Trials / Completed
CompletedNCT02862236
The Acute Effect of Hypericum Perforatum on Short-Term Memory in Healthy Adults
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 104 (actual)
- Sponsor
- Prof. Eldad Yechiam · Academic / Other
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
Rationale Over-the-counter drugs containing hypericum perforatum (H. perforatum), have been argued to improve memory and sustained attention. So far, these claims have not been supported in human studies. However, previous studies used rather high dosages, and little is known about the acute effect of small dosages. Objective We evaluated whether an acute treatment with Remotiv 500 and Remotiv 250 (500 or 250 mg of H. perforatum quantified to either 1 or 0.5 mg of hypericin) improved memory, sustained attention, as well as mood and state anxiety in healthy adults. Method A single dosage, randomized, double blind, placebo-controlled trial was conducted with 82 student participants (33 women). Each participant received placebo in one session and one of two dosages in the other session. Order of the sessions and dosage conditions were randomized between subjects. Participants completed a battery of tasks assessing short-term memory capacity and sustained attention.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Hypericum perforatum extract | 250 or 500 mg Remotiv capsules of hypericum perforatum extract, p.o. |
Timeline
- Start date
- 2017-02-21
- Primary completion
- 2018-02-02
- Completion
- 2018-02-02
- First posted
- 2016-08-10
- Last updated
- 2018-09-14
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT02862236. Inclusion in this directory is not an endorsement.