An Open Clinical Trial to Assess the Influence of Newly Prescribed Aminobiphosphonates on Arterial Stiffness
Sponsor
Technische Universität Dresden (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00180232
Collaborator
(none)
0
1
2
0
Study Details
Study Description
Brief Summary
The study tries to reveal if aminobisphosphonates influence aside the bone density also the vascular status in the typical elderly patient population
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
|
Detailed Description
The subjects - starting bisphosphonate treatment due to medical reasons - will be additionally investigated as outpatients (arterial stiffness, applanation tonometry), for each subject 3 individual dates with a duration of approx. 30 min each are scheduled, prior to therapy with bisphosphonate, after 3 and 6 month of treatment
Study Design
Study Type:
Observational
Actual Enrollment
:
0 participants
Time Perspective:
Prospective
Official Title:
An Open Clinical Trial to Assess the Influence of Newly Prescribed Aminobiphosphonates on Arterial Stiffness (Changes of the Aortal Elasticity Due to a Newly Established Aminobiphosphinate Therapy for the Treatment of Osteoporosis)
Study Start Date
:
Apr 1, 2006
Actual Study Completion Date
:
Jun 1, 2006
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| 1 Patients starting an aminobisphosphonate therapy due to medical reasons Broca-index: between -20 and +25% who are willing and capable to confirm written consent to enrolment after ample information has been provided |
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- Patients starting an aminobisphosphonate therapy due to medical reasons Broca-index: between -20 and +25% who are willing and capable to confirm written consent to enrolment after ample information has been provided
Exclusion Criteria:
- patients with major cardiovascular disease patients participating in another clinical trial 1month prior to inclusion in this study patients unable or unwilling to give informed consent
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Medizinische Fakultät der Technischen Universität Dresden | Dresden | Germany | 01307 |
Sponsors and Collaborators
- Technische Universität Dresden
Investigators
- Principal Investigator: Joachim Siegert, MDDPharm,Phd, Technische Universität Dresden
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00180232
Other Study ID Numbers:
- EK160082004
First Posted:
Sep 16, 2005
Last Update Posted:
Feb 3, 2012
Last Verified:
Feb 1, 2012