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Completed No phase listed Observational

Study of Bone Histomorphometry, Microarchitecture, and Matrix Structure in Patients Receiving Alendronate or Risedronate

ClinicalTrials.gov ID: NCT00778154

Public ClinicalTrials.gov record NCT00778154. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study of Bone Histomorphometry, Microarchitecture, and Matrix Structure in Patients Receiving Long-Term Alendronate or Risedronate

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Patients who have received the appropriate number of years of alendronate or risedronate therapy will be recruited. Each patient will have received baseline BMD measurements performed at the spine and the hip by DXA. Each patient will receive tetracycline to label the bone and then have a transiliac bone biopsy. One year later teh bone label and biopsy procedure will be repeated.

Study identification

NCT ID
NCT00778154
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Warner Chilcott
Industry
Enrollment
105 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
Not listed
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2003
Primary completion
Nov 30, 2006
Completion
Nov 30, 2006
Last update posted
Jun 4, 2013

2004 – 2006

United States locations

U.S. sites
7
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
Warner Chilcott Research Facility Palm Desert California 92269
Warner Chilcott Research Facility Lakewood Colorado 80227
Warner Chilcott Research Facility Decatur Georgia 30033
Warner Chilcott Research Facility Gainesville Georgia 30501
Warner Chilcott Research Facility Omaha Nebraska 68131
Warner Chilcott Research Facility Cincinnati Ohio 45219
Warner Chilcott Research Facility Wyomissing Pennsylvania 19610

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00778154, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 4, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00778154 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →