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CompletedNCT00350129Updated Mar 19, 2024

Effect of Glucose on Ocular Blood Flow

An observational study in Coronary Vasospasm, sponsored by University Hospital, Basel, Switzerland. Completed at 1 site in Switzerland. Open to participants aged 18 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-03-19.

Sponsored by University Hospital, Basel, Switzerland · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
24
Ages
18 Years to 85 Years
Sex
All
01

Study summary

The primary objective is to assess the effect of glucose on retinal vascular diameter in otherwise healthy vasospastic subjects compared to non-vasospastic controls.

The secondary objective is to compare the effect of glucose also on choroidal blood flow in otherwise healthy vasospastic subjects with non-vasospastic controls.

Read the detailed description

It is known that a glucose load can induce an increase in ocular blood flow. Acute hyperglycemia increases retinal vessel diameters in animals and humans. The purpose of this study is to compare the effect of glucose on the ocular blood flow in vasospastics and nonvasospastics. Body core temperature depends on basal metabolism. Peripheral vasoconstriction is a physiological way to preserve core temperature of the body. The etiology of primary vasospastic syndrome is unknown and potentially represents simply a reaction to a defective metabolism. Based on this hypothesis, vasospastics are expected to show a different vascular reaction to glucose.

On both study days, after an overnight fast, the subjects will be seated for 30 minutes in the Lab and local tropicamide will be applied for pupil dilatation. After stabilisation of blood pressure Retinal vessel diameter and choroidal blood flow will be assessed. Baseline blood glucose levels will be measured. Afterwards study substance (75 gram of Glucose or Aspartate) will be applied in 3 dl of water. One and a half hour later, the vascular measurements will be repeated. Ath the end of hemodynamic assessments, blood sugar level will be measured again.

02

Conditions studied

  • Coronary Vasospasm

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Keywords

  • glucose
  • vasospasm
  • RVA
  • LDF
  • vasospastic subjects
  • non-vasospastic subjects
03

In context

Coronary Vasospasm

27 studies on the registry are indexed under Coronary Vasospasm; 9 are open to participants now.

This study's enrollment of 24 is below the median of 260 across 13 observational studies indexed under Coronary Vasospasm.

Browse Coronary Vasospasm studies →

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 968 studies on the registry; 191 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

healthy vasospastic subjects, healthy non-vasospastic subjects

Inclusion criteria

  • No history of the following problems: ocular or systemic disease; chronic or current systemic or topical medication; or of drug or alcohol abuse
  • normal blood pressure (100-140 / 60-90 mmhg)
  • best corrected visual acuity above 20/25 in both eyes
  • no pathological findings upon a slit-lamp examination and indirect fundoscopy
  • ametropia within -3 to +3 diopters of spherical equivalent
  • less than 1 diopter astigmatism
  • IOP \< 20 mmHg in both eyes
  • Subjects will be classified as vasospastic if they relate a clear history of frequent cold hands (answering yes to the questions: "do you have always cold hands, even during summer time?" and "do other people tell you that you have cold hands?") and as normals if they deny such a history
  • Vasospastic propensity will also be assessed by capillaroscopy

Exclusion criteria

Exclusion Criteria:

  • Subjects describing "sometimes cold hands"
  • if the test substance cannot be ingested
  • not obtainable ocular blood flow measurements
  • abnormally high levels of glucose at any point in time
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
24 participants (actual)

Groups and cohorts

  • 1

    healthy vasospastic subjects

  • 2

    healthy non-vasospastic subjects

06

Study locations

1 site
  • University Hospital Basel, Eye Clinic
    Basel, BS 4031, Switzerland
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00350129
Lead sponsor
University Hospital, Basel, Switzerland
First posted
Jul 10, 2006
Start date
Dec 2002
Primary completion
Feb 2003
Completion
Feb 2003
Last update
Mar 19, 2024

Study contacts

Selim Orgül, MD
study director · University Hospital, Basel, Switzerland

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.

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