Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 9:15 PM
Ignite Modification Date: 2025-12-24 @ 9:15 PM
NCT ID: NCT00383604
Eligibility Criteria: Inclusion Criteria: * Patients enrolled in the proposed studies must be survivors of breast cancer at a time point at least 4 years following the initial surgery and radiotherapy for the disease. * Patients must have a history of unilateral axillary lymph node dissection. * Patients referred to, or that receive their care within the Stanford University Breast Cancer Program and the Stanford Center for Lymphatic and Venous Disorders. * Patients will be required to have the capacity to provide informed consent. Exclusion Criteria: * Patients with other serious systemic illness (renal failure, hepatic dysfunction, congestive heart failure, neurological or psychological impairment) that would confound the study or impair the patients' ability to participate. * Patients will not be enrolled if they are taking drugs that affect carbohydrate metabolism. * Patients with recurrent breast cancer or other forms of pre-existing lymphedema will be ineligible.
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 18 Years
Study: NCT00383604
Study Brief:
Protocol Section: NCT00383604