Clinical Trial Results:
INFLUENCE OF NEBIVOLOL ON OCULAR PERFUSION IN PATIENTS WITH ARTERIAL HYPERTENSION AND GLAUCOMA
A mono-center, active-substance controlled, randomized, double-blind,
prospective phase IV parallel-group trial comparing Nebivolol with Bisoprolol
Summary
|
|
EudraCT number |
2004-004862-33 |
Trial protocol |
DE |
Global completion date |
23 Jan 2008
|
Paediatric regulatory details
|
|
Is the trial part of an agreed EMA paediatric investigation plan? |
No
|
Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? |
No
|
Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? |
No
|
Results information
|
|
Results version number |
v1(current) |
This version publication date |
30 Mar 2016
|
First version publication date |
30 Mar 2016
|
Other versions |
|
Summary report(s) |
Synopsis of CSR |
Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to Commission Guideline 2012/C 302/03
for further information.