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Completed Phase 4 Interventional

A Study of Ibandronate (Bonviva) in Patients With Post-Menopausal Osteoporosis

ClinicalTrials.gov ID: NCT02598440

Public ClinicalTrials.gov record NCT02598440. 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 3, 2026, 7:28 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

A Randomized, Open-Label, Muti-Center Study to Investigate Patient Preference on Dosing in Women With Postmenopausal Osteoporosis Treated With Once-Monthly Ibandronate and Once-Weekly Alendronate. A Six Month, Two-Sequence, and Two-Period Crossover Study

Brief summary

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

This study will evaluate participant-reported preference for either ibandronate or a comparator drug in women with postmenopausal osteoporosis. The anticipated time of study treatment is 6 months, and the target sample size is 338 individuals.

Study identification

NCT ID
NCT02598440
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
341 participants

Conditions and interventions

Interventions

Drug

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
Feb 29, 2004
Primary completion
Apr 30, 2005
Completion
Apr 30, 2005
Last update posted
Nov 1, 2016

2004 – 2005

United States locations

U.S. sites
54
U.S. states
29
U.S. cities
50
Facility City State ZIP Site status
Not listed Huntsville Alabama 35801
Not listed Phoenix Arizona 85006
Not listed Tempe Arizona 85282
Not listed Laguna Woods California 92653
Not listed Mission Viejo California 92691
Not listed Oceanside California 92056
Not listed San Diego California 92103-6204
Not listed San Diego California 92108
Not listed Santa Clarita California 91321
Not listed Upland California 91786
Not listed Vista California 92084
Not listed Denver Colorado 80202
Not listed Cromwell Connecticut 06416
Not listed Waterbury Connecticut 06708
Not listed Newark Delaware 19713
Not listed Aventura Florida 33180
Not listed Miami Florida 33176
Not listed Pembroke Pines Florida 33024
Not listed Tampa Florida 33614
Not listed West Palm Beach Florida 33409
Not listed Augusta Georgia 30904
Not listed Decatur Georgia 30033
Not listed Chicago Illinois 60612
Not listed Indianapolis Indiana 46202
Not listed South Bend Indiana 46601
Not listed Des Moines Iowa 50314
Not listed Wichita Kansas 67207
Not listed Bangor Maine 04401
Not listed Baltimore Maryland 21209
Not listed Worcester Massachusetts 01610
Not listed Florissant Missouri 63031
Not listed St Louis Missouri 63128
Not listed Reno Nevada 89502
Not listed Princeton New Jersey 08540
Not listed Toms River New Jersey 08753
Not listed Orchard Park New York 14127
Not listed Raleigh North Carolina 27609
Not listed Eugene Oregon 97401
Not listed Duncansville Pennsylvania 16635
Not listed Erie Pennsylvania 16502
Not listed Erie Pennsylvania 16506
Not listed Philadelphia Pennsylvania 19114
Not listed Philadelphia Pennsylvania 19148
Not listed Wyomissing Pennsylvania 19610
Not listed Warwick Rhode Island 02886
Not listed Mt. Pleasant South Carolina 29464
Not listed Nashville Tennessee 37203
Not listed Dallas Texas 75234
Not listed Houston Texas 77024
Not listed Newport News Virginia 23602
Not listed Richmond Virginia 23235
Not listed Seattle Washington 98105
Not listed Seattle Washington 98144
Not listed Madison Wisconsin 53705

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 NCT02598440, 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 Nov 1, 2016 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02598440 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →