CClinicalTrials.gg
Status unknownNCT01431053Updated Mar 13, 2013

Study of Aspirin and Exemestane as Adjuvant Treatment in Breast Cancer

A Phase 2 interventional study of aspirin and Exemestane in Breast Neoplasms, sponsored by Chinese Academy of Medical Sciences. Status unknown at 1 site in China. Open to female participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2013-03-13.

Sponsored by Chinese Academy of Medical Sciences · Phase 2, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Mar 2013), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
160
Allocation
Randomized
Ages
50 Years to 80 Years
Sex
Female
01

Study summary

This is a phase II study to assess efficacy/safety of Exemestane with or without Aspirin as the adjuvant treatment in postmenopausal breast cancer patients.

02

Conditions studied

  • Breast Neoplasms

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Keywords

  • exemestane
  • aspirin
  • quality of life
03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 160 is above the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Chinese Academy of Medical Sciences is the lead sponsor of 235 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 80 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Breast cancer after surgery postmenopausal

Exclusion criteria

Exclusion Criteria:

  • contraindication of aspirin
05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
160 participants (estimated)

Study arms

  • Experimental
    Exemestane + Aspirin

    Drug: aspirin · Drug: Exemestane

  • Active comparator
    Exemestane

    Drug: Exemestane

Interventions

  • Drugaspirin

    Aspirin 50mg po daily

  • DrugExemestane

    Exemestane 25mg po daily

06

What researchers measure

Primary outcomes

  1. Quality of Life

    Time frame: 4 years

07

Study locations

1 of 1 sites recruiting
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences
    Beijing, 100021, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 13, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01431053
Lead sponsor
Chinese Academy of Medical Sciences
Responsible party
Peng Yuan (Associate Chief Physician, Chinese Academy of Medical Sciences) — Principal investigator
First posted
Sep 9, 2011
Start date
Jul 2011
Primary completion
Jul 2014 (estimated)
Completion
Jul 2014 (estimated)
Last update
Mar 13, 2013

Study contacts

Peng Yuan, M.D.
Contact
yuanpeng01@hotmail.com
86-135 0127 0834
Peng Yuan, M.D.
principal investigator · Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2013. You cannot join it, but the record below documents what was studied.

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