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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Withdrawn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
American University of Beirut Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Symptomatic or Large Uterine Fibroids focused on measuring Leiomyoma, perimenopause, aromatase inhibitor

Eligibility Criteria

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

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:

  1. Women <50 years of age
  2. Postmenopausal women
  3. Women with impaired renal function
  4. Oral treatment with any type of estrogen or progesterone more recently than 1 month
  5. History of venous thromboembolism
  6. 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

First Posted
July 23, 2009
Last Updated
July 12, 2012
Sponsor
American University of Beirut Medical Center
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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Withdrawn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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