Last updated: May 6, 2024
Sponsor: Sanquin-LUMC J.J van Rood Center for Clinical Transfusion Research
Overall Status: Completed
Phase
N/A
Condition
Soft Tissue Infections
Treatment
Protoporphyrin IX - Triplet State Lifetime Technique
Clinical Study ID
NCT03842722
NL64824.058.18
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age of patient is at least 18 years
- Patients diagnosed with sepsis in the emergency department or hospital ward
- Patients are admitted to the ICU via the hospital ward or emergency department
- Informed consent is given either by the patient or if the patient is too ill to giveinformed consent, by his or her legal representative.
- Patients have an arterial catheter in situ, since blood samples will be taken for thestudy. Most patients admitted to the ICU have an arterial catheter in place since itis part of standard care.
Exclusion
Exclusion Criteria:
- Patients younger than 18 years
- Patients with sepsis discharged after emergency department visit
- Patients admitted to a hospital ward other than the ICU after emergency departmentvisit
- Patients who cannot give informed consent themselves and without a legalrepresentative will be excluded since no informed consent can be obtained
- Patients known with porphyria and/or photodermatosis will be excluded, since the riskof phototoxicity
- Patients with hypersensitivity to the active substance or to the plaster material ofALA (5-aminolevulinic acid)
- Pregnant or breast feeding women since there is no adequate data form the use of ALAin pregnant or breast feeding women
- Insufficient comprehensibility of the Dutch language
Study Design
Total Participants: 81
Treatment Group(s): 1
Primary Treatment: Protoporphyrin IX - Triplet State Lifetime Technique
Phase:
Study Start date:
February 13, 2019
Estimated Completion Date:
September 28, 2023
Study Description
Connect with a study center
Leiden University Medical Center
Leiden, 2333 ZA
NetherlandsSite Not Available

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