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Role of Nitric Oxide in Optic Nerve Head Blood Flow Regulation During Isometric Exercise in Healthy Humans

Medical University of Vienna logo

Medical University of Vienna

Status

Completed

Conditions

Healthy

Treatments

Device: Goldmann applanation tonometer
Drug: Phenylephrine
Other: squatting
Drug: Physiological saline solution (as placebo)
Device: Laser Doppler Flowmetry
Drug: NG-monomethyl-L-arginine (L-NMMA)

Study type

Interventional

Funder types

Other

Identifiers

NCT00806741
OPHT-300708

Details and patient eligibility

About

Autoregulation is defined as the ability of a vascular bed to adapt its vascular resistance to changes in perfusion pressure. In the eye, several studies have reported that retinal blood flow is autoregulated over a wide range of ocular perfusion pressures. The investigators recently showed that nitric oxide (NO) is a key metabolite in the regulation of vascular tone in the eye and plays an important role in the blood flow autoregulation of the choroidal circulation. However, no data is yet available for the optic nerve head. Thus, the present study is designed to test the hypothesis that NO plays also a role in optic nerve head blood flow autoregulation. Therefore, subjects will perform squatting to increase systemic perfusion pressure during administration of either a nitric oxide synthase inhibitor (L-NMMA), an α-receptor agonist (phenylephrine) or placebo. Optic nerve head blood flow will be continuously measured during the procedure to investigate optic nerve head autoregulation.

Enrollment

18 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men and women aged between 18 and 35 years, nonsmokers
  • Men and women will be included in equal parts
  • Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant
  • Normal findings in the laboratory testings unless the investigator considers an abnormality to be clinically irrelevant
  • Normal ophthalmic findings, ametropia less than 3 diopters

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 (except intake of oral contraceptives)
  • Symptoms of a clinically relevant illness in the 3 weeks before the first study day
  • 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
  • Pregnancy

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

18 participants in 3 patient groups, including a placebo group

1
Active Comparator group
Description:
NG-monomethyl-L-arginine (L-NMMA)
Treatment:
Device: Laser Doppler Flowmetry
Other: squatting
Drug: NG-monomethyl-L-arginine (L-NMMA)
Device: Goldmann applanation tonometer
2
Active Comparator group
Description:
Phenylephrine
Treatment:
Device: Laser Doppler Flowmetry
Other: squatting
Drug: Phenylephrine
Device: Goldmann applanation tonometer
3
Placebo Comparator group
Description:
Physiological saline solution
Treatment:
Device: Laser Doppler Flowmetry
Other: squatting
Drug: Physiological saline solution (as placebo)
Device: Goldmann applanation tonometer

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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