Changes in Knee Articular Cartilage Volume in Women on Aromatase Inhibitors

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2009 by Monash University.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Monash University
ClinicalTrials.gov Identifier:
NCT00111241
First received: May 18, 2005
Last updated: September 17, 2009
Last verified: September 2009

May 18, 2005
September 17, 2009
May 2005
May 2010   (final data collection date for primary outcome measure)
Knee cartilage volume [ Time Frame: Two years ] [ Designated as safety issue: No ]
Knee cartilage volume
Complete list of historical versions of study NCT00111241 on ClinicalTrials.gov Archive Site
  • Menopausal symptoms [ Time Frame: Two years ] [ Designated as safety issue: No ]
  • Well-being [ Time Frame: Two years ] [ Designated as safety issue: No ]
  • Menopausal symptoms
  • Well-being
Not Provided
Not Provided
 
Changes in Knee Articular Cartilage Volume in Women on Aromatase Inhibitors
Assessment of Knee Joint Articular Cartilage Volume Change, Bone Loss and Change in Body Composition in Women Treated With Anastrozole or Letrozole and Comparison With Untreated Controls

Many women with breast cancer are treated with a class of drugs called aromatase inhibitors (mainly letrozole or anastrozole), which lowers the amount of estrogen being produced in the body. Women on aromatase inhibitors appear to experience joint pains and arthralgia. The aim of this study is to determine whether the joint pains experienced by some women on aromatase inhibitors is associated with more defects in their cartilage, compared to women not receiving this therapy. Using the magnetic resonance imaging (MRI) technique, the knee joint will be examined to assess changes in cartilage volume over time.

The mechanism of increased bone loss and fracture risk is clearly related to the depletion of estrogen production in the bone. But why there is a higher rate of reporting arthralgia, fracture and joint pain amongst women on aromatase inhibitors is not understood.

Using magnetic resonance imaging (MRI) to measure knee articular cartilage volume, we have demonstrated that post menopausal hormone therapy used for at least five years is associated with retention of articular cartilage in the knee, indicating that oestrogen may protect against the development of osteoarthritis in post menopausal women. Furthermore, we have recently observed that free testosterone is associated with loss of tibial cartilage, after taking into account age, body mass index, baseline tibial cartilage volume, tibial plateau area and total bone mineral content in healthy men. Whether an excess of testosterone to oestrogen as a consequence of aromatase inhibition has an adverse effect on articular cartilage volume warrants further investigation.

This study will include non-hysterectomised women aged 40 to 65 years who have undergone breast surgery and then commenced on aromatase inhibitors within the preceding 12 weeks. The control group (which has been fully recruited) included non-hysterectomised, healthy women aged 40 to 65 years. A MRI of the dominant knee will be used to compare changes in knee articular volume over time. A MRI will be done at baseline and again at 2 years. Changes in knee articular volume is the primary outcome. We will also use this opportunity to compare menopausal symptoms (assessed using the Menopause Quality of Life [MENQOL] questionnaire) between women treated with aromatase inhibitors and those who are not. Well-being will also be assessed using the Psychological General Well-Being index.

Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
Not Provided
Not Provided
Non-Probability Sample

Participants will be informed of study by their treating physician and invited to participate and by community sample.

Arthralgia
Drug: aromatase inhibitors (letrozole, anastrozole)
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
170
December 2010
May 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

Group 1 :

  • Aged 40 - 65
  • Non-hysterectomised women who have undergone breast surgery
  • Women on aromatase inhibitors within preceding 12 weeks

Group 2 : control group

  • Healthy, non-hysterectomised women aged 40-65 .

Exclusion Criteria:

  • Previous knee injury requiring non-weight bearing treatment for > 24 hrs or surgery (including arthroscopy)
  • Inability to complete the study (eg proposed relocation)
  • Contraindication to undergoing an MRI including pacemaker, metal sutures, presence of shrapnel, iron filings in eye
  • Claustrophobia

Additional Exclusions for Group 1

  • Treatment with tamoxifen for > 8 weeks prior to commencement
  • Knee pain lasting for >24 hours in the last 5 years (prior to commencement on anastrozole or letrozole)
  • Anastrazole or Letrozole therapy for > 12 weeks
Female
40 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
Australia
 
NCT00111241
2004/949
Not Provided
Professor Susan Davis, Women's Health Program
Monash University
Not Provided
Principal Investigator: Susan Davis, MBBS FRACP PhD Director Women's Health Program
Monash University
September 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP