At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 41 enrolled
Drug / intervention
Ginkgo biloba extract EGb 761drug
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.
Efficacy and Tolerability of Ginkgo Biloba Extract EGb 761® in Patients With Raynaud´s Phenomenon
In Brief
A Phase 2 clinical trial evaluating Ginkgo biloba extract EGb 761 for Raynaud Disease. Completed, enrolled 41 participants across 1 site.
Detailed Summary
The aim of the study is to investigate the efficacy and safety of EGb 761® in patients with the primary Raynaud phenomenon, with regards to the frequency, duration and severity of vasospastic attacks.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRaynaud Disease
CountriesNetherlands
Collaborators--
Timeline
Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartNov 2005
First PostedNov 2005
Primary CompletionMar 2006
Study CompletionApr 2006
TodayJul 2026
First PostedNov 9, 2005
Enrollment StartNov 1, 2005
Primary CompletionMar 1, 2006
Study CompletionApr 1, 2006
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 20.6 years ago
Interventions
Ginkgo biloba extract EGb 761drug
daily Ginkgo biloba extract EGb 761