EUCTR2011-006129-17-DEActive, not recruitingPhase 1
A randomized, double blind, placebo-controlled pilot study on the efficacy of Passiflora incarnata L. in an acute stressful situation - P. incarnata and stress - P1-2011
Conditions
Drugs
Trial Snapshot
- Phase
- Phase 1
- Status
- Active, not recruiting
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •healthy, non-smoking, 25-45, BMI>19<30, signed informed consent, females: oral contraceptives
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 60
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- •condition or medication that could put the subject at risk or interfere with the accuracy of the study results, participation in another clinical study, ability to speak for oneself lacks or can be doubted, women: pregnant or lactating
Investigators
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