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Clinical Trials/EUCTR2005-000687-77-DE
EUCTR2005-000687-77-DE
Active, not recruiting
Not Applicable

Pilotstudie zur Verträglichkeit und Effektivität eines Artischockenpräparates bei Patienten mit chronischer Hepatitis C

ni-Zentrum naturheilkunde0 sites16 target enrollmentApril 28, 2005
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DrugsHepar SL forte

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
ni-Zentrum naturheilkunde
Enrollment
16
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 28, 2005
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
ni-Zentrum naturheilkunde

Eligibility Criteria

Inclusion Criteria

  • •Serologisch gesicherte chronische Hepatitis C
  • •Alanin Aminotransferase bei 2 Kontrollen innerhalb 4 Monaten vor Studienbeginn \>1,5 fach des oberen Normwertes erhöht
  • •Alter 18\-75 Jahre
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •Interferonhaltige Therapie geplant oder in den letzten 3 Monaten vor Studienbeginn
  • •Leberzirrhose Child B oder C
  • •Alkoholkonsum \>30 g/Tag, Drogenabusus
  • •Schwere Begleiterkrankungen

Outcomes

Primary Outcomes

Not specified

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