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Recruiting NCT04829136

NCT04829136 Sustained Oral Fiber Supplementation for Patients Undergoing Donor Stem Cell Transplantation for Hematological Malignancies

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Clinical Trial Summary
NCT ID NCT04829136
Status Recruiting
Phase
Sponsor Fred Hutchinson Cancer Center
Condition Hematopoietic and Lymphatic System Neoplasm
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2022-06-22
Primary Completion 2027-07-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Kate Farms 1.0Standard of Care Nutritional SupportSurvey Administration

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2022-06-22 with a primary completion date of 2027-07-31.

⚠ 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 clinical trial examines sustained oral fiber supplementation for patients undergoing donor stem cell transplantation for hematological malignancies. Patients undergoing donor stem cell transplantation often develop oral and gastrointestinal damage from chemotherapy, radiotherapy, or graft-versus-host disease. Oral fiber nutrition support may improve overall nutrition, support a normal gut microbiome (bacteria that live in the gut) and/or improve gut function in patients undergoing stem cell transplants.

Eligibility Criteria

Inclusion Criteria: * Able to provide written informed consent prior to initiation of any study procedures * Planned allogeneic stem cell transplantation * At least 18 years of age Exclusion Criteria: * Major psychiatric diagnosis that impairs cognitive functioning or is not controlled at the time of the approach, as judged by the patient's medical team * Pregnant or breastfeeding. Pregnancy test is obtained as part of pre-transplant evaluation in women of child-bearing potential at arrival to transplant and again within 7 days of conditioning and will be confirmed as negative by review of the chart

Contact & Investigator

Central Contact

David Fredricks

✉ dfredric@fredhutch.org

📞 206-667-1935

Principal Investigator

David Fredricks

PRINCIPAL INVESTIGATOR

Fred Hutch/University of Washington Cancer Consortium

Frequently Asked Questions

Who can join the NCT04829136 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Hematopoietic and Lymphatic System Neoplasm. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04829136 currently recruiting?

Yes, NCT04829136 is actively recruiting participants. Contact the research team at dfredric@fredhutch.org for enrollment information.

Where is the NCT04829136 trial being conducted?

This trial is being conducted at Seattle, United States.

Who is sponsoring the NCT04829136 clinical trial?

NCT04829136 is sponsored by Fred Hutchinson Cancer Center. The principal investigator is David Fredricks at Fred Hutch/University of Washington Cancer Consortium. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology