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Effect of Non-surgical Periodontal Treatment

Effect of Non-surgical Periodontal Treatment on Pregnant Women With Periodontitis: a Randomized Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01533792
Acronym
EONSPT
Enrollment
40
Registered
2012-02-15
Start date
2010-03-31
Completion date
2010-12-31
Last updated
2012-02-17

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

Conditions

Adverse Effects, Periodontal Diseases

Keywords

Treatment, pregnant women, periodontitis, dental scaling, dental plaque

Brief summary

Objective: The objective of this research was to compare the effect of a single session supragingival scaling in a group of pregnant women with periodontal disease with a group that received supra and subgingival scaling. Methods: The investigators included 34 pregnant women between 15 and 43 who had at least 4 teeth with probing depth ≥ 4 mm or clinical attachment loss ≥ 3 mm, with bleeding on probing in the same place. Women were divided into two groups, the group 1 received supra and subgingival scaling associated with oral hygiene orientation (OHO) and the group 2 received only supragingival scaling with OHO too.

Interventions

PROCEDURESupra/subgingival scaling using periodontal curette scraping

The experimental group received supra and subgingival therapy with periodontal curettes

PROCEDURESupra and subgingival scaling

The experimental group received supra and subgingival scaling.

Sponsors

Universidade Federal do Maranhão
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 43 Years
Healthy volunteers
No

Inclusion criteria

* Pregnant women between 15 and 43 who had at least 4 teeth with probing depth ≥ 4 mm or clinical attachment loss ≥ 3 mm, with bleeding on probing in the same place.

Exclusion criteria

* Patients with systemic disease or who used medications that interfere in the etiological factors of periodontal disease in the last six months, who wore braces and / or prosthetic devices, and women smokers who did not complete treatment.

Design outcomes

Primary

MeasureTime frameDescription
Effect of non-surgical periodontal treatment in pregnancy with periodontal disease30 daysA single calibrated examiner performed clinical examination in pregnant women participating in the measurement of parameters: probing depth, clinical attachment level, hyperplasia, recession, bleeding, presence of plaque and tooth mobility on a standardized form. Quantitative parameters were evaluated at six sites per tooth: mesio/medium/ distobuccal and mesio/medium/distolingual through millimeter periodontal probe-type Williams. The bleeding and the presence of plaque in dichotomous variables were measured: present and absent. All patients received oral hygiene orientation (OHO).
Effect of non-surgical periodontal treatment in pregnancy with periodontitisAssess periodontal disease at times: initial (when pregnancy arrived) and final (30 days after periodontal therapy).The patients were randomly divided by lottery into two groups. The group 1, termed SUPRA/SUB received OHO, supra and subgingival scraping and the group 2: SUPRA supragingival scraping and OHO. In both groups, the scaling procedure was performed using periodontal curettes type Mc Call 13-14 and 17-18 (DUFLEX) in one session. Within 30 days after the initial session scraping clinical parameters were reevaluated, and now, according to every need, the patients were submitted to the supra and subgingival therapy. Noting that full dental care was provided to participants.

Outcome results

None listed

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