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 @ 11:39 PM
Ignite Modification Date: 2025-12-24 @ 11:39 PM
NCT ID: NCT01868451
Eligibility Criteria: Inclusion Criteria: * Histologic diagnosis of classical, CD30 positive Hodgkin lymphoma confirmed at enrolling institution * FDG-avid disease by FDG-PET/CT and measurable disease of at least 1.5 cm by CT * Ann Arbor Stage I or II disease * Disease bulk defined as any lymph node mass with transverse maximal diameter \> 7.0 cm OR coronal maximal diameter \> 7.0 cm on CT imaging * Females of childbearing age must be on an acceptable form of birth control per institutional standards * Ages 18 and over Exclusion Criteria: * Cardiac ejection fraction ≤ 50% * Hemoglobin-adjusted diffusing capacity for carbon monoxide \< 40% * ANC≤1000/μl and Platelets≤75,000/μl * Total bilirubin ≥ 2.0 mg/dl in the absence of a history of Gilbert's disease * Serum creatinine clearance of \<30 mL/min as estimated by the Cockcroft-Gault Method * Known pregnancy or breast-feeding * Known history of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS) * Medical illness unrelated to Hodgkin Lymphoma, which, in the opinion of the attending physician and/or MSKCC principal investigator, makes participation in this study inappropriate. * Peripheral neuropathy \> grade 1 * Patients receiving chronic treatment with systemic steroids. However, patients can receive up to 10 days of steroid therapy prior to starting treatment with BV+AVD.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT01868451
Study Brief:
Protocol Section: NCT01868451