Rate of Bronchopulmonary Dysplasia in Preterms Neonates: a Trial Comparing SMOFlipid and Medialipide
NCT02853253 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL
Last updated 2019-07-24
Summary
SMOF is a large double blind placebo-controlled randomized clinical trial aiming to compare the rate of bronchopulmonary dysplasia (BPD) at 36 weeks corrected age in premature infants \< 29 weeks and / or with birth weight \< 1000 g receiving either SMOFlipid® or Medialipide® 20%. This study will offer new information for optimizing the management of preterms requiring parenteral nutrition. The investigators hypothesis is that the composition of SMOFlipid may decrease lipid peroxidation and oxidative stress in preterms, resulting in a lower incidence of BPD.
Conditions
- Preterm Neonates
Interventions
- DIETARY_SUPPLEMENT
-
SMOFlipid®
SMOFlipid® (FreseniusKabi France, Sèvres, France). It is a 3rd generation LE containing a physical mixture of soybean oil (30%), MCT (30%), olive oil (25%) and fish oil (15%). Its ratio omega6/omega 3 is 2,5/1. SMOF will be initiated within the 1st day of life of neonates and will be prescribed daily by the attending physician following these guidelines: initiation rate: 1 g/kg/day; daily increase: 0.5 to 1 g/kg/day ; target: 3 to 4 g/kg/day. All included preterms will receive nutritional support according to a single protocol based on the ESPGHAN recommendations: parenteral glucose and amino acids (Primene 10%, Clintec Parenteral, Maurepas, France) soon after birth (in their 1st day of life). Initiation rate of parenteral glucose and amino acids will be 6 to 8 g/kg/day and 2 g/kg/day respectively. The daily increase of parenteral glucose and amino acids will be 1 to 2 g/kg/day and 0.5 g/kg/day respectively, for a target rate of 14 to 17 g/kg/day and 3.5 g/kg/day respectively.
- DIETARY_SUPPLEMENT
-
Medialipide®
Medialipide® 20% (B Braun Medical, Boulogne, France). It is a second generation LE containing soybean oil (50%) and MCT (50%). Its ratio omega6/omega 3 is 7/4. Medialipide will be initiated within the 1st day of life of neonates and will be prescribed daily by the attending physician following these guidelines: initiation rate: 1 g/kg/day ; daily increase: 0.5 to 1 g/kg/day; target: 3 to 4 g/kg/day. All included preterms will receive nutritional support according to a single protocol based on the ESPGHAN recommendations: parenteral glucose and amino acids (Primene 10%, Clintec Parenteral, Maurepas, France) soon after birth (in their 1st day of life). Initiation rate of parenteral glucose and amino acids will be 6 to 8 g/kg/day and 2 g/kg/day respectively. The daily increase of parenteral glucose and amino acids will be 1 to 2 g/kg/day and 0.5 g/kg/day respectively, for a target rate of 14 to 17 g/kg/day and 3.5 g/kg/day respectively.
Sponsors & Collaborators
-
Hospices Civils de Lyon
lead OTHER
Principal Investigators
-
Olivier CLARIS, Pr · Hospices Civils de Lyon
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 6 Hours
- Max Age
- 1 Day
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-01-31
- Primary Completion
- 2019-05-31
- Completion
- 2019-05-31
Countries
- France
Study Locations
More Related Trials
-
Outcome of Extremely Preterm Infants Who Received Systemic Postnatal Corticosteroid for Bronchopulmonary Dysplasia
NCT05055193 ·Status: COMPLETED
-
Risk Factors in Bronchopulmonary Dysplasia (Newborn Lung Project)
NCT00005289 ·Status: COMPLETED
-
Antecedents of Bronchopulmonary Dysplasia
NCT00005293 ·Status: COMPLETED
-
Gastrointestinal Microbiome Influence on the Development of Bronchopulmonary Dysplasia
NCT03229967 ·Status: COMPLETED
-
Physiologic Definition of Bronchopulmonary Dysplasia
NCT01223287 ·Status: COMPLETED
-
Biomarkers and Volumetric Capnography in BPD
NCT02083562 ·Status: COMPLETED
-
Efficacy and Safety Evaluation of Pneumostem® Versus a Control Group for Treatment of BPD in Premature Infants
NCT01828957 ·Status: COMPLETED ·Phase: PHASE2
-
Duodenal Feeds in Very Low Birth Weight Infants
NCT04246333 ·Status: COMPLETED ·Phase: NA
-
Study of the Pathobiology of Bronchopulmonary Dysplasia in Newborns
NCT00006058 ·Status: COMPLETED
-
The Treatment of Bronchopulmonary Dysplasia by Instillation PS and Mononuclaer Cells in Preterms
NCT03855202 ·Status: UNKNOWN ·Phase: PHASE1
-
Stem Cells for Bronchopulmonary Dysplasia
NCT03378063 ·Status: WITHDRAWN ·Phase: EARLY_PHASE1
-
Genetic Susceptibility for Bronchopulmonary Dysplasia in Preterm Infants
NCT00904774 ·Status: UNKNOWN
-
The Baby Lung Study
NCT05152316 ·Status: COMPLETED
-
Dexamethasone Regimens for BPD Prevention in Preterm Infants
NCT07052201 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Use of Mesenchymal Stem Cells in Pre-term Patients With Bronchopulmonary Dysplasia.
NCT06270199 ·Status: RECRUITING ·Phase: PHASE2
-
Body Weight Growth After Birth and Bronchopulmonary Dysplasia
NCT05053269 ·Status: WITHDRAWN
-
Benchmarking Initiative to Reduce Bronchopulmonary Dysplasia
NCT00067613 ·Status: COMPLETED ·Phase: NA
-
Ultrasound Assessment of Diaphragmatic Function in Infants With BPD
NCT04941963 ·Status: COMPLETED
-
The Effects of Two Different Intravenous Lipid Emulsions on the Outcomes of Preterm Infants With Sepsis
NCT03275090 ·Status: COMPLETED ·Phase: PHASE4
-
Intratracheal Umbilical Cord-derived Mesenchymal Stem Cell for the Treatment of Bronchopulmonary Dysplasia (BPD)
NCT03645525 ·Status: WITHDRAWN ·Phase: PHASE1/PHASE2
-
Safety of Furosemide in Premature Infants at Risk of Bronchopulmonary Dysplasia (BPD)
NCT02527798 ·Status: COMPLETED ·Phase: PHASE2
-
Restricted Versus Liberal Fluid Intake for Prevention of Bronchopulmonary Dysplasia
NCT06954142 ·Status: RECRUITING ·Phase: NA
-
Follow-up Safety and Efficacy Evaluation on Subjects Who Completed PNEUMOSTEM® Phase-II Clinical Trial
NCT01897987 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy of Umbilical Cord-derived Mesenchymal Stem Cell(MSC) Transplantation in the Treatment of Bronchopulmonary Dysplasia(BPD) in Premature Infants
NCT06788470 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Safety and Efficacy of MSC-EVs in the Prevention of BPD in Extremely Preterm Infants
NCT06279741 ·Status: RECRUITING ·Phase: PHASE1/PHASE2