Aromatase Inhibitors for Treatment of Uterine Leiomyomas
Primary Purpose
Symptomatic or Large Uterine Fibroids
Status
Withdrawn
Phase
Phase 1
Locations
Lebanon
Study Type
Interventional
Intervention
Letrozole (aromatase inhibitor)
Sponsored by
About this trial
This is an interventional treatment trial for Symptomatic or Large Uterine Fibroids focused on measuring Leiomyoma, perimenopause, aromatase inhibitor
Eligibility Criteria
Inclusion Criteria:
1. Perimenopausal women (≥ 50 years) with symptomatic uterine leiomyomas (menometrorrhagia, pressure symptoms, urinary retention, pelvic pain) or those with large leiomyomas ≥ 7 cms
Exclusion Criteria:
- Women <50 years of age
- Postmenopausal women
- Women with impaired renal function
- Oral treatment with any type of estrogen or progesterone more recently than 1 month
- History of venous thromboembolism
- Any contraindication for Magnetic Resonance Imaging (MRI)
Sites / Locations
- American University of Beirut
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
aromatase inhibitors: Letrozole
Arm Description
All consenting patients will be started on Letrozole at a dose of 2.5 mg/day for 8 weeks.
Outcomes
Primary Outcome Measures
The primary end point of this study will be the baseline to end point percent difference in leiomyoma volume at 2 months and 6 months following treatment with Letrozole.
Secondary Outcome Measures
Improvement in symptoms
Need for a surgical intervention
Improvement in the hemoglobin levels
Development of side effects: hot flushes, nausea,vomiting, headache, thrombophlebitis
Full Information
NCT ID
NCT00945360
First Posted
July 23, 2009
Last Updated
July 12, 2012
Sponsor
American University of Beirut Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT00945360
Brief Title
Aromatase Inhibitors for Treatment of Uterine Leiomyomas
Official Title
Aromatase Inhibitors for the Prevention of the Growth of Uterine Leiomyomas in Perimenopausal Women: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2009
Overall Recruitment Status
Withdrawn
Why Stopped
Inability to recruit patients
Study Start Date
March 2011 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2011 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
American University of Beirut Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Fibroids are benign tumors that might results in bleeding. Surgery is their definitive treatment. Some medical therapies have been tried for women who wish to preserve their uterus. Recent reports have demonstrated a role for a new category of drugs called aromatase inhibitor (such as Femara) in the treatment of fibroids. This study is conducted to assess the effect of Femara (letrozole) on the size of fibroids in women around menopause.
Detailed Description
Fibroids (leiomyomas) are benign tumors that originate in the musculature of the uterus. They are the most common cause for removal of the uterus in women. Surgery is the final definitive treatment of fibroids. However, surgery is relatively risky. Hence, a few medical therapies have been tried for women who wish to preserve their uterus. However, most of those therapies have side effects that prohibit their routine use. Recent reports have demonstrated a role for a new category of drugs called aromatase inhibitor ( such as Femara) in the treatment of fibroids. To the best of our knowledge, this drug has not been studied yet in the management of fibroid of the uterus apart from one case report.
The objective of the current study is to assess the effect of aromatase inhibitors, specifically Femara (letrozole) on the size of fibroids in women around menopause. We are hoping that by decreasing their size, we could avoid having patients undergo surgery. The data generated is invaluable in that sense.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Symptomatic or Large Uterine Fibroids
Keywords
Leiomyoma, perimenopause, aromatase inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
aromatase inhibitors: Letrozole
Arm Type
Experimental
Arm Description
All consenting patients will be started on Letrozole at a dose of 2.5 mg/day for 8 weeks.
Intervention Type
Drug
Intervention Name(s)
Letrozole (aromatase inhibitor)
Other Intervention Name(s)
Letrozole
Intervention Description
Letrozole at a dose of 2.5 mg/day for 8 weeks.
Primary Outcome Measure Information:
Title
The primary end point of this study will be the baseline to end point percent difference in leiomyoma volume at 2 months and 6 months following treatment with Letrozole.
Time Frame
2 months and 6 months following treatment
Secondary Outcome Measure Information:
Title
Improvement in symptoms
Time Frame
2 and 6 months following treatment
Title
Need for a surgical intervention
Time Frame
2 and 6 months following treatment
Title
Improvement in the hemoglobin levels
Time Frame
2 and 6 months following treatment
Title
Development of side effects: hot flushes, nausea,vomiting, headache, thrombophlebitis
Time Frame
2 and 6 months following treatment
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1. Perimenopausal women (≥ 50 years) with symptomatic uterine leiomyomas (menometrorrhagia, pressure symptoms, urinary retention, pelvic pain) or those with large leiomyomas ≥ 7 cms
Exclusion Criteria:
Women <50 years of age
Postmenopausal women
Women with impaired renal function
Oral treatment with any type of estrogen or progesterone more recently than 1 month
History of venous thromboembolism
Any contraindication for Magnetic Resonance Imaging (MRI)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anwar H Nassar, MD
Organizational Affiliation
American University of Beirut Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
American University of Beirut
City
Beirut
Country
Lebanon
12. IPD Sharing Statement
Learn more about this trial
Aromatase Inhibitors for Treatment of Uterine Leiomyomas
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