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Advanced Breast CancerNCT01311037

The Combination of GnRh Analogue and Aromatase Inhibitor in Receptor Positive Premenopausal Women With Advanced Breast Cancer

An observational study of Advanced Breast Cancer, run by King Faisal Specialist Hospital & Research Center at 1 site in Saudi Arabia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The Combination of GnRh Analogue and Aromatase Inhibitor in Receptor Positive Premenopausal Women with Advanced Breast Cancer A Prospective Trial. Read more about this study

Who is it for?
Ages 45 to 85 years, women only
Conditions the study is for
Advanced Breast Cancer
What is being tested?
GnRh Analogue and Aromatase Inhibitor
How many people
2 participants
Where
1 siteSaudi Arabia
Study dates
Jan 2009to not given
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 85 years
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: Receptor Positive Premenopausal Women with Advanced Breast Cancer.

Who may be able to join

  • Receptor Positive Premenopausal Women with Advanced Breast Cancer.

Who cannot join

  • Any woman other than diagnosis of Receptor Positive Premenopausal with Advanced Breast Cancer.

Trial locations and contacts

1 site in 1 country.

Al Sayed, M.D. contact

+966-1-4423949

Saudi Arabia1 site, 1 recruiting
  • Kfsh & Rc

    Riyadh

    Recruiting

Other trials in Saudi Arabia

About this study

Official title: The Combination of GnRh Analogue and Aromatase Inhibitor in Receptor Positive Premenopausal Women With Advanced Breast Cancer A Prospective Trial

The Combination of GnRh Analogue and Aromatase Inhibitor in Receptor Positive Premenopausal Women with Advanced Breast Cancer A Prospective Trial.

Read the detailed description

The Combination of GnRh Analogue and Aromatase Inhibitor in Receptor Positive Premenopausal Women with Advanced Breast Cancer A Prospective Trial.

Being tested
GnRh Analogue and Aromatase Inhibitor
Keywords
Premenopausal Women with Advanced Breast Cancer

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GnRh Analogue and Aromatase InhibitorOther

    GnRh Analogue and Aromatase Inhibitor

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Mar 2011 (estimated)
  2. Study startJan 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
2 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01311037
Sponsor's protocol ID
RAC# 2081-064
Other IDs
RAC# 2081-064
Status last verified
Dec 2011
First submitted
6 Mar 2011
Last updated
13 Dec 2011
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Advanced Breast Cancer, run by King Faisal Specialist Hospital & Research Center at 1 site in Saudi Arabia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 13 Dec 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Al Sayed, M.D. (+966-1-4423949), or a site near the patient. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Dec 2011.

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