Ischemia-Reperfusion
Conditions
Brief summary
The investigators will examine whether administration of certain medications will decrease or prevent ischemia-reperfusion injury.
Interventions
Sponsors
Maastricht University Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients undergoing breast reconstruction
Exclusion criteria
* Diabetes mellitus * Kidney or liver disease * Use of immunosuppressants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Antioxidant concentrations | 0,5-24 hours |
Countries
Netherlands
Contacts
Primary ContactMarieke van den Heuvel, M.D.
Backup ContactR. van der Hulst, M.D., Phd
Outcome results
None listed