NCT01665170

Pilot Study on the Efficacy of Pascoflair in an Acute Stressful Situation (TSST)

A Randomized, Double Blind, Placebo-controlled Pilot Study on the Efficacy of Passiflora Incarnata L. in an Acute Stressful Situation

• Status: Completed
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 60 (actual)
• Sponsor: Pascoe Pharmazeutische Praeparate GmbH · Industry
• Sex: All
• Age: 25 Years – 45 Years
• Healthy volunteers: Accepted

Summary

A randomized, double blind, placebo-controlled pilot study on the efficacy of Passiflora incarnata L. in an acute stressful situation

Detailed description

Randomized, double-blind, placebo-controlled, single-center study During Visit 1 study information and an informed consent form are handed out. After study inclusion on Visit 2, participants are assigned to one of two groups at random and receive the test products (either Pascoflair® or placebo tablets). The 3rd visit includes the completion of questionnaires regarding wellbeing and the Trier Social Stress Test.

Conditions

• Healthy
• Stress

Interventions

Type	Name	Description
DRUG	Passiflora incarnata	3 x 1 tablet per day for 3 days
DRUG	Placebo	3 x 1 ablet per day for 3 days

Timeline

• Start date: 2012-05-01
• Primary completion: 2012-08-01
• Completion: 2012-08-01
• First posted: 2012-08-15
• Last updated: 2015-12-09
• Results posted: 2015-12-09

Locations

1 site across 1 country: Germany