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Ulipristal vs. GnRHa Prior to Laparoscopic Myomectomy (MYOMEX)

Primary Purpose

Fibroids

Status
Unknown status
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
GnRHa
Ulipristal
Sponsored by
Amsterdam UMC, location VUmc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibroids

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

Women visiting the gynecological outpatient department with symptomatic fibroids will be screened for eligibility. In order to be eligible to participate in this trial, a subject must meet all of the following criteria:

  • provide written consent prior to any study related procedures
  • pre-menopausal
  • a planned resection of a maximum of 2 FIGO (PALM-COEIN classification) type 3, 4, 5, 6 or 2-5 fibroids of >5 cm
  • the(se) fibroid(s) should be between 5 and 12 cm (maximum diameter)
  • other fibroids should be small (<2 cm), not clinically relevant, or not resectable (e.g. difficult position), or type 7 (any size)
  • eligible for laparoscopic myomectomy

Exclusion Criteria:

A potential subject who meets any of the following criteria will be excluded from participation in this trial:

  • Current pregnancy
  • (suspicion of) malignancy
  • any type 0-2 fibroids smaller than 5 cm
  • more than 2 type 3-6 fibroids > 5 cm that need to be removed (except type 7 fibroids of any size)
  • use of any hormonal agents and not willing to discontinue their use
  • use of anticoagulants
  • coagulopathy
  • Use of NSAIDs impacting bleeding before surgery
  • Contraindication to laparoscopy procedure or causes of complications (multiple laparotomies, frozen pelvis, severe endometriosis)
  • allergy to leuprolide acetate/comparable nonapeptides or Ulipristal

Sites / Locations

  • FlevoziekenhuisRecruiting
  • Onze Lieve Vrouwen GasthuisRecruiting
  • Sint Lucas Andreas ZiekenhuisRecruiting
  • VU medical centerRecruiting
  • Catharina ZiekenhuisRecruiting
  • Spaarne GasthuisRecruiting
  • Radboud University Medical CenterRecruiting
  • Maasstad ziekenhuisRecruiting
  • Maxima Medisch CentrumRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

GnRHa and placebo tablets

Ulipristal

Control

Arm Description

11.25 mg Leuproreline injections at the onset of pretreatment with placebo tablets (once daily)

Three months of Ulipristal 5 mg once daily combined with a single saline injection at the onset of pretreatment (produced as placebo of Leuproreline)

No pre-treatment prior to laparoscopic myomectomy

Outcomes

Primary Outcome Measures

Blood loss during surgery
Ulipristal is non-inferior to GnRHa in terms of blood loss during surgery when the average difference between the two groups is below 150 ml (standard deviation 250 ml)

Secondary Outcome Measures

Full Information

First Posted
November 6, 2014
Last Updated
November 2, 2016
Sponsor
Amsterdam UMC, location VUmc
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1. Study Identification

Unique Protocol Identification Number
NCT02288130
Brief Title
Ulipristal vs. GnRHa Prior to Laparoscopic Myomectomy
Acronym
MYOMEX
Official Title
Ulipristal Versus Gonadotropin-releasing Hormone Agonists Prior to Laparoscopic Myomectomy: a Double Blind Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
December 2014 (undefined)
Primary Completion Date
July 2017 (Anticipated)
Study Completion Date
November 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Amsterdam UMC, location VUmc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rationale: Laparoscopic myomectomy is increasingly performed over laparotomic myomectomy, because of the many benefits for the patient in terms of pain, hospital stay and recovery. In order to increase the success rate of a laparoscopic procedure pre-treatment to decrease the volume might be beneficial. Gonadotropin-releasing hormone agonists (GnRHa) are used for this purpose with good results in terms of volume reduction, but sometimes resulting in loss of distinction of the right surgical planes. Ulipristal is a new pre-operative treatment option for symptomatic fibroids, which has demonstrated good results in terms of volume reduction. The effect on cleavage planes is unknown. This study is performed to evaluate if Ulipristal is as effective as GnRHa in terms of surgical outcome. Objective: to investigate if Ulipristal is non-inferior to GnRH in terms of intra-operative blood-loss (primary outcome), surgical time, surgical ease, complications, quality of life and costs. Study design: Double blind randomized controlled multi-center trial. Study population: Premenopausal women in whom a maximum of 2 symptomatic intramural fibroids between 5 and 12 cm in diameter will be removed. Fibroid types 3, 4, 5, 6 and 2-5 will be included. Intervention: Three months of Ulipristal 5 mg once daily combined with a single saline injection at the onset of pretreatment (produced as placebo of Leuproreline) or (comparison) 11.25 mg Leuproreline injections at the onset of pretreatment with placebo tablets (once daily) . Methods: Within 1 month after pre-treatment patients will undergo a laparoscopic myomectomy by experienced surgeons. Operative characteristics will be recorded prospectively. Follow up will be 6 months after surgery mainly for quality of life assessment. A cost utility analysis will be conducted alongside the trial. Main study parameters/endpoints: Ulipristal is non-inferior to GnRHa in terms of blood loss during surgery when the average difference between the two groups is below 150 ml (standard deviation 250 ml). Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Both Ulipristal and GnRHa have been registered for this indication. Safety has been tested and no specific risks apply.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibroids

