Effects of Recto-colic Enemas of Butyrate on the Digestive Disorders of Very Low Birth Weight Preterms <1250 Grams (NEOTRANS)
Primary Purpose
Very Low Birth Weight Preterms
Status
Terminated
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Butyrate enemas
Sponsored by
About this trial
This is an interventional treatment trial for Very Low Birth Weight Preterms focused on measuring Butyrate, Preterms, Very Low Birth Weight (<1250g), Rectocolonic enemas, Digestive maturation, Parenteral nutrition weaning, ECUN, Whole gut transit time
Eligibility Criteria
Inclusion Criteria:
- Any preterm infant with a birth weight less than or equal to 1250 grams admitted in the neonatal intensive care unit of Nantes Hospital
- Inborn or outborn
- No signs of gastrointestinal perforation or ECUN
- Absence of severe congenital disease
- Written informed consent of parental authority.
Exclusion Criteria:
- Newborn with birth weight greater than 1250 grams,
- Gestational age > 30 AG
- Digestive pathology diagnosed prior PND5: perforation, necrotizing enterocolitis, malformations
- Severe congenital pathology inconsistent with clinical assessment.
- Parental Refusal
Sites / Locations
- Nantes
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Butyrate
Therapeutic Abstention
Arm Description
New born with a birth weight <1000g: Seven enemas of butyrate will be performed every 2 days from PND5 New born with a birth weight >1000g: Seven enemas of butyrate will be performed every day from PND5
The protocol will pretend enema: instillation in the diaper the product under consideration, to make the two indistinguishable processes (time, odor, wicking diaper ...)
Outcomes
Primary Outcome Measures
Efficacy of colonic butyrate enemas in digestive maturation of preterms
The primary outcome of NEOTRANS study consists in the evaluation of the effects of colonic butyrate enemas upon the digestive maturation of preterms.
This endpoint is based on a clinical criteria that is the delay of weaning of the parenteral nutrition support. An increase of 25% (50 vs 75%) will be considered clinically significant.
Parenteral nutrition weaning is defined as the day where enteral caloric intake reach 80% of total calories.
Secondary Outcome Measures
Gastrointestinal complications frequency
Nosocomial infections frequency
Iatrogenic effect
whole gut transit time (red carmine test)
Growth
Comparaison between 2 arms of height, weight and head circumference
Invasive ventilation support
Bronchopulmonary dysplasia incidence
Hospitalization duration
Neuromotor development
ASQ questionnaire
Full Information
NCT ID
NCT01536483
First Posted
February 16, 2012
Last Updated
May 10, 2016
Sponsor
Nantes University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01536483
Brief Title
Effects of Recto-colic Enemas of Butyrate on the Digestive Disorders of Very Low Birth Weight Preterms <1250 Grams
Acronym
NEOTRANS
Official Title
Effects of Recto-colic Enemas of Butyrate on the Digestive Disorders of Very Low Birth Weight Preterms <1250 Grams. Clinical Trial Prospective, Monocentric, Randomized in Double-blinded.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Terminated
Why Stopped
The second intermediary analysis showed no significant difference between both arms
Study Start Date
February 2012 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nantes University Hospital
4. Oversight
5. Study Description
Brief Summary
Clinical management of very low birth weight newborns (VLBW <1250g) consists in several challenges to adapt immature physiological systems to extrauterine life. Advances in neonatal medicine for pulmonary and/or neurological and/or cardiovascular diseases have significantly improved outcomes of these children. However, the gastro-intestinal (GI) tract remains a major cause of morbidity due to
the immaturity of GI functions (prolonged ileus, bacterial overgrowth and translocation),
the complication of GI tract immaturity: intestinal perforation and enterocolitis necrotizing)
the need of a prolonged parenteral nutrition and its complications (central venous catheter infections, sepsis, electrolyte disturbances) but without generate a high proof level on this targeted population (<1250g).
The GI functions are progressively acquired during development and are largely sensitive to the environment, especially the intestinal luminal content. Indeed, probiotics and prebiotics have shown beneficial effects upon GI functions of newborns. One of the metabolite of the gut flora potentially involved is the butyrate. Butyrate is a short chain fatty acid produced in the colon by the microbiota (carbo-hydrates degradation). The colonic amount of butyrate increases gradually after birth. The beneficial effects of butyrate are related to its properties upon the epithelial barrier (anti-inflammatory, antioxidant, barrier repair) and upon the enteric nervous system (network of neurons and glial cells) that regulate GI functions and in particular colonic motility.
