EQUIPT: Evaluating Quality of life In Period Treatment

K
Kerry Hege, MD

Primary Investigator

Enrolling By Invitation
9-21 years
Female
Phase N/A
100 participants needed
2 Locations

Brief description of study

The primary objective is to characterize the comparative effectiveness of hormonal therapy (combined oral contraceptives and progesterone methods), antifibrinolytic therapy, and intrauterine devices in the treatment of heavy
menstrual bleeding (HMB) in adolescent females with an underlying bleeding disorder.

Detailed description of study

Who is Eligible to Participate:
 
Natal female, with uterus present, and menstruating 
Age 9-21 years 
Self-reported heavy menstrual bleeding 
Diagnosed bleeding disorder OR undergoing evaluation for a bleeding disorder
 
 
What is Involved:
 
For this study you will be asked to complete surveys at three different times, more often if you begin new medications. These surveys will ask you questions about your health, your therapy, and your menstrual cycle.
We will also look at your medical records so we can better understand your health and medical history.  Surveys may be completed via email.
 
This study will take place at Riley Hospital for Childrenand will last for 15 months.
 
 
Compensation:
 
You will receive a $10 gift card after completion of the enrollment survey and an additional $10 gift card after completion of the final survey, for a total of $20 for participation in the study.
 
 
 
 
 

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: menorrhagia,von Willebrand disease,hemophilia, Riley
  • Age: Between 9 Years - 21 Years
  • Gender: Female

Inclusion Criteria:
Natal female, with uterus present, and menstruating 
Age 9-21 years 
Self-reported heavy menstrual bleeding 
Diagnosed bleeding disorder OR undergoing evaluation for a bleeding disorder
 
 
Exclusion Criteria: 
Currently pregnant or has been pregnant in the past 3 months 
Bleeding disorder previously ruled out 
On current menstrual suppression >12 months (known bleeding disorder) or >60 days (bleeding disorder evaluation) 
Current anticoagulation treatment

Updated on 13 Sep 2024. Study ID: 12874, PHO-EMORY-EQUIPT
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