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Ulipristal Acetate Versus GnRH Analogue and Myometrial Preservation

Primary Purpose

Fibroid

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

About this trial

This is an interventional treatment trial for Fibroid focused on measuring fibroid, GnRH analogue, ulipristal acetate

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

G2 submucosal leiomyoma <3 cm, symptoms of menomethrorragia, menstrual disorder, infertility, pelvic pain

Exclusion Criteria:

submucosal leyomyoma other than G2 or greater than 3 cm, intramural or subserosal leiomyomas endometrial hyperplasia with atypia history of uterine surgery

Sites / Locations

  • Azienda Ospedaliera Pugliese-CiaccioRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ulipristal acetate

Leuprolile acetate

Arm Description

Women will be treated with an oral dose of ulipristal acetate 5 mg/day for 2 courses of 3 months each

Women will be treated with an injection IM on leuprolide acetate 11,25 in the luteal phase repeated 3 months later

Outcomes

Primary Outcome Measures

Proportion of restored uterine cavity 1 year after enrollment
To compare the proportion of patients, treated by UPA or by GnRh-a, with uterine cavity no longer distorted by their submucous myoma

Secondary Outcome Measures

Time to pregnancy
to compare time to pregnancy in patients treated with Ulipristal Acetate and GnRH-a
Live birth rate
to compare live birth rate in patients treated with Ulipristal Acetate and GnRH-a
Proportion of patients needing surgery after UPA or GnRH-a
to compare need for surgery in patients treated with Ulipristal Acetate and GnRH-a.

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
NCT02357563
Brief Title
Ulipristal Acetate Versus GnRH Analogue and Myometrial Preservation
Official Title
Ulipristal Acetate Versus GnRH Analogue for Myometrial Preservation in Patients With Submucosal Uterine Leiomyoma G2
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
September 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
Submucosal fibroid grow inside the uterine cavity and are associated with menorrhagia, abnormal uterine bleeding (AUB) and infertility. Type II (G2) fibroids often require more surgeries due to their particular position in the myometrium. Surgery, moreover, should always be tailored, particularly in patients wishing to conceive, to preserve the integrity of the myometrium. Preoperative use of GnRH agonist appears to be relevant and beneficial in patients with submucous fibroids, but are associated with several side effects. the eighty percent of patients treated by UPA showed a clinically meaningful reduction of more than 25% in fibroid volume, and 50% of patients a reduction of 50%. fibroid volume reduction appeared to be maintained for 6 months after the end of UPA treatment
Detailed Description
Uterine leiomyoma is the most common benign tumor of the female genital tract. Submucosal fibroid are about 10% of all uterine myoma. They grow inside the uterine cavity and are usually associated with menorrhagia, abnormal uterine bleeding (AUB) and infertility. According to the degree of myometrial penetration, the European Society for Gynaecological Endoscopy (ESGE) classified submucosal myomas in Type 0 (G0, totally intracavitary fibroids), Type I (G1, <50% myometral penetration), or Type II (G2, >50% myometral penetration). Hysteroscopic removal of submucosal myomas improves menorrhagia and AUB but can be challenging in women with Type II (G2) fibroids, since they often require more and more surgeries due to their particular position in the context of myometrium. Surgery, moreover, should always be tailored, particularly in patients wishing to conceive, to preserve the integrity of the myometrium. In this particular population, indeed, the possibility of avoiding any kind of uterine surgery should always be exploited. Up to now, hysteroscopic resection of submucosal fibroids is considered the gold standard for symptomatic patients, since no medication has been able to restore uterine cavity in a permanent manner. In this setting, use of a GnRH agonist before surgery is still a matter of debate, but literature reports that preoperative use of GnRH agonist appears to be relevant and beneficial in patients with submucous fibroids. Benefits include a resolution of preoperative anemia, a decrease in fibroid size, a reduction of endometrial thickness and vascularization with subsequently improved visibility and reduced fluid absorption, and the possibility of surgical scheduling. Conversely, this preoperative treatment is associated with some side effects such as hot flushes and postinjection endometrial bleeding due to the flare-up effect. Data on SPRM showed that eighty percent of patients treated by UPA showed a clinically meaningful reduction of more than 25% in fibroid volume, and 50% of patients a reduction of 50%. In the subpopulation of patients not undergoing surgery, fibroid volume reduction appeared to be maintained for 6 months after the end of UPA treatment. This was in contrast to patients receiving a GnRH agonist, in whom fibroids began to regrow 1 to 3 months after the last dose, reaching their baseline size after 6 months. No sub-analysis have been conducted on submucosal fibroids, but is of interest to underline that, when myomas regress so much that they no longer distort the uterine cavity, surgery may not be required. This could represent a safe way to avoid surgery in patients with G2 fibroids desiring pregnancy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibroid
Keywords
fibroid, GnRH analogue, ulipristal acetate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ulipristal acetate
Arm Type
Experimental
Arm Description
Women will be treated with an oral dose of ulipristal acetate 5 mg/day for 2 courses of 3 months each
Arm Title
Leuprolile acetate
Arm Type
Active Comparator
Arm Description
Women will be treated with an injection IM on leuprolide acetate 11,25 in the luteal phase repeated 3 months later
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 and up to three months later for two courses, with an interval between the courses of 1 month
Intervention Type
Drug
Intervention Name(s)
Leuprolide acetate
Other Intervention Name(s)
Enantone 11.25
Intervention Description
One dose of 11.25 GnRH analogue depot will be administered in the luteal phase of the menstrual cycle (days 21-24) and repeated 3 months later
Primary Outcome Measure Information:
Title
Proportion of restored uterine cavity 1 year after enrollment
Description
To compare the proportion of patients, treated by UPA or by GnRh-a, with uterine cavity no longer distorted by their submucous myoma
Time Frame
1 year after treatment
Secondary Outcome Measure Information:
Title
Time to pregnancy
Description
to compare time to pregnancy in patients treated with Ulipristal Acetate and GnRH-a
Time Frame
from the end of treatment to the obtainance of pregnancy
Title
Live birth rate
Description
to compare live birth rate in patients treated with Ulipristal Acetate and GnRH-a
Time Frame
A the time of delivery
Title
Proportion of patients needing surgery after UPA or GnRH-a
Description
to compare need for surgery in patients treated with Ulipristal Acetate and GnRH-a.
Time Frame
24 weeks after the first dose of drugs

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: G2 submucosal leiomyoma <3 cm, symptoms of menomethrorragia, menstrual disorder, infertility, pelvic pain Exclusion Criteria: submucosal leyomyoma other than G2 or greater than 3 cm, intramural or subserosal leiomyomas endometrial hyperplasia with atypia history of uterine surgery
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
First Name & Middle Initial & Last Name & Degree
Roberta Venturella, MD

12. IPD Sharing Statement

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Ulipristal Acetate Versus GnRH Analogue and Myometrial Preservation

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