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NCT00594334 Clinical Trial

Effect of Actonel on Periodontal Health of Postmenopausal Women

Periodontal Disease Clinical Trial

Official title:
Effect of Actonel on Periodontal Health of Postmenopausal Women

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00594334
Other study ID # 010706
Secondary ID
Status Withdrawn
Phase Phase 4
First received
Last updated
Start date January 2008
Est. completion date January 2011

Study information
Verified date July 2022
Source University Hospitals Cleveland Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hypothesis: Women who use Actonel (risedronate) for osteopenia will show beneficial periodontal effects.

Description:

Women who use Actonel for osteopenia will show beneficial attachment loss, alveolar bone height and morphology as compared to those who do not when oral hygiene is corrected for.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 2011
Est. primary completion date January 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: - Osteopenia - Postmenopausal Exclusion Criteria: - Male - Diabetes

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Risedronate
Weekly Risedronate

Locations
Country Name City State
United States Uhcmc Cleveland Ohio

Sponsors (1)
Lead Sponsor Collaborator
University Hospitals Cleveland Medical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Periodontal alveolar bone changes one year
Secondary Periodontal attachment levels one year
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