- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05623098
Effects of Dietary Fiber on Bone Metabolism
Effects of Dietary Fiber Enteral Nutrition on Bone Metabolism in Septic Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In recent years, researchers have found that the incidence of bone loss in ICU patients is significantly higher than that in the control group of the same age, patients with sepsis whose bone balance is disrupted by higher overresorption, bone destruction and release of multiple active cytokines and toxins become the"Invisible killer"of the ICU, however, the pathogenesis of osteoporosis is not clear, and the existing drugs for osteoporosis can not be safely used in critically ill patients. The gastrointestinal tract is the"Initiating organ"and"Central organ" of multiple organ dysfunction and forms a complex and powerful"Gut-bone axis"with bone, which plays a key role in bone metabolism, but the mechanism is unclear. The human gut contains a dense and diverse microbial community, which plays an important role in nutrition, metabolism and immunity, small intestinal microecology can affect bone turnover through a variety of pathways, especially the metabolite short-chain fatty acid FAS (SCFAs) , which can inhibit osteoclast activity by regulating inflammatory cytokines and immune cells, promote the formation of osteoblasts and other aspects to maintain the stability of bone metabolism, and then protect the health of bones, forming a"Gut-microcology-bone"axis.
Clinical and animal studies have found that sepsis can lead to a serious imbalance in the gut microecology, a reduction in probiotics, a reduction in short-chain fatty acid, a reduction in bone mass, and an increase in bone destruction, maintaining the stability of microecology can be one of the effective means of bone protection. But at present, the treatment of sepsis with early supplementation of probiotics is still controversial, and dietary fiber intake has significantly changed the composition of the microbiota, it may be a safe and effective method to prevent bone loss in sepsis. Further study on it will provide reliable theoretical basis and intervention target for early, safe and effective prevention of osteoporosis. Therefore, based on the above research background, Investigators intend to evaluate the overall safety and efficacy of dietary fiber-containing enteral nutrition supplementation in patients with sepsis by observing changes in bone metabolism-related indicators, to provide the basis for further basic and mechanism research
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Guangdong
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Guangzhou, Guangdong, China, 510515
- Zhujiang Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- The subjects voluntarily cooperated with the study and signed the informed consent form, and could be followed up
- Age 18-70
- It meets the diagnostic criteria of Sepsis 2016 Sepsis 3.0 guidelines
- After treatment, the Hemodynamics is stable and the patient is ready to start enteral nutrition support
- Those who need tube feeding for more than 14 days because of the need of illness and can not take food by mouth
Exclusion Criteria:
- People who have had osteoporosis in the past
- Admission due to fracture
- The shock was not corrected, and the patients were maintained with a large amount of vaso-active drugs (0.5 ug/kg/min of noradrenaline) , but could not be given enteral nutrition
- Supplement with probiotics or prebiotics alone
- Parturients
- No written informed consent
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Dietary fiber was not added to enteral nutrition preparation
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Dietary fiber was added to enteral nutrition preparation
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Whether to add nutrients containing dietary fiber
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The changes of bone metabolic markers β-CTX
Time Frame: 28 day
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The venous blood was drawn daily before and after the enrollment (the first, third, seventh and fourteenth days) ,and β- CTX for comparison
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28 day
|
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The changes of bone metabolic markers PINP
Time Frame: 28 day
|
28 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in intestinal flora
Time Frame: 28 day
|
Collect stool before and after the enrollment (the first, third, seventh and fourteenth days) ,observe the changes of intestinal flora in the two groups.
Total bacterial DNA were extracted from samples using the QIAamp DNA stool Mini Kit from Qiagen according to the manufacture's protocol.
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28 day
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Changes in short-chain fatty acid of metabolites
Time Frame: 28 day
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Collect stool before and after the enrollment (the first, third, seventh and fourteenth days) ,observe the changes of metabolite short chain fatty acids in the two groups.
Fresh feces were collected and frozen in liquid nitrogen timely.SCFAs was extracted and quantified using a Metrohm ion chromatograph(850 Professional Ic, Metrohm, Herisau, Switzerlan) system
|
28 day
|
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Abdominal symptoms (abdominal distention)
Time Frame: 28 day
|
To evaluate and compare the difference of abdominal symptoms (abdominal distension) between the two groups,It is divided into three levels according to the severity of abdominal distension, it can be divided into light, medium and severe (for example:Mild, soft abdomen, tolerable,Moderate: abdominal bulge, obvious discomfort,Severe: abdominal muscles are obviously tense/intolerable)
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28 day
|
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Abdominal symptoms ( diarrhea incidence)
Time Frame: 28 day
|
To evaluate and compare the difference of abdominal symptoms (diarrhea incidence ) between the two groups,it can be divided into light, medium and severe (for example:Mild, 3-5 times/day, 250-500ml/day,Moderate:>5 times/day, 500-1000ml/day,Severity:>5 times/day,>1500ml/day)
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28 day
|
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The change of systemic inflammatory response index: the value of TNF-α in systemic inflammatory response
Time Frame: 28 day
|
The changes of TNF-α were observed and compare before and after treatment, It can be tested in the laboratory of our hospital, the higher the value, the heavier the infection.
|
28 day
|
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The change of systemic inflammatory response index: the value of IL-6 in systemic inflammatory response
Time Frame: 28 day
|
The changes of IL-6 were observed and compare before and after treatment.
It can be tested in the laboratory of our hospital, the higher the value, the heavier the infection
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28 day
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The change of systemic inflammatory response index: the value of Procalcitonin in systemic inflammatory response
Time Frame: 28 day
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The changes of procalcitonin were observed and compare before and after treatment, the higher the value, the heavier the infection
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28 day
|
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Length of ICU stay
Time Frame: 28 day
|
The total hospitalization time were observed before and after treatment
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28 day
|
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Length of Apache II score
Time Frame: 28 day
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The total Apache II score were observed before and after treatment,The higher the score is, the more serious the disease is.
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28 day
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022LX0036_GC
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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