NCT02922010

Completed

A Follow-Up Survey of Oral Hygiene and Health Outcomes for W...

Procter and Gamble Source

Compare

Other study identifiers

Sponsor study identifier

2015108

Study Type

observational

Actual enrollment (reported)

35

Locations

1 country

Sites

1

Timeline

Study Start

June 2016

Actual (reported)

Primary Completion

June 30, 2017

Actual (reported)

Study Completion

June 30, 2017

Actual (reported)

Brief Summary

The objective of this study is to assess oral health, oral hygiene knowledge, and daily oral hygiene practices of women who participated in a randomized controlled trial (2011001) at University of Alabama Birmingham during the period 2012-2014. Additional objectives of the research include evaluation of possible cultural, biological or other mechanisms for outcomes observed in the OHMOM clinical trial, and oral health screening of children born to mothers during the study for the purposes of understanding possible multigenerational effects of oral hygiene education.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 35 participants
Study completion date: June 30, 2017
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
June 2016
Actual (reported)
First Submitted
September 29, 2016
Actual (reported)
First Posted
October 3, 2016
Actual (reported)
Primary Completion
June 30, 2017
Actual (reported)
Study Completion
June 30, 2017
Actual (reported)

Last Updated: September 19, 2017
Status Verified: September 2017
Last Update Submitted: September 18, 2017

Conditions

Gingivitis

Outcome Measures

Primary Outcomes (1)

Löe-Silness Gingivitis Index
1 Day

Eligibility Criteria

Age18 Years+

Sexfemale

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Participants from the OHMOM study and offspring from that study (NCT01549587) at the University of Alabama Birmingham.

You may qualify if:

be at least 18 years of age

Sponsors & Collaborators

Procter and Gamble
Industrylead

Study Sites (1)

Center for Women's Reproductive Health

Birmingham, Alabama, 35294-0024, United States

MeSH Terms

Conditions

Gingivitis

Condition Hierarchy (Ancestors)

InfectionsGingival DiseasesPeriodontal DiseasesMouth DiseasesStomatognathic Diseases

Study Officials

Robert W Gerlach, DDS, MPH
Procter and Gamble
STUDY DIRECTOR

Enrollment

35 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: OTHER
Time Perspective: CROSS SECTIONAL
Sponsor Type: INDUSTRY
Responsible Party: SPONSOR

Study Record Dates

First Submitted

September 29, 2016

First Posted

October 3, 2016

Study Start

June 2016

Actual (reported)

NCT06962956

Evaluating Gingivitis and Systemic Biomarkers

Phase 1Active Not Recruiting

NCT03381339

Powertoothbrushing for Treating Gingivitis

Not ApplicableCompleted

NCT02187016

Efficacy and Safety Study of Interproximal Cleaning Modalities on Oral Health

Not ApplicableCompleted

NCT02883244

Curved Soft-Picks on Plaque Accumulation on Patients With Gingivitis

Not ApplicableCompleted

NCT02750943

Potential of Stannous Fluoride Toothpaste to Reduce Gum Disease

Not ApplicableCompleted

NCT07211061

A Study is to Evaluate a Regimen on Gingivitis Using Traditional and Novel Assessment Methods

Phase 4Completed

sign an informed consent form and be given a copy

be a former subject in study 2011001 at University of Alabama Birmingham with a live birth outcome from that study.

You may not qualify if:

any medical condition requiring pre-medication prior to dental procedures
any diseases or conditions that might interfere with the subject safely completing the study
inability to undergo study procedures

Contact the study team to confirm eligibility.

Primary Completion

June 30, 2017

Actual (reported)

Study Completion

June 30, 2017

Actual (reported)

Last Updated

September 19, 2017

Record last verified: 2017-09

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT02922010
Data provider: ClinicalTrials.gov
Source updated: 2017-09-19
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:22:06 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations