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Ischemic preconditioning for Ischemic Preconditioning

N/A
Waitlist Available
Research Sponsored by University of Guelph
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 hours after active and control interventions (diet intervention only)
Awards & highlights

Study Summary

This trial will study the effects of two interventions on the capacity of the brachial artery to dilate during exercise. The first intervention is ischemic preconditioning, and the second is a high or low fat meal.

Eligible Conditions
  • Ischemic Preconditioning
  • Dietary Exposure

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 hours after active and control interventions (diet intervention only)
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 hours after active and control interventions (diet intervention only) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Forearm blood flow
Forearm vascular conductance
Secondary outcome measures
Blood pressure
Heart rate

Trial Design

4Treatment groups
Active Control
Placebo Group
Group I: Ischemic preconditioningActive Control1 Intervention
Group II: High fat mealActive Control2 Interventions
Group III: Ischemic preconditioning controlPlacebo Group1 Intervention
Group IV: Low fat mealPlacebo Group2 Interventions

Find a Location

Who is running the clinical trial?

University of GuelphLead Sponsor
80 Previous Clinical Trials
9,956 Total Patients Enrolled

Frequently Asked Questions

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~5 spots leftby Apr 2025