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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01029860
Other study ID # A3244
Secondary ID
Status Completed
Phase N/A
First received December 9, 2009
Last updated December 16, 2009
Start date March 2007
Est. completion date March 2009

Study information

Verified date March 2007
Source Aristotle University Of Thessaloniki
Contact n/a
Is FDA regulated No
Health authority Greece: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess the effect of hospital admission on 24-hour ambulatory blood pressure (ABP) in hypertensive subjects.Treated or untreated hypertensive adults with open angle glaucoma underwent in-hospital and outpatient 24-hour ABP monitoring, in random order 4 weeks apart.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date March 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria:

- age >30 years old.

- subject has signed an informed consent.

- patient has untreated ocular hypertension (IOP at 10:00 between 22-34 mm Hg)

- patient has stage 1 arterial hypertension with or without therapy

Exclusion Criteria:

- secondary hypertension.

- stage 2 or 3 hypertension, history of renal disease.

- sleep apnea.

- diabetes mellitus

- acute or chronic inflammation.

- myocardial infarction or unstable angina within the past 6 months.

- heart failure NYHA class III-IV.

- active liver disease.

- pregnancy.

- history of drug or alcohol abuse, or any other condition with poor prognosis.

- treatment with non-steroid anti-inflammatory agents, corticosteroids, beta-blockers, or any other regimen that could affect BP levels.

- smoking

Study Design

Observational Model: Case-Crossover, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Aristotle University Of Thessaloniki
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