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Completed Phase 4 Interventional Results available

A Study Comparing Monthly Boniva (Ibandronate) and Weekly Risedronate in Women With Post-Menopausal Osteoporosis.

ClinicalTrials.gov ID: NCT00377234

Public ClinicalTrials.gov record NCT00377234. 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 4, 2026, 2:29 AM EDT

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

Official title

Randomized, Open-label, Multi-center Study to Investigate Patient Preference on Dosing in Women With Postmenopausal Osteoporosis Treated With Once Monthly Ibandronate and Once Weekly Risedronate. A Six Month, Two-sequence and Two-period Crossover Study.

Brief summary

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

This 2 arm crossover study will evaluate patient reported preference for either once monthly Boniva (150mg p.o.) or once weekly risedronate (35mg p.o.). Patients with post-menopausal osteoporosis will be randomized to receive Boniva for 3 calendar months or risedronate for 12 weeks; they will then cross over to receive the alternative treatment for a further 12 weeks/3 months. The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals.

Study identification

NCT ID
NCT00377234
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
356 participants

Conditions and interventions

Eligibility (public fields only)

Age range
55 Years to 80 Years
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
Apr 30, 2006
Primary completion
Jul 31, 2008
Completion
Jul 31, 2008
Last update posted
Jul 31, 2016

2006 – 2008

United States locations

U.S. sites
48
U.S. states
21
U.S. cities
45
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294-3708
Not listed Mesa Arizona 85213
Not listed Scottsdale Arizona 85251
Not listed Jonesboro Arkansas 72401
Not listed Anaheim California 92801
Not listed San Diego California 92108
Not listed Waterbury Connecticut 06708
Not listed Boynton Beach Florida 33437
Not listed Jupiter Florida 33458
Not listed Largo Florida 33777
Not listed Leesburg Florida 34748
Not listed Merritt Island Florida 32952
Not listed Ocala Florida 34471
Not listed Pembroke Pines Florida 33024
Not listed Spring Hill Florida 34667
Not listed St. Petersburg Florida 33606
Not listed Tampa Florida 33614
Not listed West Palm Beach Florida 33409
Not listed Douglasville Georgia 30134
Not listed Gainesville Georgia 30501
Not listed Marietta Georgia 30060
Not listed Madisonville Kentucky 42431
Not listed Bethesda Maryland 20817
Not listed Missoula Montana 59801
Not listed Omaha Nebraska 68134
Not listed Morehead City North Carolina 28557
Not listed New Bern North Carolina 28562
Not listed Jamestown North Dakota 58401
Not listed Cincinnati Ohio 45224
Not listed Cincinnati Ohio 45236
Not listed Mogadore Ohio 44260
Not listed Tulsa Oklahoma 74104
Not listed Duncansville Pennsylvania 16635
Not listed Erie Pennsylvania 16506
Not listed Feasterville Pennsylvania 19053
Not listed Philadelphia Pennsylvania 19114
Not listed Anderson South Carolina 29621
Not listed Memphis Tennessee 38120
Not listed Selmer Tennessee 38375
Not listed Bedford Texas 76021
Not listed Bryan Texas 77802
Not listed Dallas Texas 75231
Not listed Houston Texas 77024
Not listed Houston Texas 77030
Not listed Temple Texas 76502
Not listed Richmond Virginia 23235
Not listed Richmond Virginia 23294
Not listed Seattle Washington 98105

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00377234, 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 Jul 31, 2016 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00377234 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →