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Effects of Sevoflurane in Subanesthetic Concentrations on the Forearm Perfusion

University of Zurich (UZH) logo

University of Zurich (UZH)

Status and phase

Unknown
Phase 4

Conditions

Ischemia/Reperfusion Injury

Treatments

Drug: Sevoflurane (Preconditioning)

Study type

Interventional

Funder types

Other

Identifiers

NCT00526695
17-2005

Details and patient eligibility

About

Sevoflurane preconditioning and cardiovascular protection against ischemia/reperfusion injury.

Study hypothesis: The volatile anesthetic sevoflurane at subanesthetic concentrations achieves endothelial protection against ischemia/reperfusion injury and reduces inflammatory markers in the circulation

Full description

Healthy volunteers are included in the study to investigate endothelial function and platelet activation after preconditioning by sevoflurane in subanesthetic concentrations.

Forearm perfusion, endothelial function and leukocyte/thrombocyte activation after tourniquet-induced ischemia/reperfusion injury of the forearm are measured using healthy volunteers in a cross-over design.

Enrollment

10 estimated patients

Sex

Male

Ages

25 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria: male

  • Non-smoker
  • No asthma
  • NPO
  • Volunteer

Exclusion criteria:

  • Female
  • Chronic medication
  • Asthma
  • Smoking

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

01 Studienregister MasterAdmins

Data sourced from clinicaltrials.gov

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