Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis
Primary Purpose
Adenomyosis, Heavy Uterine Bleeding, Dysmenorrhea
Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ulipristal Acetate
Sponsored by
About this trial
This is an interventional treatment trial for Adenomyosis focused on measuring heavy periods, painful periods, adenomyosis
Eligibility Criteria
Inclusion Criteria
- 18-51 years old
- PBAC score greater than 100
- Ultrasound or MRI findings of adenomyosis
Exclusion Criteria
- Inability to comprehend written and/or spoken English or Spanish
- Inability to provide informed consent
- Current uterine, breast, cervical or ovarian cancer
- Unwilling to use contraception
- Positive pregnancy test or planning pregnancy during the study period
- Submucosal uterine fibroids (or greater than a certain size)
- Current premalignancy or malignancy
- Endometrial ablation or uterine artery embolization
- Known hemoglobinopathy
- Known severe coagulation disorder
- Large uterine polyp (>2cm)
- BMI >40
- Previous or current treatment with SPRM or GnRH agonist
- Progestins, acetylsalicylic acid, mefenamic acid, anticoagulants, antifibrinolytic drugs, systemic glucocorticoids within 1 month of enrollment
Sites / Locations
- Vanderbilt University Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Ulipristal
Arm Description
Ulipristal acetate 5mg daily for 12 weeks
Outcomes
Primary Outcome Measures
Bleeding patterns
Patient will use the pictorial blood loss assessment chart (PBAC) to describe bleeding patterns
Secondary Outcome Measures
Quality of life
Patient will complete menorrhagia impact questionnaire (0-100, 0 is worst and 100 is best quality of life)
Pain
Patient will complete pain scale (0-10, 0 is no pain and 10 is worst pain)
Full Information
NCT ID
NCT03325868
First Posted
October 25, 2017
Last Updated
February 6, 2018
Sponsor
Vanderbilt University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03325868
Brief Title
Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis
Official Title
Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Withdrawn
Why Stopped
IND issues
Study Start Date
February 2018 (Anticipated)
Primary Completion Date
May 2019 (Anticipated)
Study Completion Date
May 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Adenomyosis affects approximately 21% of symptomatic women who present to gynecology clinics. The disease is characterized by heavy bleeding and pain during periods. Limited treatment options exist for the treatment of adenomyosis for women who desire future child-bearing or prefer to avoid surgery. Recently, ulipristal acetate has been studied as a treatment option for women who have fibroids and heavy bleeding. The majority of women treated with ulipristal stopped having periods altogether. Our study aims to determine whether ulipristal is an adequate treatment for women with adenomyosis.
Detailed Description
Adenomyosis affects an estimated 20.9% of symptomatic women who present to gynecology clinics, with peak prevalence of 32% in 40-49 years old. Prior histologic studies in women undergoing hysterectomy show prevalence of with some variation due to differing histologic diagnostic criteria 10-37.1%. Heavy menstrual bleeding and dysmenorrhea are commonly manifested in women with adenomyosis. However, data on treatment of adenomyosis remains scarce. For women desiring definitive options, hysterectomy remains the treatment of choice. However, for women who desire future fertility, the currently accepted first-line therapy is progestogen therapy, particularly the levonorgestrel-IUD. Other limited studies have used danazol and GnRH agonists, but its use is limited by significant side effects.
Recently, the selective progesterone receptor modulators (SPRM) have emerged as successful medical treatment options for leiomyoma. The SPRM ulipristal acetate has been studied extensively in the treatment of leiomyoma and more recently endometriosis. Ulipristal acetate exerts both antagonist and agonist properties. Amenorrhea was achieved in 80% of women taking 5mg of ulipristal daily by treatment month 2 and up to 90% of women taking 10mg daily. Anovulation was achieved in 80% of women taking 5mg and 10mg dosing. Ulipristal acetate has not been studied as a treatment option for women with adenomyosis. We aim to study the effect of daily ulipristal on heavy menstrual bleeding in women with adenomyosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adenomyosis, Heavy Uterine Bleeding, Dysmenorrhea
Keywords
heavy periods, painful periods, adenomyosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ulipristal
Arm Type
Experimental
Arm Description
Ulipristal acetate 5mg daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Ulipristal Acetate
Other Intervention Name(s)
Fibristal
Intervention Description
Ulipristal 5mg daily by mouth for 12 weeks
Primary Outcome Measure Information:
Title
Bleeding patterns
Description
Patient will use the pictorial blood loss assessment chart (PBAC) to describe bleeding patterns
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Quality of life
Description
Patient will complete menorrhagia impact questionnaire (0-100, 0 is worst and 100 is best quality of life)
Time Frame
6 months
Title
Pain
Description
Patient will complete pain scale (0-10, 0 is no pain and 10 is worst pain)
Time Frame
6 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
51 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
18-51 years old
PBAC score greater than 100
Ultrasound or MRI findings of adenomyosis
Exclusion Criteria
Inability to comprehend written and/or spoken English or Spanish
Inability to provide informed consent
Current uterine, breast, cervical or ovarian cancer
Unwilling to use contraception
Positive pregnancy test or planning pregnancy during the study period
Submucosal uterine fibroids (or greater than a certain size)
Current premalignancy or malignancy
Endometrial ablation or uterine artery embolization
Known hemoglobinopathy
Known severe coagulation disorder
Large uterine polyp (>2cm)
BMI >40
Previous or current treatment with SPRM or GnRH agonist
Progestins, acetylsalicylic acid, mefenamic acid, anticoagulants, antifibrinolytic drugs, systemic glucocorticoids within 1 month of enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amanda Yunker, DO
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Study Director
Facility Information:
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis
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