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Clinical Trials/EUCTR2011-006129-17-DE
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

PASCOE Pharmazeutische Präparate GmbH0 sites60 target enrollmentStarted: March 8, 2012Last updated:
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Conditions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Enrollment
60
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

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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