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 @ 11:43 PM
Ignite Modification Date:
2025-12-24 @ 11:43 PM
NCT ID:
NCT01793051
Eligibility Criteria:
Inclusion Criteria:
1. Patients with pathologically diagnosed who have received induction chemotherapy, with or without AuSCT, and who have qualified to receive lenalidomide-based maintenance therapy for their MM.
2. Patients \> or = 18 years old.
3. Patients able to render informed consent and to follow protocol requirements.
4. Patients who speak English (due to patient-reported outcome language options, we are only accruing English-speaking patients to the protocol).
5. Patients with normal renal function according to MD Anderson testing standards and no prior renal disease \[screening cut off for serum creatinine \< 1.5 times the upper limit of normal\].
6. Patients with normal hepatic function according to MD Anderson testing standards and no prior liver disease \[screening results for total bilirubin must be \< 1.5 times the upper limit of normal; screening results for alkaline phosphatase (ALP) and alanine aminotransferase (ALT) must be \< 2 times the upper limit of normal; if available, screening results for aspartate aminotransferase (AST) must be \< 2 times the upper limit of normal\].
Exclusion Criteria:
1. Patients who are taking minocycline for other conditions, as determined by the treating physician
2. Patients with hypersensitivity to tetracyclines
3. Women who are pregnant or nursing; pregnancy will be confirmed by urine test
4. Patients who are enrolled in other clinical trials that have symptom management as primary outcome
5. Patients who are not able to use telephone-based interactive voice response software due to physical limitations (e.g., impaired hearing)
6. Patients taking any tetracycline in the last 15 days
7. Patients on Vitamin K antagonist warfarin
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01793051
Study Brief:
Protocol Section:
NCT01793051