To date, there is no clinical consensus to manage digestive disorders of VLBW. Several clinical studies have assessed the effects of prokinetic drugs, dietary supplements (probiotics, prebiotics) but without generate a high proof level on this targeted population. In this context, a recent study of our Research Unit (INSERM-CIC Mère-Enfant 004) has shown benefit effects of oral probiotics supplementation in children with birth weight greater than 1000g but not in extreme preterms with birth weight less than 1000g.
The main hypothesis to explain theses results lies in the intensive use of antibiotic and feeding interruption frequency in this targeted population which induce disturbances in the composition of the gut lumen (in particular the flora).
Colonic enemas assessed in various observational studies concerning VLBW seem to demonstrate a clinical efficiency upon the colonic transit, underlying by mechanical and osmotic mechanisms.
Here, the investigators propose to evaluate the clinical efficiency of butyrate enemas by a prospective randomized clinical trial blinded design.
The purpose of NEOTRANS study is to demonstrate that butyrate enemas may improve the nutritional management of extreme preterm less than 1250 grams, by facilitating the development of colic motility and clinical nutrition tolerance.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Very Low Birth Weight Preterms
Keywords
Butyrate, Preterms, Very Low Birth Weight (<1250g), Rectocolonic enemas, Digestive maturation, Parenteral nutrition weaning, ECUN, Whole gut transit time
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
61 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Butyrate
Arm Type
Experimental
Arm Description
New born with a birth weight <1000g: Seven enemas of butyrate will be performed every 2 days from PND5
New born with a birth weight >1000g: Seven enemas of butyrate will be performed every day from PND5
Arm Title
Therapeutic Abstention
Arm Type
No Intervention
Arm Description
The protocol will pretend enema: instillation in the diaper the product under consideration, to make the two indistinguishable processes (time, odor, wicking diaper ...)
Intervention Type
Drug
Intervention Name(s)
Butyrate enemas
Intervention Description
Seven enemas
Possibility to delay from 24 to 48 hours the procedure in case of clinical poor tolerance(maximum two enemas postponed and delayed at PND12 and PND13)
The study remains blinded for the investigation team through the intervention of a clinical research nurse
According to the procedure previously described by Nakaoka et al. (2009), a lubricated Foley catheter Ch 6 will be introduced into the rectum, the balloon will be inflated with 1 ml water for injections. Butyrate solution will be placed in a bag placed 50 cm above the child. Therefore, treatment administration will be performed at a controlled pressure of 50 cm H2O without any manual intervention
Installation time and retention is setted at 15 minutes
Treatment units will be directly placed in the incubator 30 min before the procedure to warm the enema to +36°C
Per-treatment clinical monitoring of the tolerance will be performed by a neonatologist
Primary Outcome Measure Information:
Title
Efficacy of colonic butyrate enemas in digestive maturation of preterms
Description
The primary outcome of NEOTRANS study consists in the evaluation of the effects of colonic butyrate enemas upon the digestive maturation of preterms.
This endpoint is based on a clinical criteria that is the delay of weaning of the parenteral nutrition support. An increase of 25% (50 vs 75%) will be considered clinically significant.
Parenteral nutrition weaning is defined as the day where enteral caloric intake reach 80% of total calories.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Secondary Outcome Measure Information:
Title
Gastrointestinal complications frequency
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Nosocomial infections frequency
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Iatrogenic effect
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
whole gut transit time (red carmine test)
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Growth
Description
Comparaison between 2 arms of height, weight and head circumference
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Invasive ventilation support
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Bronchopulmonary dysplasia incidence
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Hospitalization duration
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 5 weeks
Title
Neuromotor development
Description
ASQ questionnaire
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Days
Maximum Age & Unit of Time
5 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Any preterm infant with a birth weight less than or equal to 1250 grams admitted in the neonatal intensive care unit of Nantes Hospital
Inborn or outborn
No signs of gastrointestinal perforation or ECUN
Absence of severe congenital disease
Written informed consent of parental authority.
Exclusion Criteria:
Newborn with birth weight greater than 1250 grams,
Gestational age > 30 AG
Digestive pathology diagnosed prior PND5: perforation, necrotizing enterocolitis, malformations
Severe congenital pathology inconsistent with clinical assessment.
Parental Refusal
Facility Information:
Facility Name
Nantes
City
Nantes
Country
France
12. IPD Sharing Statement
Learn more about this trial
Effects of Recto-colic Enemas of Butyrate on the Digestive Disorders of Very Low Birth Weight Preterms <1250 Grams
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