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Mechanisms of Remote Ischaemic PreConditioning in humans

Mechanisms of Remote Ischaemic PreConditioning in humans - Me-RIPC in vitro

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37484
Enrollment
10
Registered
2012-02-23
Start date
2012-06-15
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

organprotection

Interventions

The investigational intervention is a remote ischaemic conditioning stimulus. Hereto, a pressure cuff will be placed on the upper arm and inflated to 200 mmHg for five minutes. Then, pressure will b
one baseline sample and two samples after RIPC. Each blood withdrawal will be taken by a separate venous puncture performed by a physician with extensive experience in this field, such as an anesth

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy, male volunteers aged 18-45 years.

Exclusion criteria

Exclusion criteria: Cardiovascular diseases, Alcohol or drug abuse, Fibrinolytic treatment in the previous 30 days, Usage of the anti-diabetic drug glibenclamide (this drug is known to block any conditioning effect). Doing any kind of sports on the night before the experimental day in the AMC

Design outcomes

Primary

MeasureTime frame
The primary endpoint of this study will be apoptosis, caspase 3/8/9 activity and LDH release measured at different time points in our in vitro models.

Secondary

MeasureTime frame
The secondary endpoints will be targets that will be analyzed from the Reperfusion Injury Salvage Kinase (RISK) pathway.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)