Ulipristal Acetate for the Preoperative Management of Hypoechoic Cellular Leiomyomas
Primary Purpose
Fibroid
Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
ulipristal acetate
Leuprolide acetate
Sponsored by
About this trial
This is an interventional treatment trial for Fibroid focused on measuring fibroid, cellular leiomyomas, GnRH analogue, ulipristal acetate
Eligibility Criteria
Inclusion Criteria:
- hypoechoic uterine leiomyoma (echogenicity <3),
- intramural leiomyomas with an ultrasonographic size <20 cm but >4cm,
- indication to surgery (symptoms of menometrorrhagia,
- menstrual disorder,
- infertility,
- pelvic pain or pelvic pressure
Exclusion Criteria:
- submucosal leiomyoma,
- 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 3 months
Women will be treated with an intramuscular (IM) injection of leuprolide acetate 11.25 mg in the luteal phase
Outcomes
Primary Outcome Measures
Operative time (minutes)
To evaluate the difference in terms of operative times in patients with hypoechoic CLs submitted to laparoscopic myomectomy and preoperatively treated by ulipristal acetate or GnRh-a .
Secondary Outcome Measures
Difficulty of leiomyoma enucleation assessed by surgeon on a VAS scale
To compare surgical feasibility (VAS) in patients treated with Ulipristal Acetate and GnRH-a.
Intraoperative blood loss (delta Hb)
To compare blood loss (delta HB) in patients treated with Ulipristal Acetate and GnRH-a.
Post-operative evaluation of leiomyomas characteristics
This is a composite outcome aimed to compare pathological myoma characteristics (cellularity, necrosis, fibrosis) in patients treated with Ulipristal Acetate and GnRH-a.
Full Information
NCT ID
NCT02361905
First Posted
February 2, 2015
Last Updated
November 17, 2016
Sponsor
University Magna Graecia
1. Study Identification
Unique Protocol Identification Number
NCT02361905
Brief Title
Ulipristal Acetate for the Preoperative Management of Hypoechoic Cellular Leiomyomas
Official Title
Advantages of Ulipristal Acetate for the Preoperative Treatment of Hypoechoic Cellular Leiomyomas
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
Cellular leiomyomas (CLs) are described as leiomyomas that are significantly more cellular than the surrounding myometrium, often with crowding and overlapping of nuclei. they often are soft and appear more tan or yellow and less circumscribed than the usual leiomyomas. Pre-operatively CLs can be recognized at ultrasound evaluation because they appear as hypoechoic uterine lesions. patients with hypoechoic myoma have a significantly longer surgery time after treatment with a gonadotropin-releasing hormone (GnRH) analog probably related to degenerative changes induced by this treatment. Hypoechoic CLs should be more responsive to ulipristal acetate treatment than common leiomyomas. The antiproliferative ulipristal effect, moreover, induces a condition of apoptotic necrosis that, compared to GnRH-a myxoid necrosis, probably allows an easier surgical enucleation of the tumor.
Detailed Description
Rationale why study should be conducted: Leiomyomas are the most common benign neoplasm in women; it has been estimated that these tumors occur in at least 25% of all women, which is probably an underestimation, because this figure is based on a select population. They are histologically composed by smooth muscle cells with bland, uniform, cigar-shaped nuclei that are arranged in interlacing bundles, showing little or no mitotic activity. Cellular leiomyomas (CLs) are described as leiomyomas that are significantly more cellular than the surrounding myometrium, often with crowding and overlapping of nuclei.
The presenting symptoms do not differ from those of patients with typical leiomyomas. On gross examination, CLs are more often soft and appear more tan or yellow and less circumscribed than the usual leiomyomas.
Pre-operatively, anyway, CLs can be recognized at ultrasound evaluation because they appear as hypoechoic uterine lesions. It has been demonstrated that patients with hypoechoic myoma have a significantly longer surgery time after treatment with a GnRH analog than for the rest of the pretreated fibroids or the untreated patients with hypoechoic myomas. Considering the predominant relevance of the traction maneuvers in laparoscopic myomectomy, the difficulty in adequately grasping the tumor is the key element in the longer operative time. The greater softening of the fibroid tissue is probably related to degenerative changes induced by the GnRH-analog pretreatment, particularly in those fibroids without an adequate fibrous "skeleton" and thus with the appearance as hypoechoic at the admission ultrasonography. From a pathologic point of view, these fibroids, when pretreated, showed a predominance of areas of coagulative necrosis and mixoid degeneration, causing longer operative time and showing unequivocally the negative effect of preoperative GnRH analog treatment for these kinds of uterine fibroids.
At the same time, hypoechoic CLs should be more responsive to ulipristal acetate treatment than common leiomyomas, given its antiproliferative activity in cultured leiomyoma cells.
The antiproliferative ulipristal effect, moreover, induces a condition of apoptotic necrosis that, compared to GnRH-a myxoid necrosis, probably allows an easier surgical enucleation of the tumor.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibroid
Keywords
fibroid, cellular leiomyomas, 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
42 (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 3 months
Arm Title
Leuprolile acetate
Arm Type
Active Comparator
Arm Description
Women will be treated with an intramuscular (IM) injection of leuprolide acetate 11.25 mg in the luteal phase
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
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)
Primary Outcome Measure Information:
Title
Operative time (minutes)
Description
To evaluate the difference in terms of operative times in patients with hypoechoic CLs submitted to laparoscopic myomectomy and preoperatively treated by ulipristal acetate or GnRh-a .
Time Frame
At the time of skin closure at the end of the myomectomy
Secondary Outcome Measure Information:
Title
Difficulty of leiomyoma enucleation assessed by surgeon on a VAS scale
Description
To compare surgical feasibility (VAS) in patients treated with Ulipristal Acetate and GnRH-a.
Time Frame
Within 2 hours after the end of the myomectomy
Title
Intraoperative blood loss (delta Hb)
Description
To compare blood loss (delta HB) in patients treated with Ulipristal Acetate and GnRH-a.
Time Frame
The day before surgery and 3 hours after the myomectomy
Title
Post-operative evaluation of leiomyomas characteristics
Description
This is a composite outcome aimed to compare pathological myoma characteristics (cellularity, necrosis, fibrosis) in patients treated with Ulipristal Acetate and GnRH-a.
Time Frame
At the time of pathological assessment
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
hypoechoic uterine leiomyoma (echogenicity <3),
intramural leiomyomas with an ultrasonographic size <20 cm but >4cm,
indication to surgery (symptoms of menometrorrhagia,
menstrual disorder,
infertility,
pelvic pain or pelvic pressure
Exclusion Criteria:
submucosal leiomyoma,
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
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
Learn more about this trial
Ulipristal Acetate for the Preoperative Management of Hypoechoic Cellular Leiomyomas
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