ClinicalTrials.Veeva

Menu

Prevalence and Risk Factors for Pain and Related Adverse Reactions Among Breast Cancer Survivors on Aromatase Inhibitors

P

Peking University

Status

Enrolling

Conditions

Breast Cancer
Aromatase Inhibitors
Endocrine Therapy
Depression
Anxiety
Pain
Sleep

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

We obtained the occurrence of pain sensation, pain mood, sleep, etc. during endocrine therapy in breast cancer patients through telephone follow-up, and analyzed risk factors through artificial intelligence

Enrollment

1,200 estimated patients

Sex

Female

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Breast cancer survivors on aromatase inhibitors

Exclusion criteria

  • Advanced breast cancer

Trial design

1,200 participants in 2 patient groups

PAIN
Treatment:
Other: No intervention
NO PAIN
Treatment:
Other: No intervention

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems