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Study of the Efficacy of Dienogest in the Treatment of Uterine Leiomyomas When Compared to Desogestrel and Goserelin

Primary Purpose

Uterine Leiomyoma

Status
Terminated
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Dienogest
Goserelin
Desogestrel
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Uterine Leiomyoma

Eligibility Criteria

35 Years - 55 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women with 35 - 55 years of age
  • Uterine volume between 50cc and 500cc
  • Abnormal uterine bleeding probably associated to intramural uterine leiomyomas

Exclusion Criteria:

  • Pregnancy
  • Liver or kidney dysfunction
  • Women with only submucosal or subserosal uterine leiomyomas
  • Women with contraindications to any of the drugs (categories 3 and 4 of WHO eligibility criteria)
  • Use of anticoagulants
  • Others causes of abnormal uterine bleeding (endometrial pathology, cervical pathology)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Active Comparator

    Arm Label

    Dienogest

    Goserelin

    Desogestrel

    Arm Description

    Dienogest 2mg pills daily during 6 months

    Goserelin 10.8mg preloaded syringe subcutaneously at the start of the study and after 3 months

    Desogestrel 75mcg pills daily during six months

    Outcomes

    Primary Outcome Measures

    Leiomyoma Volume

    Secondary Outcome Measures

    Pictorial Blood Assessment Chart (PBAC) Score Reduction
    Number of episodes of vaginal bleeding

    Full Information

    First Posted
    November 23, 2012
    Last Updated
    August 11, 2020
    Sponsor
    University of Sao Paulo
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01738724
    Brief Title
    Study of the Efficacy of Dienogest in the Treatment of Uterine Leiomyomas When Compared to Desogestrel and Goserelin
    Official Title
    Abnormal Uterine Bleeding in Women With Uterine Leiomyomas: Open Randomized Clinical Trial Of Non Inferiority Between Oral Dienogest, Oral Desogestrel and Subcutaneous Goserelin
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2020
    Overall Recruitment Status
    Terminated
    Why Stopped
    PI went for a post-doc course and when he came back he moved for another job
    Study Start Date
    January 2012 (Actual)
    Primary Completion Date
    December 2016 (Actual)
    Study Completion Date
    December 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Sao Paulo

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The investigators´aim is to assess whether the progestagen dienogest reduces leiomyoma volume and its associated symptoms to the same extent as gonadotropin releasing hormone (GnRH) analogs or the progestagen desogestrel or whether it is inferior to other drugs already in use.
    Detailed Description
    Uterine leiomyoma is a very prevalent condition among women and, although it is mainly asymptomatic, it may be related to bothersome or debilitating symptoms, such as uterine bleeding and pelvic pain or pressure. The standard treatment is surgical (hysterectomy or myomectomy), but there has been continued interest on medical treatments. Progestagens have long been used to control bleeding associated to leiomyomas, but they have not been able to decrease myoma volume. GnRH analogs are well stablished agents, capable of controlling symptoms and decreasing the tumors´volume, but their use is limited by bone loss and menopausal symptoms. A newly introduced progestagen, dienogest, has been studied to treat endometriosis, but its effects on leiomyoma are only starting to be assessed. The investigators are aiming to compare dienogest with the GnRH analog goserelin and the progestagen desogestrel in a randomized trial to see how this new treatment compares with previously used drugs and whether it is similar, inferior or superior to them on controlling leiomyoma associated symptoms and decreasing leiomyoma volume.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    14 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Dienogest
    Arm Type
    Experimental
    Arm Description
    Dienogest 2mg pills daily during 6 months
    Arm Title
    Goserelin
    Arm Type
    Experimental
    Arm Description
    Goserelin 10.8mg preloaded syringe subcutaneously at the start of the study and after 3 months
    Arm Title
    Desogestrel
    Arm Type
    Active Comparator
    Arm Description
    Desogestrel 75mcg pills daily during six months
    Intervention Type
    Drug
    Intervention Name(s)
    Dienogest
    Other Intervention Name(s)
    Allurene, Visanne
    Intervention Description
    Dienogest 2mg pills daily during 6 months
    Intervention Type
    Drug
    Intervention Name(s)
    Goserelin
    Other Intervention Name(s)
    Zoladex
    Intervention Description
    Goserelin 10.8mg preloaded syringe subcutaneously at the start of the study and after 3 months
    Intervention Type
    Drug
    Intervention Name(s)
    Desogestrel
    Other Intervention Name(s)
    Cerazette
    Intervention Description
    Desogestrel 75mcg pills daily during six months
    Primary Outcome Measure Information:
    Title
    Leiomyoma Volume
    Time Frame
    After 6 months of medical therapy
    Secondary Outcome Measure Information:
    Title
    Pictorial Blood Assessment Chart (PBAC) Score Reduction
    Time Frame
    After 6 months of medical therapy
    Title
    Number of episodes of vaginal bleeding
    Time Frame
    After 6 months of medical therapy

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    35 Years
    Maximum Age & Unit of Time
    55 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Women with 35 - 55 years of age Uterine volume between 50cc and 500cc Abnormal uterine bleeding probably associated to intramural uterine leiomyomas Exclusion Criteria: Pregnancy Liver or kidney dysfunction Women with only submucosal or subserosal uterine leiomyomas Women with contraindications to any of the drugs (categories 3 and 4 of WHO eligibility criteria) Use of anticoagulants Others causes of abnormal uterine bleeding (endometrial pathology, cervical pathology)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Luiz Gustavo O Brito, MD, PhD
    Organizational Affiliation
    FMRP-USP
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    Study of the Efficacy of Dienogest in the Treatment of Uterine Leiomyomas When Compared to Desogestrel and Goserelin

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