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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05477472
Other study ID # OS01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2005
Est. completion date January 2007

Study information

Verified date July 2022
Source Ceres Heilmittel AG
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This observational study observes the routine use of low-dose St John's Wort herbal mother tincture in patients with major depression. It measures intensity of depression at the beginning of St Johns Wort and after 6 weeks and evaluates tolerability and compliance.


Description:

Herbal medicine is widely used, and high-quality evidence shows their efficacy and tolerability for specific disorders. Most of the studies, however, is conducted with standardized, relatively high dosed dry extract preparations, while other preparations such as tinctures are widely used as well. The aim of this observational study ist to document real-live use of the use of a low-dose herbal medicine preparation (a mother tincture) of St John's Wort (Hypericum perforatum), to compare depression intensity at the beginning and after 6 weeks of therapy using the Hamilton Depression Scale 17, and to evaluate tolerability and compliance. Finally, the results will be compared with results of randomized controlled trials examining high dosed dry extract preparations of St John's Wort for major depression.


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date January 2007
Est. primary completion date January 2007
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - diagnosis of mild or moderate depression according to ICD-10 or DSM-IV - new start of CERES St John's wort mother tincture Exclusion Criteria: - at the same time as St John's wort mother tincture started, other antidepressive therapy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
St John's Wort
daily intake of CERES St John's Wort mother tincture. Dose according to the treating physician.

Locations

Country Name City State
Switzerland CERES Heilmittel AG Kesswil Thurgau

Sponsors (2)

Lead Sponsor Collaborator
Ceres Heilmittel AG University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hamilton Depression Scale 17 validated tool to measure depression intensity. Maximum score 51, minimum 0. Higher score means higher intensity of depressive symptoms. Change at 6 weeks
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