The purpose of this study is to evaluate the safety, tolerability and efficacy of TT-173 in
healthy volunteers after tooth extraction.
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Locations near you
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Full eligibility criteria for NCT01595360
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Subjects to be undertaken for the simple extraction of at least one tooth (incisor, canine, premolar, molar different of third molar) that cause bloody wound, located in the upper or inferior maxillary area of the mouth either
Subjects who are able and willing to provide written and signed informed consent
All subjects willing to use a medically accepted form of contraception from the time of consent to completion of all follow-up study visits. Negative pregnancy test result in the screening visit.
Subjects with personal and family history that could affect correct hemostasis
Subjects with any clinically-significant coagulation disorder including including deficiencies in any of coagulation factors, thrombocytopenia and vascular purpura
Subject with hipersensivity of TT-173 of any of its components or has a known allergy.
Subjects who are unable to adequately follow or understand the instructions and requirements of the study.
Subjects that are not fully free to give informed consent, or any other obstacle in the opinion of investigator support the conclusion that the subject is not fully reasoned.
All locations for NCT01595360
Thrombotargets Europe SL
Castelldefels, Barcelona, Spain, 08860
View full eligibility
Tris trial is registered with FDA with number: NCT01595360. The sponsor of the trial is Thrombotargets Europe S.L and it is looking for 24 volunteers for the current phase.
Official trial title: A Phase 1, Randomized, Open, Controlled, Comparative Safety, Tolerability and Efficacy Study of TT-173 in Healthy Volunteers After Tooth Extraction
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