Ulipristal Acetate Versus GnRH Analogue Treatment Before Hysteroscopic Resection of Uterine Leiomyoma
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 fibroids, gnrh analogue, ulipristal acetate, hysteroscopy
Eligibility Criteria
Inclusion Criteria: submucosal leiomyoma, symptoms of menomethrorragia, menstrual disorder, infertility, pelvic pain.
Exclusion Criteria: 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
Womens will be treated with 5 mg/day of oral ulipristal acetate for 3 months
women will be treated with 1 IM injection of leuprolide acetate 11,25 mg in in the luteal phase
Outcomes
Primary Outcome Measures
Uterine bleeding assessed by pictorial blood-loss assessment chart (PBAC)
To compare the proportion of controlled uterine bleeding in patients with submucous myoma preoperatively treated by ulipristal acetate or by GnRh-a
Secondary Outcome Measures
Feasibility of myoma hysteroscopic resection (VAS score)
Surgeon experience about the hysteroscopy
Operative time
It will be expressed in minutes
Haemoglobin concentration
It will be expressed in mg/dL
Fluid absorption
It will be expressed in mL
Full Information
NCT ID
NCT02361879
First Posted
February 2, 2015
Last Updated
November 17, 2016
Sponsor
University Magna Graecia
1. Study Identification
Unique Protocol Identification Number
NCT02361879
Brief Title
Ulipristal Acetate Versus GnRH Analogue Treatment Before Hysteroscopic Resection of Uterine Leiomyoma
Official Title
Ulipristal Acetate Versus GnRH Analogue Treatment Before Hysteroscopic Resection of Uterine Leiomyoma
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
The uterine leiomyoma is the most common female benign disease. Submucosal fibroid are about 10%, they distort the endometrial cavity causing heavy and/or irregular bleeding (AUB) and infertility. Hysteroscopic removal of submucosal myomas improves this conditions. GnRH analogues are commonly used before hysteroscopic myomectomy to make surgery easier and safer, but they are expensive, have potential side effects and lack a robust evidence base to support this practice. Ulipristal acetate treatment was able and faster to control in 90% of cases uterine bleeding associated with fibroids than GnRH agonists. UPA significantly improved quality of life and pain reduction.
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. Submucosal fibroid are about 10% of all uterine myoma; they distort the endometrial cavity causing heavy and/or irregular bleeding (AUB) and infertility. According to the degree of myometrial penetration, the European Society for Gynaecological Endoscopy (ESGE) classified submucosal myomas in Type 0 (totally intracavitary fibroids), Type I (<50% myometral penetration), or Type II (>50% myometral penetration).
Hysteroscopic removal of submucosal myomas improves menorrhagia and AUB. GnRH analogues are commonly used before hysteroscopic myomectomy to make surgery easier and safer, but they are expensive, have potential side effects and lack a robust evidence base to support this practice. A recent meta-analysis of data demonstrated that symptomatic relief in patients undergoing surgery was similar either following pre-operative GnRH-a administration or without GnRH-a administration, mainly due to the persistence of abnormal bleeding due to the protrusion of the myoma into the uterine cavity.
In recent studies, Ulipristal acetate treatment was able to control uterine bleeding associated with fibroids in more than 90% of cases. Moreover, it controlled bleeding faster than GnRH agonists, with median times to amenorrhea of 5-7 days in patients receiving UPA compared to 21 days in patients receiving a GnRH agonist. It was demonstrated that UPA significantly improved also quality of life. Pain, as measured by the visual analogue scale, showed a degree of relief similar to that achieved for postoperative pain with narcotic and non-narcotic analgesics. This pain reduction is related to the high amenorrhea rate during treatment (severe bleeding being responsible for uterine contractions and prostaglandin secretion). No sub-analysis have been conducted on submucosal fibroids but, according to our experience, this subgroup of myomas may be the one who most benefits from the administration of UPA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibroid
Keywords
fibroids, gnrh analogue, ulipristal acetate, hysteroscopy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
146 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ulipristal acetate
Arm Type
Experimental
Arm Description
Womens will be treated with 5 mg/day of oral ulipristal acetate for 3 months
Arm Title
Leuprolile acetate
Arm Type
Active Comparator
Arm Description
women will be treated with 1 IM injection of leuprolide acetate 11,25 mg in 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
Uterine bleeding assessed by pictorial blood-loss assessment chart (PBAC)
Description
To compare the proportion of controlled uterine bleeding in patients with submucous myoma preoperatively treated by ulipristal acetate or by GnRh-a
Time Frame
90 days after the beginning of the treatment
Secondary Outcome Measure Information:
Title
Feasibility of myoma hysteroscopic resection (VAS score)
Description
Surgeon experience about the hysteroscopy
Time Frame
Within 2 hours after the end of the hysteroscopy
Title
Operative time
Description
It will be expressed in minutes
Time Frame
Within 2 hours after the end of the hysteroscopy
Title
Haemoglobin concentration
Description
It will be expressed in mg/dL
Time Frame
The day before and 3 hours after the hysteroscopy
Title
Fluid absorption
Description
It will be expressed in mL
Time Frame
Within 2 hours after the end of the hysteroscopy
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: submucosal leiomyoma, symptoms of menomethrorragia, menstrual disorder, infertility, pelvic pain.
Exclusion Criteria: 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, MD,PhD
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 Versus GnRH Analogue Treatment Before Hysteroscopic Resection of Uterine Leiomyoma
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