Skip to content

The Incidence of Gingival Fissures _ a Crossover Single-blinded Randomized Clinical Trial

The Incidence of Gingival Fissures _ a Crossover Single-blinded Randomized

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01636830
Enrollment
35
Registered
2012-07-10
Start date
2011-08-31
Completion date
2012-03-31
Last updated
2012-07-10

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

Conditions

Gingival Recession, Wounds and Injuries

Keywords

Toothbrushing, gingival recession

Brief summary

The objective of this study is to evaluate the incidence of gingival fissures according to the type of brush used, soft and medium.

Detailed description

Gingival recession constitute a functional and aesthetic problem that affects much of the population. One of the possible causes refers to a traumatic brushing. Individuals who have an excessive tooth brushing can cause injuries to your gums, such as abrasions and fissures. These lesions have been considered subrogated outcomes of gingival recession noninfectious. The literature only reports and case series showing the gingival fissures, which were once associated with traumatic occlusion. This is the first clinical trial to evaluate the gingival fissures according to the type of brush used.

Interventions

Evaluate the use of toothbrushes with bristles soft and medium

Sponsors

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul, Brazil
CollaboratorOTHER
Federal University of Rio Grande do Sul
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
14 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* good/ excellent health; * idade de 14 a 20 anos; * at least 20 teeth without a history of destructive periodontal disease, absence of gingival bleeding; * absence of loss of attachment/recession ≥2mm in molars and pre-molars in the buccal areas.

Exclusion criteria

* were unable to provide consent or comply with the sudy protocol; * smokers; * pregnant women; * persons under orthodontic treatment or with dental or implant prosthesis, presence of cervical abrasions, restorations or caries; * need of antibiotic prophylaxis associated with dental procedures.

Design outcomes

Primary

MeasureTime frameDescription
Gingival Fissures associated with toothbrushing3 monthsThis study took standardized photographs every 2 or 3 days during two periods of 28 days for evaluation of gingival fissures. These were measured by application of a disclosing solution of plaque on teeth and gums of the participants. The application developer board is safe, without contra-indications in the literature and facilitates visualization of gingival lesions and plaque.

Countries

Brazil

Outcome results

None listed

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