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⚡ Current Task Assignment
🧬 Genetic Analysis
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📊 Resource Allocation by Research Phase:
📚 Data Analysis
🧪 Experimental Design
🔬 Clinical Trials
💊 Treatment Development
Two year study to determine the safety and efficacy of weekly 35 mg Risedro...
Status
Completed
Location
Research Site
Start Date
2002-06
Trial ID
NCT00619957
Treatments Being Tested
The effects of stopping long-term (7 years) and short term (2 years) risedr...
Status
Completed
Location
Investigational Site
Start Date
2001-10
Trial ID
NCT01249261
Treatments Being Tested
Investigators are building an empirical evidence base for real world data t...
Status
Completed
Location
Brigham and Women's Hospital
Start Date
2020-10-29
Trial ID
NCT04879420
Treatments Being Tested
This is a 2year observational study that will recruit patients who have pre...
Status
Completed
Location
Sheffield Teaching Hospitals NHS Foundation Trust
Start Date
2010-03
Trial ID
NCT01406613
Treatments Being Tested
Compare subject satisfaction of once a week dosing of 35 mg Risedronate to ...
Status
Completed
Location
Sanofi-Aventis
Start Date
2003-10
Trial ID
NCT00549965
Treatments Being Tested
The primary objective of this pilot study is to estimate the percent change...
Status
Completed
Location
Multiple Locations
Start Date
2002-11
Trial ID
NCT00351091
Treatments Being Tested
Femoral neck fracture in the elderly is one indication for initiating osteo...
Status
Unknown
Location
Siriraj Hospital
Start Date
2013-06
Trial ID
NCT02148848
Treatments Being Tested
To evaluate the effect of subject knowledge of their disease status on pers...
Status
Completed
Location
Sanofi-Aventis
Start Date
2002-07
Trial ID
NCT00616694
Treatments Being Tested
The occurrence of bone loss in Crohn's disease patients is an important cli...
Status
Completed
Location
Gastrointestinal and Liver Disease Research (GILDR) Group
Start Date
TBD
Trial ID
NCT01215890
Treatments Being Tested
The primary purpose of participation in this study is to answer whether ter...
Status
Completed
Location
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Start Date
2012-10
Trial ID
NCT01709110
Treatments Being Tested