Tranexamic Acid in Adolescents With Heavy Menstrual Bleeding

Completed · Phase 4

Conditions studied: Heavy Menstrual Bleeding

In brief

This is a study to learn more about a drug called Tranexamic acid (TA), otherwise known as Lysteda, and whether or not this drug can decrease menstrual blood loss in young women and lead to an increase in the quality of life. Menorrhagia in young women with bleeding disorders is typically treated with a combination of treatments including hormonal contraceptives. However, there are barriers to hormonal contraception use in younger adolescents. Tranexamic acid is taken orally during the first 5 days of menstrual bleeding. The purposes of this study include: To test the safety and efficacy of Lysteda in adolescent females. To learn how well Lysteda works in decreasing menstrual blood loss. To see if parents and children participating in this study think the drug is improving their quality of life. Lysteda has been approved by the Food and Drug Administration for use in patients \> than 18 years of age but not for younger patients.

Key facts

Study ID

NCT01846507

Run by

Nationwide Children's Hospital

People needed

32

Starts

2013-04-01

Expected to finish

2016-11-01

Last updated by the study team

2018-10-24

Who can join

Age: 10 and older, up to 19. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Menstruating females 10-19 years of age
• Non-smoker
• Physician and patient have agreed to initiate Lysteda
• Diagnosis of HMB based on the medical judgment of the principal or site investigator
• Subjects must report menstrual periods occurring within 21-60 days from the start of one period to the start of the next menstrual period
• Negative pregnancy test
• Informed consent obtained and signed
• Informed assent obtained and signed
• Understanding of study procedures
• Ability to comply with study procedures for the entire length of the study
• Subjects should be either sexually inactive (abstinent) or agree to use a barrier method with spermicide in the event of sexual activity throughout the study period

You may not qualify if…

• Active thromboembolic disease, history of thromboembolic disease (including retinal vein or artery occlusion), known inherited thrombophilia, or family history of thrombosis in a first degree relative
• Subject has a severe medical or psychiatric illness that, in the opinion of the Investigator, would affect subject safety or compliance
• Clinical evidence of severe bleeding disorder. Patients with mild bleeding disorders such as type 1 von Willebrand disease, mild platelet function defects such as platelet storage pool or release defects, and patients with bleeding due to Ehlers Danlos syndrome WILL be eligible to participate in the study.
• Pregnancy within the past 6 months and/or breast-feeding
• Use of hormonal contraception (estrogen and progestin) within 3 months of study entry, or anticipated need to initiate estrogen-containing hormonal contraception during the study period
• Use of systemic steroids within 1 month of study entry
• History of subarachnoid hemorrhage
• History of Hepatitis B, C, or HIV
• Baseline creatinine >20% above the upper limit of normal for age
• Severe anemia (hemoglobin <8 g/dL)
• Systolic blood pressure <85 or diastolic blood pressure <55
• Heart rate <50 at time of screening
• Use of intranasal DDAVP during menses will be permitted, but only if the patient has a history of using DDAVP consistently for ≥3 menstrual cycles prior to study enrollment, so that change in menstrual blood loss due to addition of Lysteda can be assessed. Use of one-time DDAVP during a DDAVP/Stimate challenge is also permitted during the study period, as is use of DDAVP in the event of severe epistaxis, trauma, or surgical procedures during the study period.

Where it is running

• Riley Hospital for Children at IU Health — Indianapolis, Indiana, United States
• Children's Mercy Hospital — Kansas City, Missouri, United States
• Akron Children's Hospital — Akron, Ohio, United States
• Rainbow Babies & Children's Hospital — Cleveland, Ohio, United States
• Nationwide Children's Hospital — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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