Trials / Completed
CompletedNCT01031992
Tranexamic Acid and Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT)
Efficacy of Tranexamic Acid Taken Orally in Patients With Hereditary Hemorrhagic Telangiectasia
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 23 (actual)
- Sponsor
- University Hospital, Saarland · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Hereditary hemorrhagic telangiectasia (HHT, Rendu-Osler-Weber Syndrome) is associated with frequent nosebleeds in the majority of cases. Several reports in the literature support the use of antifibrinolytics like Tranexamic acid to reduce nosebleeds. The objectives of the study are to test if Tranexamic acid taken orally can 1. improve anemia (lead to an increased hemoglobin level) 2. reduce nosebleeds.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Tranexamic acid first, than placebo | For 3 months Tranexamic acid 3 times daily 1 g taken orally, followed by placebo for 3 months. |
| DRUG | First placebo, than Tranexamic acid. | First placebo for 3 months, than tranexamic acid 3 times daily 1 g for 3 months. |
Timeline
- Start date
- 2002-03-01
- Primary completion
- 2002-08-01
- Completion
- 2002-10-01
- First posted
- 2009-12-15
- Last updated
- 2009-12-15
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01031992. Inclusion in this directory is not an endorsement.