Oligosaccharide for Cdiff(+) Heme-onc Patients

কেবল নিবন্ধিত ব্যবহারকারীরা নিবন্ধগুলি অনুবাদ করতে পারবেন

প্রবেশ করুন - নিবন্ধন করুন

লিঙ্কটি ক্লিপবোর্ডে সংরক্ষিত হয়েছে

স্থিতিনিয়োগের

স্পনসর

Medical College of Wisconsin

ক্লিনিকাল ট্রায়াল: NCT03778606

BioSeek: nct03778606

কীওয়ার্ডস

বিমূর্ত

Clostridium difficile causes ~453,000 infections and ~29,300 deaths per year in the US, making it the most common hospital acquired infection in the country. C. difficile is an anaerobic bacterium that has the capacity to inhabit the colon of humans and other mammals. Initially thought to be a commensal, it was later found to be associated with antibiotic induced enterocolitis. Since then, it has gradually become one of the most important healthcare associated pathogens. C. difficile infection (CDI) causes colitis, which is inflammation of the colonic mucosa with a spectrum of severity from mild to more protracted diarrhea, abdominal pain, fever, toxic megacolon, sepsis, and in some instances death. Mortality occurs despite the existence of three antibiotic options. CDI is also associated with higher hospital readmission rates, and associated healthcare costs in the US are estimated at 4.8 billion dollars annually. Due to the significance of C. difficile in healthcare, hospital level C. difficile rates are publically reported and closely scrutinized by the Centers for Medicare and Medicaid. Standard infection control bundles are proving to be insufficient for controlling the national C. difficile problem. Better understanding of the biological steps preceding clinical infection and reversal of the underlying gut dysbiosis will allow us to curtail our C. difficile epidemic. The present study aims to manipulate the gut microbiota to halt the biological progression of C. difficile.

CDI is a serious problem in hematology-oncology patients. The incidence of CDI in the hematology-oncology population is much higher than in other populations and hematology-oncology inpatient units frequently have the highest incidence of CDI cases within an institution. Additionally, hematology-oncology patients have high rates of C. difficile colonization upon hospitalization and more than 50% of patients detected with C. difficile colonization before bone marrow transplantation end up diagnosed with hospital associated CDI. This finding is not trivial as CDI treatment with oral vancomycin causes major and prolonged perturbations of their intestinal microbiota, which has been associated with higher mortality. In addition to the usual complications of CDI, a higher incidence of graft-versus-host-disease has been described in patients with CDI.

বর্ণনা

Aim 1/Objective 1. Establish the feasibility of oligosaccharide supplementation and twice a week stool collections among 12 C. difficile colonized hematology-oncology inpatients. It will be determined if at least 70% of the oligosaccharide dosages are taken by at least 8 (>=66%) of the 12 enrolled patients. Additionally, the ability to collect at least 50% of the scheduled stool samples will be evaluated.

Aim 1 will provide important information about the ideal food/drink to mix the potato starch supplemented in this study. The knowledge gained in this pilot will be used to design a future phase II or III clinical trial.

Aim 2. Explore the impact of oligosaccharide supplementation on C. difficile loads and relative abundance of Firmicutes. All stool samples will undergo 16S ribosomal ribonucleic acid (rRNA) and bioinformatics at the MCW's Genomic and Precision Medicine Center and C. difficile quantitative polymerase chain reaction (qPCR) at the PI's research laboratory. Historical controls will be obtained from a group of over 450 hematology-oncology inpatients who underwent at least one C. difficile surveillance test and whose stool samples are currently being processed for 16S rRNA by the PI's team. Controls at a 3:1 ratio with cases will be matched based on underlying disease, unit of admission, antibiotic use, baseline C. difficile fecal loads, and baseline relative abundance of Firmicutes.

Objective 2a. Evaluate the impact of oligosaccharide supplementation on the change of C. difficile fecal loads when compared to historical controls.

Objective 2b. Explore the effect of oligosaccharide supplementation on the change in relative abundance of Firmicutes when compared to historical controls.

It is expected a reduction will occur in C. difficile fecal loads during oligosaccharide supplementation when compared to matched controls. Conversely, it is expected an increase in the relative abundance of Firmicutes (or some of its operational taxonomic units; OTUs) during oligosaccharide replacement will occur when compared to matched controls. The knowledge gained with Objectives 2a and 2b will be used to determine the sample size needed to design future phase II or phase III clinical trials.

