed with the use of a digital caliper

Secondary

MeasureTime frame
Clinical attachment level measured in millimeters 28 days after initial preparation and 6 months after root covering surgery; Measurement performed using a millimeter periodontal probe ;Depth of probing measured in millimeters 28 days after the initial preparation and 6 months after the radicular covering surgery; Measurement performed using a millimeter periodontal probe ;Gingival recession height measured in millimeters 28 days after initial preparation and 6 months after root rcovering surgery; Measurement performed with the use of a digital caliper ;Gingival recession width measured in millimeters 28 days after initial preparation and 6 months after root covering surgery; Measurement performed with the use of a digital caliper ;Keratinized mucosal height measured in millimeters 28 days after the initial preparation and 6 months after the radicular covering surgery; Measurement performed with the use of a digital caliper after pigmentation of the mucogingival line with Schiller's solution ;Keratinized mucosal thickness measured in millimeters 28 days after the initial preparation and 6 months after the radicular covering surgery; Measurement performed using an endodontic duster and rubber stop;The set was inserted into the gingiva 2mm apical to the gingival margin, until the buccal bone plate, when the rubber stop was positioned making slight contact with the gingiva; The distance between the tip os the endodôntico duster and the rubber stop was then measured using the digital caliper ;Complete root coverage percentage was obtained from the percentage of cases with 100% of root coverage (no root exposure) ;Satisfaction with aesthetic result assessed from a questionnaire delivered to the patients at the end of the study (6 months after surgery) ;Postoperative morbidity assessed from a pain scale delivered to patients at the end of surgery; They were instructed to note, if they needed to use analgesic medication for postoperative pain, the time of

Countries

Brazil

Contacts

Public ContactRenata Barbosa

Escola Bahiana de Medicina e Saúde Pública

renataab@yahoo.com.br+55-071-99966-2889

Outcome results

None listed

Source: REBEC (via WHO ICTRP)