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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00791206
Other study ID # 1000012859
Secondary ID
Status Active, not recruiting
Phase Phase 2
First received November 13, 2008
Last updated December 13, 2013
Start date November 2008
Est. completion date June 2014

Study information

Verified date December 2013
Source The Hospital for Sick Children
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

Previously, the preconditioning signaling pathways have been studied on molecular level or in animal model. By using MR spectroscopy and imaging in a dynamic human model of preconditioning, we will have a better understanding how mitochondrial and endothelial function are affected by preconditioning in-vivo.


Description:

Ischemic preconditioning is a mechanism that protects tissue against ischemia-reperfusion injury. The protective effect of preconditioning is induced by short periods (1-5 minutes) of non-lethal ischemia to the target tissue, which becomes resistant to a prolonged, otherwise lethal, period of ischemia. Despite its proven potency in experimental models, ischemic preconditioning has not reached widespread clinical application because of the difficulties in applying the stimulus to the target organ (eg Heart, Brain), and even brief ischemia to the target organ can cause dysfunction.

Remote ischemic preconditioning (RIPC) is a more clinically relevant stimulus. It has been shown that preconditioning of one coronary territory induces ischemia protection in other parts of the heart. Subsequently, other studies have shown, in rodent models, that preconditioning of one organ (eg kidney) could induce protection in other organs (eg heart). We recently have confirmed, in a series of animal and human preclinical studies, that this concept can be widened; ultimately showing that four 5-minute episodes of ischemia to the skeletal limb muscles (induced by inflating a standard blood pressure cuff to a level higher than the blood pressure) protects the heart and lungs against ischemia-reperfusion injury in children undergoing cardiac surgery using cardiopulmonary bypass.

The current research is designed to investigate with MRI spectroscopy techonology, the potential physiological mechanisms involved in the protective effects of preconditioning, and the effects of ischemia and exercise.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date June 2014
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 16 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy male and female volunteers

- Post-pubescent non-athletes between the ages of >16 and <40 years of age.

Exclusion Criteria:

- Older than 40 year old.

- Younger than 16 year old.

- Major medical condition

- Illness, surgery or medical intervention in the last 48 hours.

- Diabetes Mellitus

- Caffeine intake in the last 48 hours

- Athlete (more than 5 training sessions per week)

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


Intervention

Procedure:
Real preconditioning
Preconditioning will consist of four 5 minutes cycles of upper limb ischemia interspaced with 5 minutes of reperfusion, using a blood-pressure cuff inflated to a pressure 15 mmHg greater than systolic arterial pressure.
Sham preconditioning
Preconditioning will consist of four 5 minutes cycles of upper limb ischemia interspaced with 5 minutes of reperfusion, using a blood-pressure cuff inflated to a pressure 10mmHg with the same cycling protocol as the real preconditioning.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The Hospital for Sick Children

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in mitochondrial function following the preconditioning as evidenced by a faster rate of recovery of phosphocreatinine after exercise. 2 hours No
Primary Improvement of endothelial and microvascular dysfunction induced by 20 minutes of forearm ischemia. 1 hour No
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