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Estradiol vs Lysteda in Treatment of Heavy Menstrual Bleeding

Estradiol Versus Tranexamic Acid on the Amount and Duration of Acute Cyclic Heavy Menstrual Bleeding

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01659008
Enrollment
100
Registered
2012-08-07
Start date
2012-06-30
Completion date
2016-03-31
Last updated
2015-02-16

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

Conditions

Menstrual Cycle and Uterine Bleeding Disorders

Keywords

acute cyclical heavy menstrual bleeding

Brief summary

Treatment with Estradiol is non-inferior to treatment with Tranexamic acid in reducing the amount and duration of menstrual blood loss in women with cyclic heavy menstrual bleeding

Detailed description

BACKGROUND: The acute onset of Heavy Menstrual Bleeding (HMB) during menses results in women seeking care in the Emergency Department. The current management of HMB among our residents uses combination oral contraceptives or oral progestins. The residents in the Emergency Department often send women home without any therapeutic intervention. There is no Regulatory Agency approved therapy for acute HMB. The etiology of HMB is not well understood. Two potential causes are changes in endometrial prostaglandins and increased fibrinolytic activity in the endometrium. Specific Aim 1 is to investigate and compare the effect of oral estradiol compared to tranexamic acid in reducing blood loss and the duration of bleeding during an acute episode HMB. Specific Aim 2 is to evaluate the effect of estradiol and tranexamic acid on possible causes of the acute HMB by measuring prostaglandins and Plasminogen activator in menstrual effluent at the end of treatment. METHODS: This is a randomized, double-blind, controlled, parallel-group, non-inferiority trial, with participants between the ages 18 and 45 years, with acute cyclic heavy menstrual bleeding enrolled during an emergency room visit. Participants are randomized to receive 48 hours' treatment with 1.3 mg oral tranexamic acid or 1.0 mg oral estradiol three times a day. The primary endpoint is reduction in the amount of menstrual effluent. Sample size was calculated based on detecting less than 30 ml difference between the mean menstrual blood loss of the two treatment groups. Amount of blood loss is quantified by alkaline hematin method on extraction of menstrual pads and tampons. Secondary outcome is the variation of hemostatic factors in the menstrual effluent in two treatment groups by collecting menstrual effluent and quantitating prostaglandins, Plasminogen activators, Plasminogen activator inhibitors, and vascular endothelial growth factor. ANTICIPATED OUTCOMES: The investigators anticipate a reduction in mean menstrual blood loss in both treatment groups. Compared with participants treated with estradiol, the group treated with tranexamic acid will not have statistically significant change in reduction of menstrual effluent. We also anticipate changes in different local hemostatic factors in menstrual effluent specific to the treatment arm.

Interventions

DRUGEstradiol
DRUGLysteda

Sponsors

American College of Obstetricians and Gynecologists
CollaboratorOTHER
Kay I Waud MD PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Age: between 18-45 years old * Hemoglobin concentration: less than or equal to 11.5 g/dL, greater than or equal to 8.0 g/dL * BMI: less than or equal to 35 * Menstrual cycle: previous menstrual cycle interval between 26 to 34 days with less than or equal to 10 days of bleeding * Contraception: at least two months from implant removal, or six months from their last depo-provera or depo-Lupron injection, or recently(at least 2 months) discontinued oral, patch or intravaginal ring contraceptives * On cycle day 1-3 of the current menstrual bleeding episode

Exclusion criteria

* NSAID, or aspirin containing medications during the 48 hours preceding the current ER visit * Estrogen or progestin treatment during the 30 days preceding the current ER visit * Using Paraguard * Pregnant and or lactating * History of endometrial ablation * Women with thromboembolic disease, or coagulopathy * Women with history of myocardial infarction, or cerebrovascular occlusion * Uncontrolled high blood pressure (blood pressure greater than 150/90) * Sensitivity to estrogen, or tranexamic acid

Design outcomes

Primary

MeasureTime frameDescription
menstrual blood loss48 hoursreduction in mean menstrual blood loss in both treatment groups

Secondary

MeasureTime frameDescription
changes in local hemostatic factors48 hourschanges in local, endometrial hemostatic factors in both treatment groups

Countries

United States

Contacts

Primary ContactKay I Waud, MD PhD
waudk@evms.edu3103820090
Backup ContactDavid F Archer, MD
archerdf@evms.edu7574467444

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026