Role of Endothelin- and Nitric Oxide-system in the Regulation of Optic Nerve Head Blood Flow During Changes in Ocular Perfusion Pressure

Sponsor
Medical University of Vienna (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00406731
Collaborator
(none)
0
1
82
0

Study Details

Study Description

Brief Summary

Autoregulation is the ability of a vascular bed to maintain blood flow despite changes in perfusion pressure. The existence of an effective autoregulation in the optic nerve circulation has been shown in animals and humans. The exact mechanism behind this autoregulation is still unknown. The motive for the investigation of optic nerve head (ONH) blood flow autoregulation is to enhance the understanding of pathologic eye conditions associated with ocular vascular disorders. To clarify the regulatory mechanisms of ONH microcirculation is of critical importance to understand the pathophysiology of glaucoma because there is evidence that glaucoma is associated with optic nerve head ischemia. Several studies indicate that a disturbed autoregulation might contribute to glaucomatous optic neuropathy. Previous findings suggest endothelial dysfunction in glaucomatous optic neuropathy, in particular alterations in endothelin- and nitric oxide- system, which both play an important role in local regulation of vascular tone.

In the present study, changes in ocular perfusion pressure will be performed during administration of drugs, which may potentially alter the pressure-flow relationship. These drugs include endothelin-1 and the nitric oxide synthase inhibitor NG-monomethyl-L-arginine (L-NMMA).

Condition or Disease Intervention/Treatment Phase
  • Drug: NG-monomethyl-L-arginine (L-NMMA)
  • Drug: Endothelin-1 (ET-1)
  • Drug: Physiologic saline solution (placebo control)
  • Device: Laser Doppler flowmetry
  • Device: Goldmann applanation tonometer
  • Device: HP-CMS patient monitor
  • Procedure: Suction cup method
Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Role of endothelin-and Nitric Oxide-system in the Regulation of Optic Nerve Head Blood Flow During Changes in Ocular Perfusion Pressure
Study Start Date :
Jan 1, 2008
Actual Primary Completion Date :
Nov 1, 2014
Actual Study Completion Date :
Nov 1, 2014

Outcome Measures

Primary Outcome Measures

  1. ONH pressure-flow relationship [up to 3 study days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Men aged between 18 and 35 years, nonsmokers

  • Body mass index between 15th and 85th percentile (Must et al. 1991)

  • Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant

  • Normal laboratory values unless the investigator considers an abnormality to be clinically irrelevant

  • Normal ophthalmic findings, ametropy < 1 Dpt

Exclusion Criteria:
  • Regular use of medication, abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study

  • Treatment in the previous 3 weeks with any drug

  • Symptoms of a clinically relevant illness in the 3 weeks before the first study day

  • History of hypersensitivity to the trial drug or to drugs with a similar chemical structure

  • History or presence of systemic or pulmonary hypertension, or other cardiac or pulmonary diseases

  • History or presence of gastrointestinal, liver or kidney disease, or other conditions known to interfere with, distribution, metabolism or excretion of study drugs

  • Blood donation during the previous 3 weeks

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Clinical Pharmacology, Medical University of Vienna Vienna Austria 1090

Sponsors and Collaborators

  • Medical University of Vienna

Investigators

  • Principal Investigator: Gabriele Fuchsjaeger-Mayrl, MD,Univ.Doz., Department of Clinical Pharmacology, Medical University of Vienna

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gerhard Garhofer, Assoc. Prof. PD Dr., Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT00406731
Other Study ID Numbers:
  • OPHT-080206
First Posted:
Dec 4, 2006
Last Update Posted:
Aug 15, 2019
Last Verified:
Aug 1, 2019
Keywords provided by Gerhard Garhofer, Assoc. Prof. PD Dr., Medical University of Vienna
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 15, 2019