CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 45 enrolled
Drug / intervention
Souroubea-Platanus Preparation +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03904511
NCT03904511Phase 1Completed

Safety, Tolerability and Behavioural Effects of Souroubea-Platanus in Healthy Volunteers

University of Ottawa·interventional·Posted Apr 5, 2019·Updated Feb 11, 2020

In Brief

A Phase 1 clinical trial evaluating Souroubea-Platanus Preparation and Placebo for Anxiety and Stress, Psychological. Completed, enrolled 45 participants across 1 site.

Detailed Summary

Souroubea sympetala extracts have shown anxiolytic properties in animal models. Souroubea and its active principle betulinic acid appear to exert these effects by acting as an agonist for the benzodiazepine (BZD) binding site of the GABAA receptor with no withdrawal effects on food intake, locomotor activity, or other symptoms typically associated with BZD agonism. As such, this may offer a valuable source for an alternative anti-anxiety treatment. The primary objective of this study is to (1) to evaluate the safety and tolerability of a single daily dose of an extract of a mixture of Souroubea spp. leaf and small branch material and Platanus spp. bark when administered orally over two weeks in healthy volunteers. Based on its safety in canine trials, we hypothesize that Souroubea-Platanus (SP) preparation will be well tolerated with adverse event profile similar to placebo. The secondary objective is (2) to establish whether some of the anxiolytic properties of Souroubea-platanus seen in animal models will translate to human participants. We hypothesize that Souroubea-Platanus preparation will demonstrate anxiolytic and/or stress-reduction properties as indicated by salivary cortisol levels and self-report measures of anxiety.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

Phase 1CompletedFinished
2020202120222023202420252026
First PostedApr 5, 2019
Enrollment StartMay 15, 2019
Primary CompletionDec 31, 2019
Study CompletionFeb 1, 2020
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 7.2 years ago

Interventions

Souroubea-Platanus Preparationother

Extracts of S. Sympetala and P. occidentalis.

Placeboother

Placebo