Skip to main content
OpenTrials
Completed

NCT Number: NCT05049447

Pharmacological Effects of Pascoflair® on Brain Activity in Patients Suffering From Test Anxiety

Proof of effectiveness of Pascoflair using qantitative measurement of electric brain activity during examination stress in 40 subjects suffering from test anxiety. A double-blind, randomized, placebo-controlled, 2-armed, Phase IV study in parallel design.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

About this study

Anxiolytic effects of PASCOFLAIR® shall be tested in subjects suffering from test anxiety after single intake by aid of a newly developed, validated method consisting of a combination of eye tracking (following glances) with neurocode tracking (quantitative EEG with a time resolution of 364 ms).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy male and female subjects.
  • Age between 18 and 40 years (both included).
  • Anxiety questionnaire PAF (pre-selection of subjects) - values above T> 60 are regarded as conclusive.
  • Inconclusive case history and diagnosis.
  • Subject must be capable of giving informed consent.
  • Acceptance of written consent to participate in the study after education in written and oral form (informed consent).

Exclusion criteria

  • Acute or chronic disease with an impact on the study, which becomes obvious by case history or clinical examination.
  • Clinically relevant pathological findings from clinical and laboratory findings.
  • Presence of clinically relevant pathological EEG features or artifact-free portion of the screening EEG <30%.
  • Clinically relevant allergic symptoms.
  • Detection of alcohol at the time of initial examination (day SC) or on study day A (positive alcohol test) or by case history.
  • Detection of drugs (positive drug test) at the time of initial examination (day SC).
  • Consumption of clinically relevant medication during last fourteen days before and during the active study period based on the notification of the subject or his case history.
  • Consumption of medication with primarily central action (i.e. psychotropic drugs or centrally acting antihypertensives).
  • Known intolerance / hypersensitivity (allergy) to plant derived extracts (Passion flower dry extract) or any of the ingredients of the investigational product (anamnestic).
  • Presence of a rare, genetic disease such as fructose intolerance, glucosegalactose malabsorption or sucrase-isomaltase deficiency (anamnestic).
  • BMI (Body Mass Index) <18 or> 32.
  • Consumption of unusual quantities or misuse of coffee (more than 4 cups a day), tea (more than 4 cups a day) or tobacco (more than 20 cigarettes per day).
  • Smoking on day of A.

Treatment and study plan

Pascoflair

Drug

1 x 2 tablets (single-dose)

Placebo

Other

1 x 2 tablets (single-dose)

Primary outcomes

  1. Comparison of verum and placebo Beta 1 power

    Time frame: day A (treatment day) - 1 day

    Comparison of verum and placebo efficacy is performed on electric power in 17 different brain regions within six frequency ranges defined as target parameters in the presence of different stress inducing cognitive tests or exciting video scenes

Secondary outcomes

  1. Tolerability in a 4- Point scale

    Time frame: Final examination (day AB) -1 day

    Tolerability in a 4- Point scale (very good, good, moderately, poor)

  2. Correlation between questionnaire items and spectral EEG power with regard to different frequency ranges.

    Time frame: Final examination - 1 day

    Correlation between questionnaire items and spectral EEG power with regard to different frequency ranges.

Sponsors and collaborators

Lead sponsor

Pascoe Pharmazeutische Praeparate GmbH

Industry

Collaborators

  • NeuroCode AG

Registry information

Official study title

Proof of Effectiveness of Pascoflair Using Qantitative Measurement of Electric Brain Activity During Examination Stress in 40 Subjects Suffering From Test Anxiety. A Double-blind, Randomized, Placebo-controlled, 2-armed, Phase IV Study in Parallel Design.

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Sep 20, 2021
Registry last updated
Sep 20, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.