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Trial record 5 of 15 for:    gluten | Open Studies | United States

Gluten Free Diet in Preventing Graft Versus Host Disease in Patients Undergoing Donor Stem Cell Transplant

This study is not yet open for participant recruitment. (see Contacts and Locations)
Verified March 2017 by Rutgers, The State University of New Jersey
Sponsor:
Collaborator:
National Cancer Institute (NCI)
Information provided by (Responsible Party):
Rutgers, The State University of New Jersey
ClinicalTrials.gov Identifier:
NCT03102060
First received: March 30, 2017
Last updated: NA
Last verified: March 2017
History: No changes posted
  Purpose
This pilot clinical trial studies how well a gluten free diet works in preventing graft versus host disease in patients who are undergoing a donor stem cell transplant. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells (called graft versus host disease). A gluten free diet may decrease intestinal inflammation and graft versus host disease in patients who are undergoing a donor stem cell transplant.

Condition Intervention
Graft Versus Host Disease
Hematopoietic Cell Transplantation Recipient
Other: Dietary Intervention
Other: Laboratory Biomarker Analysis

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: No masking
Primary Purpose: Prevention
Official Title: Gluten Free Diet for GVHD Prophylaxis

Resource links provided by NLM:


Further study details as provided by Rutgers, The State University of New Jersey:

Primary Outcome Measures:
  • Rate and severity of stage 2-4 GI acute (a)GVHD as determined by microbiome analysis of stool samples [ Time Frame: Up to 12 months post allo-SCT ]
    To determine how often patients develop gastrointestinal graft-versus-host disease at various times after transplant

  • Rate and severity of all grade aGVHD and chronic GVHD as determined by microbiome analysis of stool samples [ Time Frame: Up to 12 months post allo-SCT ]
    To determine what the severity is if graft-versus host disease develops.

  • Rate of compliance with GFD [ Time Frame: Up to 30 days ]
    Adherence to diet will be recorded in a food diary. Compliance will be defined as > 67% of meals being gluten free.


Estimated Enrollment: 70
Anticipated Study Start Date: June 2017
Estimated Study Completion Date: March 2023
Estimated Primary Completion Date: March 2023 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Prevention (gluten free diet)
Patients undergo a gluten free diet for 30 days during initial hospitalization for allo-SCT, from the time of admission to discharge.
Other: Dietary Intervention
Undergo gluten free diet
Other Names:
  • Dietary Modification
  • intervention, dietary
  • Nutrition Intervention
  • Nutrition Interventions
  • Nutritional Interventions
Other: Laboratory Biomarker Analysis
Correlative studies

Detailed Description:

PRIMARY OBJECTIVES:

I. To determine the rate and severity of gastrointestinal (GI) graft versus host disease (GVHD) in patients assigned to, and compliant with, a gluten free diet (GFD) during initial transplant hospitalization.

SECONDARY OBJECTIVES:

I. To determine the tolerance of, and compliance with, a GFD in patients undergoing allogeneic hematopoietic stem cell transplant (allo-SCT).

OUTLINE:

Patients undergo a gluten free diet for 30 days during initial hospitalization for allo-SCT, from the time of admission to discharge.

After completion of study, patients are followed up at 1, 3, 6, and 12 months.

  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patient undergoing an allo-SCT
  • No history of celiac disease or non-celiac gluten sensitivity
  • Male and female and all ethnic groups are eligible

Exclusion Criteria:

  • Pregnant women
  • Children are not eligible as the transplant program is certified as an adult only transplant program
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT03102060

Locations
United States, New Jersey
Rutgers Cancer Institute of New Jersey Not yet recruiting
New Brunswick, New Jersey, United States, 08903
Contact: Roger K. Strair    732-235-7298    strairrk@cinj.rutgers.edu   
Principal Investigator: Roger K. Strair         
Sponsors and Collaborators
Rutgers, The State University of New Jersey
National Cancer Institute (NCI)
Investigators
Principal Investigator: Roger Strair Rutgers Cancer Institute of New Jersey
  More Information

Responsible Party: Rutgers, The State University of New Jersey
ClinicalTrials.gov Identifier: NCT03102060     History of Changes
Other Study ID Numbers: 021701
NCI-2017-00438 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
021701 ( Other Identifier: Rutgers Cancer Institute of New Jersey )
P30CA072720 ( US NIH Grant/Contract Award Number )
Study First Received: March 30, 2017
Last Updated: March 30, 2017

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Graft vs Host Disease
Immune System Diseases

ClinicalTrials.gov processed this record on April 24, 2017