Necrotizing Enterocolitis Clinical Trial
— ProbioticsOfficial title:
Role of Probiotics for Prevention of Necrotizing Enterocolitis in Preterm Very Low Birth Weight Infants: A Double Blind Randomized Controlled Trial
Verified date | January 2016 |
Source | Sylhet M.A.G.Osmani Medical College |
Contact | n/a |
Is FDA regulated | No |
Health authority | Bangladesh: Ethical Review Committee |
Study type | Interventional |
This prospective randomized double-blind control trial is carrying out in the neonatal unit of Sylhet MAG Osmani Medical College Hospital, Sylhet between July 2012 to December 2015 with the diagnosis of preterm (<33 weeks gestation) VLBW (birth weight <1500g) and fulfilling the inclusion criteria (able to tolerate oral feed and survive beyond 48h of life) were included in this study. Babies with suspicion of clinical sepsis, presence of perinatal asphyxia, major congenital anomaly and babies who expired due to other neonatal illness were excluded. Gestation was assessed from history of last menstrual period and after birth by new Ballard scores. A study protocol was approved by the Institutional Ethics Committee of Sylhet M.A.G Osmani Medical College, Sylhet.
Status | Completed |
Enrollment | 60 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | N/A to 33 Weeks |
Eligibility |
Inclusion Criteria: - All newborn infant preterm (<33 weeks gestation to 28 weeks gestation) VLBW (birth weight <1500gm to 1000 gm) - Able to tolerate oral feed - Informed consent by the parents or guardian Exclusion Criteria: - Evidence or suspicion of clinical sepsis before the baby is randomised - Presence of perinatal asphyxia - Presence of major congenital anomali - Death within first week of life due to other neonatal illness |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Sylhet M.A.G.Osmani Medical College |
Deshpande G, Rao S, Patole S. Probiotics for prevention of necrotising enterocolitis in preterm neonates with very low birthweight: a systematic review of randomised controlled trials. Lancet. 2007 May 12;369(9573):1614-20. Review. — View Citation
Forchielli ML, Walker WA. The effect of protective nutrients on mucosal defense in the immature intestine. Acta Paediatr Suppl. 2005 Oct;94(449):74-83. — View Citation
Neish AS, Gewirtz AT, Zeng H, Young AN, Hobert ME, Karmali V, Rao AS, Madara JL. Prokaryotic regulation of epithelial responses by inhibition of IkappaB-alpha ubiquitination. Science. 2000 Sep 1;289(5484):1560-3. — View Citation
Sharma R, Tepas JJ 3rd, Hudak ML, Mollitt DL, Wludyka PS, Teng RJ, Premachandra BR. Neonatal gut barrier and multiple organ failure: role of endotoxin and proinflammatory cytokines in sepsis and necrotizing enterocolitis. J Pediatr Surg. 2007 Mar;42(3):454-61. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Necrotizing Enterocolitis: Occurrence of NEC (stage II and III) by Modified Bell's classification | The occurrence of NEC (stage II and III) by modified Bell's classification | 10 days | Yes |
Secondary | Enteral feeding | days to achieve full enteral feeding | 10 days | Yes |
Secondary | Hospital stay | maximum days of hospital stay | 10 days | Yes |
Secondary | weight in Kg | weight in kg | 10 days | Yes |
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