Enteral Nutrition Tolerance and the Gut Microbiome Study

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Mayo Clinic

Status

Enrolling

Conditions

Enteral Feeding Intolerance

Treatments

Dietary Supplement: Polymeric Tube Feeds
Dietary Supplement: Blenderized Tube Feeds

Study type

Interventional

Funder types

Other

Identifiers

NCT03795870
18-004416

Details and patient eligibility

About

The current study will enroll patients who are going to require enteral nutrition support for at least 4 weeks and randomize them to standard polymeric formulas or blenderized tube feeding. They will be asked to fill out a questionnaire about their tolerance of enteral feeds. They will also be asked to provide stool samples before enrollment and after 4-6 weeks. The study is trying to assess whether the use of whole food in blenderized tube feeding will be better tolerated and also lead to greater diversity of microbiome.

Full description

Malnutrition remains highly prevalent in both acute and chronic diseases, leading to longer hospital length of stay, greater risk of hospital readmission, and overall increase in morbidity and mortality. Over the last few decades, studies have continued to reveal significant clinical benefit from nutrition support, including reduction in complications and length of stay, maintenance of gastrointestinal integrity, and overall improvement in clinical outcomes and mortality. Despite high prevalence of Home Enteral Nutrition(HEN), patients continue to struggle with intolerance of tube feeds leading to chronic underfeeding and weight loss. Current guidelines recommend using standard polymeric formula or high-protein standard formula in the hospitalized patient requiring EN and also recommend against routine use of formulas designed to be immune-modulatory, elemental/semi-elemental, disease-specific (diabetes), and organ-specific (hepatic, renal, pulmonary). Blenderized Tube Feeding(BTF) offers a number of advantages to standard polymeric formula including being able to modify the macro-nutrient and fiber content based on patient preference. BTF use has also been increasing significantly in the past few years. The gut microbiome, or gut host environment, consists of approximately 10 thousand cells and has been the subject of much interest as it relates to gastrointestinal homeostasis. Our aim therefore is to (1) characterize the structure and dynamics of complex microbial communities using 16S rRNA- encoding gene sequences; (2) determine how they change with EN and; (3) how they may be correlated with tolerance of EN. A total of fifty subjects who are willing to participate in current trial and who meet eligibility will be recruited from the Mayo Clinic HEN program. Suitable subjects will be identified when they present at the initial HEN visit prior to undergoing enteral tube placement. Written informed consent will be obtained from all individuals who participate in the study. The principal investigator or member of study team meet with each participant, review the consent form in detail and confirm the subject's understanding of the study. The study team will answer all questions posed by the participants and when convinced that the subject verbally demonstrates understanding of the protocol, they will obtain a signed consent. Only designated staff members are authorized to obtain informed consent. At the pre-enteral tube visit, subjects will complete a gastrointestinal quality of life (QoL) questionnaire which will form the baseline assessment for symptoms and functional status. Body composition will be measured using Bio-impedance analysis (BIA; InBody™). A stool specimen will be obtained for analysis of the gut microbiome at baseline. Baseline clinical data such as current medical problems will be recorded.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. All subjects who are above 18 years of age, who present to Mayo Clinic HEN program for initial evaluation prior to enteral tube placement
  2. Require enteral nutrition support for at least 4-6 weeks from enrollment

Exclusion criteria

  1. Patients with type 1 or 2 diabetes will be excluded due to the known pre-existing changes in the gut microbiome in this population.
  2. Patients who have had exposure to probiotics, prebiotics or antibiotics in the preceding 4 weeks will be excluded.
  3. Known allergy or intolerance to study products will be excluded.
  4. Patients on parenteral nutrition will be excluded.
  5. If oral feeding accounts for >25% of daily caloric intake.
  6. Presence of entero-cutaneous fistula
  7. Patients with short bowel syndrome will be excluded.
  8. Patients who have had bariatric surgery or other alteration of GI tract will be excluded.
  9. Hematologic malignancy with absolute neutrophil count < 500/mm3
  10. History of renal or liver transplant or on transplant list.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

Polymeric Tube Feeds
Active Comparator group
Description:
This arm will be receiving Polymeric Tube Feeds as a part of the regular HEN Protocol.
Treatment:
Dietary Supplement: Polymeric Tube Feeds
Blenderized Tube Feeds
Active Comparator group
Description:
This arm will be receiving Blenderized tube feeds as a part of the regular HEN Protocol.
Treatment:
Dietary Supplement: Blenderized Tube Feeds

Trial contacts and locations

1

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Central trial contact

Vishakantha (Vishu) Murthy, PhD; Manpreet S Mundi, MD

Data sourced from clinicaltrials.gov

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