The Assessment of Fibrin Clot Phenotype and Thrombin Generation in Women After Urogynecological Surgeries.

Recruiting Observational Study
Uterine Prolapse Urine Incontinence
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 70
Sex
Female
Study type
Observational
Participants needed
60 (estimated)
Sponsor
Jagiellonian University · Other
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About This Trial

Determination of fibrin clot properties along with thrombin generation in women after urigynecological surgery.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 18-70 * treatment failure (pharmacotherapy) due to uterine prolapse or urine incontinence Exclusion Criteria: * prolonged thromboprophylaxis * planned surgery other than due to urine incontinence/uterine prolapse * acquired or congenital thrombophilia
Contacts

Magdalena MP Piróg, MD, PhD

+48 604514915

magda.m.pulka@gmail.com

CONTACT