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Evaluation of the prophylactic effect of tranexamic acid in von willebrand disease and glanzman thrombasthenia

Evaluation of the prophylactic effect of tranexamic acid in von willebrand disease and glanzman thrombasthenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015111525031N2
Enrollment
20
Registered
2015-12-05
Start date
2014-07-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Glanzmann thrombasthenia. Condition 2: Von Willebrand. Qualitative platelet defects Von Willebrand disease

Interventions

Intervention 1: for six months, patients treated with tranexamic acid capsules manufactured by Amin-drug, daily 25 mg per kilogram of body up to 500 mg placed in a single dose. Intervention 2: for six
Treatment - Drugs
Placebo
for six months, patients treated with tranexamic acid capsules manufactured by Amin-drug, daily 25 mg per kilogram of body up to 500 mg placed in a single dose
for six months use tranexamic acid capsules that filled with starch as placebo

Sponsors

Vice Chancellor for research of Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients with a von Willebrand I, II, III and Glanzmann thrombasthenia which they records are included in Arak Amir-Kabir Hospital.; Exclusion criteria: (a)Patients who have a history of thrombosis; (b)Patients who do not consent to the inclusion; (c)Patients with hepatitis B or C; (d)Patients with liver or renal dysfunction; (e)Patients with local bleeding lesions such as hemangiomas or local wound; (f)Younger than 2 years; (g)Patients who can not tolerate the gastrointestinal drug;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The number of bleeding attacks. Timepoint: before and six months after intervention. Method of measurement: counting frequency.;The severity of bleeding. Timepoint: before and six months after intervention. Method of measurement: visual scale and assigned a grade from one to four.;The number of used concentrates. Timepoint: before and six months after intervention. Method of measurement: counting frequency.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Laura Melikof

Arak University of Medical Sciences

sun14039@yahoo.com+98 86 3313 5075

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026