Inherited prekallikrein deficiency

MONDO:0012901

An instance of prekallikrein deficiency that is caused by an inherited modification of the individual's genome.

Also known as: congenital prekallikrein deficiency, fletcher factor (prekallikrein) deficiency, hereditary prekallikrein deficiency, Fletcher Factor deficiency, PKK deficiency, prekallikrein deficiency, prekallikrein deficiency, congenital

12 clinical trials for this condition and its sub-types, 0 tagged with Inherited prekallikrein deficiency itself.

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Where it sits in the disease tree

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Part of

↑ Hemorrhagic disease (510) ↑ Inherited blood coagulation disorder (323) ↑ Coagulation protein disease (274) ↑ Prekallikrein deficiency (0)

Including sub-types (12) Tagged with Inherited prekallikrein deficiency (0)

Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2

Ginger vs. heavy periods: a natural approach for women with bleeding disorders

Symptom relief Not yet recruiting

This study tests whether taking ginger powder for the first three days of each period can reduce heavy menstrual bleeding in women with coagulation disorders (bleeding problems). 74 women will be randomly assigned to receive either ginger or a placebo for six cycles. The goal is …

Early phase 1 • Sponsor: University of Valladolid • Aim: Symptom relief

Last updated Jun 27, 2026 12:35 UTC

Inherited prekallikrein deficiency

Where it sits in the disease tree

Ginger vs. heavy periods: a natural approach for women with bleeding disorders