তারিখ

সর্বশেষ যাচাই করা হয়েছে:	11/30/2019
প্রথম জমা দেওয়া:	11/29/2018
আনুমানিক তালিকাভুক্তি জমা দেওয়া হয়েছে:	12/13/2018
প্রথম পোস্ট:	12/18/2018
সর্বশেষ আপডেট জমা দেওয়া হয়েছে:	12/08/2019
সর্বশেষ আপডেট পোস্ট:	12/10/2019
আসল অধ্যয়ন শুরুর তারিখ:	05/31/2019
আনুমানিক প্রাথমিক সমাপ্তির তারিখ:	05/31/2020
আনুমানিক অধ্যয়ন সমাপ্তির তারিখ:	06/30/2020

অবস্থা বা রোগ

Clostridium Difficile

Hematologic Diseases

হস্তক্ষেপ / চিকিত্সা

Dietary Supplement: Potato starch supplementation

পর্যায়

বাহু গ্রুপ

বাহু	হস্তক্ষেপ / চিকিত্সা
Experimental: Potato starch supplementation Twelve patients found to be colonized with C. difficile will undergo twice a day potato starch supplementation.	Dietary Supplement: Potato starch supplementation Potato starch will be given twice a day for up to 14 days, discharge, or death, whichever occurs first.

যোগ্যতার মানদণ্ড

বয়স অধ্যয়নের জন্য যোগ্য	18 Years প্রতি 18 Years
লিঙ্গ অধ্যয়নের জন্য যোগ্য	All
স্বাস্থ্যকর স্বেচ্ছাসেবীদের গ্রহণ করে	হ্যাঁ
নির্ণায়ক	Inclusion Criteria: Patients must meet all inclusion criteria to be eligible to participate in the study. - Patients must be at least 18 years of age at time of consent. - Positive C. difficile surveillance test. - Absence of diarrhea or abdominal pain within the past 48 hours. - Patient admitted in a hematology-oncology unit which for the purposes of this study will be defined as 7-CFAC and 8-CFAC. Exclusion Criteria: Patients must NOT meet any exclusion criteria to be eligible to participate in the study. - Presence of >= grade I nausea/vomiting. - Inability to take oral medications or food. - Expected length of hospitalization or survival less than 5 days - Patient is only boarding in hematology-oncology units and would have not otherwise been admitted to these units. - Unwillingness or inability to provide written informed consent. - Women known to be pregnant or lactating during the study. - History of inflammatory bowel disease.

ফলাফল

প্রাথমিক ফলাফল ব্যবস্থা

1. Stool samples will be collected twice a week while on potato starch supplementation and 1 time at 7-days post- starch supplementation to assess any changes in the frequency of collection during the 21-day period. [Day 1- Day 21]

Samples will be collected twice a week (4-5 times during supplementation) and one time at day 21 or discharge, whichever happens first.

2. Oligosaccharide intake assessed by a patient diary to measure supplementation feasibility [Day 1-Day 14]

Patients will be provided with a diary in which they will document compliance with oligosaccharide intake. It is anticipated ≥70% of intended doses to be fully administered by the patient.

3. The feasibility of collecting all available stool samples stool will be assessed. A rate ≥50% of correctly collected and processed samples will be considered feasible. [Day 1-Day 14]

It is expected ≥50% of stool samples to be correctly collected and processed.

মাধ্যমিক ফলাফলের ব্যবস্থা

1. Changes in C. difficile loads will be assessed using C. difficile quantitative polymerase chain reaction (qPCR). [Day 1-Day 14]

Stool samples collected for diagnosis and any additional stool collections will be thawed in batches and one cc aliquot will be extracted refreezing the remaining sample at -80 degrees F. One cc aliquot will then be divided into 4 sub-samples of equal volume and with the same unique identifier. This identifier will be able to chronologically cluster samples by each unique patient. A sample will be used for C. difficile qPCR quantitative determination.

2. Changes in Firmicutes' relative abundance due to oligosaccharide supplementation measured by 16S rRNA gene sequencing [Day 1-Day 14]

Sub-sample of stool from diagnosis, and additional stool collections will be used for 16S ribosomal ribonucleic acid gene sequencing to determine the microbiome community structure

Oligosaccharide for Cdiff(+) Heme-onc Patients

কীওয়ার্ডস

আলু

ribonucleic acid

oligosaccharide

স্টার্চ

সেপসিস

abdominal pain

উদরাময়

প্রদাহ

জ্বর

dysbiosis

colitis

enterocolitis

megacolon

অ্যান্টিবায়োটিক