Clinical Trials Logo
  1. Home
  2. Other
  3. NCT04083638
  4. Details
NCT04083638 Clinical Trial

The Relationship Between Erythrocyte Transfusion and Nutrition and Necrotizing Enterocolitis in Preterm Infants

Necrotizing Enterocolitis of Newborn Clinical Trial

Official title:
Investigation of the Relationship Between Erythrocyte Transfusion and Nutrition and Necrotizing Enterocolitis in Preterm Infants: a Randomized Controlled Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04083638
Other study ID # 2019/279
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2020

Study information
Verified date September 2019
Source Dr. Behcet Uz Children's Hospital
Contact Senem A Özdemir, MD
Phone 05327614670
Email drsenemalkan@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study; The aim of this study was to investigate the changes in fasting and dietary and mesenteric blood flow in the acute period during and after transfusion and to evaluate the necrotizing enterocolitis.

Recruitment information / eligibility
Status Recruiting
Enrollment 81
Est. completion date December 31, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group N/A to 1 Month
Eligibility Inclusion Criteria:

- <32 gestational week and/or <1500 g birth weight

Exclusion Criteria:

- Major congenital anomalies, hemodynamic instability

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• IFAB
Intestinal Fatty Acid Binding Protein will be taken from all participants before the tx and after the tx

Locations
Country Name City State
Turkey Behçet Uz Children's Hospital Izmirli Izmir

Sponsors (1)
Lead Sponsor Collaborator
Dr. Behcet Uz Children's Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary necrotizing enterocolitis 0-48 hours after tx
Primary Mortality If all babies die after tx study will be finished 0-24 hour after tx
See also
  Status Clinical Trial Phase
Completed NCT03926390 - Gut Priming With Oral Bovine Colostrum for Preterm Neonates; Randomized Control Trial N/A
Completed NCT03111329 - Does Routine Assessment of Gastric Residuals in Preterm Neonates Influence Time Taken to Reach Full Enteral Feeding? N/A
Recruiting NCT05619055 - The Intestinal Dysbacteriosis in the Pathogenesis of Necrotizing Enterocolitis
Recruiting NCT03549507 - CEUS Evaluation of Bowel Perfusion in Necrotizing Enterocolitis Phase 3
Completed NCT04977817 - Probiotics/TPN in the NICU
Completed NCT03136172 - Monitoring of Systemic or Organ Perfusion for Preterm Infants
Completed NCT04719546 - Risk Factors of Necrotizing Enterocolitis in Premature Newborns
Recruiting NCT03366584 - The Effect of β-Carotene, Vitamin D3 and Zinc on Hyaline Membrane Disease and Feeding Intolerance in Premature Neonates Phase 4
Not yet recruiting NCT05710575 - Role of Probiotic Use in Outcomes of Premature Birth N/A
Recruiting NCT05121753 - Infant Formula Feeding and Necrotizing Enterocolitis in Newborns
Recruiting NCT03997266 - NICU Antibiotics and Outcomes Trial Phase 4