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GnRHa and placebo tablets
Arm Type
Active Comparator
Arm Description
11.25 mg Leuproreline injections at the onset of pretreatment with placebo tablets (once daily)
Arm Title
Ulipristal
Arm Type
Active Comparator
Arm Description
Three months of Ulipristal 5 mg once daily combined with a single saline injection at the onset of pretreatment (produced as placebo of Leuproreline)
Arm Title
Control
Arm Type
No Intervention
Arm Description
No pre-treatment prior to laparoscopic myomectomy
Intervention Type
Drug
Intervention Name(s)
GnRHa
Other Intervention Name(s)
Lucrin
Intervention Type
Drug
Intervention Name(s)
Ulipristal
Other Intervention Name(s)
Esmya
Primary Outcome Measure Information:
Title
Blood loss during surgery
Description
Ulipristal is non-inferior to GnRHa in terms of blood loss during surgery when the average difference between the two groups is below 150 ml (standard deviation 250 ml)
Time Frame
Reported directly after surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women visiting the gynecological outpatient department with symptomatic fibroids will be screened for eligibility. In order to be eligible to participate in this trial, a subject must meet all of the following criteria: provide written consent prior to any study related procedures pre-menopausal a planned resection of a maximum of 2 FIGO (PALM-COEIN classification) type 3, 4, 5, 6 or 2-5 fibroids of >5 cm the(se) fibroid(s) should be between 5 and 12 cm (maximum diameter) other fibroids should be small (<2 cm), not clinically relevant, or not resectable (e.g. difficult position), or type 7 (any size) eligible for laparoscopic myomectomy Exclusion Criteria: A potential subject who meets any of the following criteria will be excluded from participation in this trial: Current pregnancy (suspicion of) malignancy any type 0-2 fibroids smaller than 5 cm more than 2 type 3-6 fibroids > 5 cm that need to be removed (except type 7 fibroids of any size) use of any hormonal agents and not willing to discontinue their use use of anticoagulants coagulopathy Use of NSAIDs impacting bleeding before surgery Contraindication to laparoscopy procedure or causes of complications (multiple laparotomies, frozen pelvis, severe endometriosis) allergy to leuprolide acetate/comparable nonapeptides or Ulipristal
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Inge de Milliano, MD
Phone
+31624992776
Email
i.demilliano@vumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wouter Hehenkamp, PhD
Organizational Affiliation
Amsterdam UMC, location VUmc
Official's Role
Study Chair
Facility Information:
Facility Name
Flevoziekenhuis
City
Almere
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marchien van Baal
Facility Name
Onze Lieve Vrouwen Gasthuis
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
P Van Kesteren
Facility Name
Sint Lucas Andreas Ziekenhuis
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreas Thurkow
Facility Name
VU medical center
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wouter Hehenkamp, PhD
Phone
+31204444444
Email
w.hehenkamp@vumc.nl
Facility Name
Catharina Ziekenhuis
City
Eindhoven
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
D Schoot
Facility Name
Spaarne Gasthuis
City
Haarlem
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonas van de Lande
Facility Name
Radboud University Medical Center
City
Nijmegen
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sjors Coppus
Facility Name
Maasstad ziekenhuis
City
Rotterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M Aktas
Facility Name
Maxima Medisch Centrum
City
Veldhoven
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M Bongers

12. IPD Sharing Statement

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Ulipristal vs. GnRHa Prior to Laparoscopic Myomectomy

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