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The Effect of Ulipristal Acetate (UPA) on Women Ovarian Reserve (UPA_ovAge)

Primary Purpose

Infertility

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
ulipristal acetate
Sponsored by
University Magna Graecia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring ovarian reserve, infertility, leiomyomas, ulipristal acetate

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • submucosal,
  • intramural or subserosal leiomyomas,
  • symptoms of menometrorrhagia,
  • menstrual disorder,
  • infertility,
  • pelvic pain

Exclusion Criteria:

  • endometrial hyperplasia with atypia,
  • estrogen-progestin therapy in the 2 months before enrollment,
  • autoimmune diseases,
  • chronic, metabolic, systemic and endocrine disorders, including hyperandrogenism, hyperprolactinemia, diabetes mellitus and thyroid disease,
  • hypogonadotropic hypogonadism,
  • majors clinical conditions

Sites / Locations

  • Azienda Ospedaliera Pugliese-CiaccioRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Ulipristal acetate

Arm Description

Women will be treated with 5mg/die of Ulipristal acetate for 2 courses of 3 months each

Outcomes

Primary Outcome Measures

Ovarian age change after two courses of UPA
Ovarian Age will be assessed as a composite outcome by measuring FSH, Estradiol, AMH, 3D-AFC, VI, FI and VFI (vascularization flow index) in the follicular phase of the menstrual cycle before the start of treatment. The assessment will be repeated during the fifth month of UPA assumption. change will be quantified

Secondary Outcome Measures

Full Information

First Posted
February 2, 2015
Last Updated
November 17, 2016
Sponsor
University Magna Graecia
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1. Study Identification

Unique Protocol Identification Number
NCT02361892
Brief Title
The Effect of Ulipristal Acetate (UPA) on Women Ovarian Reserve
Acronym
UPA_ovAge
Official Title
The Effect of UPA on Women Ovarian Reserve
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
September 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Magna Graecia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The uterine leiomyoma is the most common female benign disease.UPA seems to be most effective for the medical management of fibroids and could be place as preoperative adjunct to surgery but also as medical therapy to avoid surgery. No data have been published about the effect of UPA on FSH (Follicle stimulating hormone) or AMH levels nor on ovarian antral follicle count (AFC) or vascularization indexes during and after treatment. Considering that in young women of reproductive age (under 40 years old), desiring pregnancy, UPA has been proposed to avoid or postpone surgery, also in a long-term administration program, data about its effect on women ovarian reserve are urgently needed. For these reasons, data on biochemical (AMH, FSH and E2) and 3D ultrasonographic (VI, Flow index, AFC) parameters of women treated by UP are needed to assess the effect of the drug in terms of ovarian reserve modification.
Detailed Description
The uterine leiomyoma is the most common benign tumor of the female genital tract. The myomas are usually clinically apparent in 25% of patients. Among the latest possible therapeutic options, UPA has proved to be most effective for the medical management of fibroids. Its advent in the clinical practice will probably modify the surgical approach, since UPA could possible place as a preoperative adjunct to surgery but also as medical therapy to avoid surgery. Very recently, the results of the first study on long-term intermittent (18 months) therapy with 10-mg UPA were published, demonstrating that this regimen (four courses of 3 months) maximizes the effect of UPA by inducing a very high rate of amenorrhea and reducing fibroid size. Long term treatment, however, call in question safety issue that need to be explore. In patients treated by UPA, Estradiol under 5-mg and 10-mg doses remained at midfollicular levels after the first course of therapy, avoiding menopausal symptoms, as frequently observed in the gonadotropin-releasing hormone (GnRH-) agonist group. No data have been published about Estradiol levels at the end of second, third and fourth courses of UPA. Moreover, no data have been published about the effect of UPA on FSH or AMH levels nor on ovarian antral follicle count (AFC) or vascularization indexes during and after treatment. Considering that in young women of reproductive age (under 40 years old), desiring pregnancy, UPA has been proposed to avoid or postpone surgery, also in a long-term administration program, data about its effect on women ovarian reserve are urgently needed. For these reasons, data on biochemical (AMH, FSH and E2) and 3D ultrasonographic (VI, FI, AFC) parameters of women treated by UP are needed to assess the effect of the drug in terms of ovarian reserve modification.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
ovarian reserve, infertility, leiomyomas, ulipristal acetate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
73 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ulipristal acetate
Arm Type
Experimental
Arm Description
Women will be treated with 5mg/die of Ulipristal acetate for 2 courses of 3 months each
Intervention Type
Drug
Intervention Name(s)
ulipristal acetate
Other Intervention Name(s)
Esmya
Intervention Description
5 mg/day will be administered starting from day 1 of the cycle for two courses of 3 months each
Primary Outcome Measure Information:
Title
Ovarian age change after two courses of UPA
Description
Ovarian Age will be assessed as a composite outcome by measuring FSH, Estradiol, AMH, 3D-AFC, VI, FI and VFI (vascularization flow index) in the follicular phase of the menstrual cycle before the start of treatment. The assessment will be repeated during the fifth month of UPA assumption. change will be quantified
Time Frame
In the follicular phase of the month before treatment and during the fifth month of treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: submucosal, intramural or subserosal leiomyomas, symptoms of menometrorrhagia, menstrual disorder, infertility, pelvic pain Exclusion Criteria: endometrial hyperplasia with atypia, estrogen-progestin therapy in the 2 months before enrollment, autoimmune diseases, chronic, metabolic, systemic and endocrine disorders, including hyperandrogenism, hyperprolactinemia, diabetes mellitus and thyroid disease, hypogonadotropic hypogonadism, majors clinical conditions
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fulvio Zullo, MD,PhD
Phone
00390961883234
Email
zullo@unicz.it
First Name & Middle Initial & Last Name or Official Title & Degree
Roberta Venturella, MD
Phone
00390961883401
Email
rovefa@libero.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fulvio Zullo, MD,PhD
Organizational Affiliation
Magna Graecia University of Catanzaro
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Roberta Venturella, MD
Organizational Affiliation
Magna Graecia University of Catanzaro
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliera Pugliese-Ciaccio
City
Catanzaro
ZIP/Postal Code
88100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fulvio Zullo
Phone
00390961883234
Email
zullo@unicz.it

12. IPD Sharing Statement

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The Effect of Ulipristal Acetate (UPA) on Women Ovarian Reserve

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