NCT05294367 Dietary and Topical Magnesium Replacement or Supplementation in Patients With Lymphoma
| NCT ID | NCT05294367 |
| Status | Recruiting |
| Phase | EARLY_Phase 1 |
| Sponsor | Mayo Clinic |
| Condition | Lymphoma |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2022-04-15 |
| Primary Completion | 2027-04-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.
This trial targets 60 participants in total. It began in 2022-04-15 with a primary completion date of 2027-04-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This early phase I trial investigates the effect of dietary and topical magnesium replacement on magnesium blood levels in patients with lymphoma. Magnesium is an element in the body that is important to cell health. The body cannot make magnesium and it typically comes from the food we eat. In patients who are ill, magnesium is often replaced intravenously (IV) through a vein or by mouth. This study may help researchers find out if being on a magnesium rich diet and using a magnesium lotion on the skin helps to keep magnesium blood levels in an ideal range. This study also investigates side effects and quality of life when receiving different forms of magnesium.
Eligibility Criteria
Inclusion Criteria: PRE-REGISTRATION - INCLUSION CRITERIA: * Age \>= 18 years * Currently have or have had in the past the diagnosis of any type of lymphoma * If previously treated, the patient must be off myelosuppressive chemotherapy with no planned chemotherapy for \>= 2 months. Patients with lymphoproliferative disorders being observed (i.e., never treated) or those on rituximab (or equivalent) maintenance or chronic oral therapies such as BTK inhibitors, venetoclax, tazemetostat, or corticosteroids are also eligible * Able to eat a full range of solid food and liquids and tolerate seeds/nuts * Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0, 1, or 2 * Provide written informed consent * Able to recollect dietary intake for the prior 24 hours in order to complete a one-day food record with assistance from a dietitian at each study visit * Willing to be seen at the enrolling institution at baseline, and at 4 weeks and 8 weeks (end of treatment) in person or by video/phone * Willing to have a blood magnesium checked every 2 weeks x 4 at any Mayo Clinic site * Ability to complete questionnaire(s) by themselves or with assistance REGISTRATION - INCLUSION CRITERIA: * Magnesium level of 1.5 - 1.9 mg/dL (obtained =\< 5 days prior to registration) Exclusion Criteria: PRE-REGISTRATION - EXCLUSION CRITERIA: * Cannot eat normal table food by mouth. NOTE: Patients with any form of feeding tube or a swallowing disorder are not eligible * Have taken dedicated magnesium supplements (i.e. magnesium oxide) or intravenous (IV) magnesium =\< 28 days prior to pre-registration. Note: If patient is already on a multivitamin containing -magnesium, they may be enrolled, but the brand should not be changed during the 8 weeks on study * Co-morbid systemic illnesses such as active infection or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens * Patients with significant gut malabsorptive conditions (such as inflammatory bowel disease or others at the discretion of the investigator) will be excluded as well as patients with chronic kidney disease stage 3b or greater (estimated glomerular filtration rate \[eGFR\] \< 45) * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements * Receiving any other investigational agent for lymphoma or any other disease * Active other malignancy requiring treatment that would interfere with the assessments of this study * Major surgery other than diagnostic surgery =\< 4 weeks prior to pre-registration * Have an allergy to nuts * Patients with active skin lymphoma or rashes that would preclude lotion testing * Have taken antibiotics =\< 7 days prior to pre-registration
Contact & Investigator
Thomas E. Witzig, M.D.
PRINCIPAL INVESTIGATOR
Mayo Clinic in Rochester
Frequently Asked Questions
Who can join the NCT05294367 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Lymphoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
What phase is the NCT05294367 trial and what does that mean for participants?
Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.
Is NCT05294367 currently recruiting?
Yes, NCT05294367 is actively recruiting participants. Contact the research team at mayocliniccancerstudies@mayo.edu for enrollment information.
Where is the NCT05294367 trial being conducted?
This trial is being conducted at Rochester, United States.
Who is sponsoring the NCT05294367 clinical trial?
NCT05294367 is sponsored by Mayo Clinic. The principal investigator is Thomas E. Witzig, M.D. at Mayo Clinic in Rochester. The trial plans to enroll 60 participants.