Comparison of Two Surgical Treatments for Necrotizing Enterocolitis in Human Infants
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|ClinicalTrials.gov Identifier: NCT00252681|
Recruitment Status : Completed
First Posted : November 11, 2005
Last Update Posted : July 21, 2006
|Condition or disease||Intervention/treatment||Phase|
|Necrotizing Enterocolitis||Procedure: laparotomy Procedure: primary peritoneal drainage||Not Applicable|
This is a multi-center randomized clinical trial comparing laparotomy vs peritoneal drainage for perforated Necrotizing Enterocolitis. The current literature does not allow an objective comparison between these two methods. A recent comprehensive meta-analysis of all published and much unpublished data regarding the use of these procedures in the treatment of perforated NEC revealed that the degree of bias in assignment to treatment precluded an adequate determination as to the best treatment. The conclusion that only a randomized clinical trial would answer this question has led to this multi-center effort. The relative infrequency of the disease at any one neonatal center has necessitated enrollment of patients at many centers.
Comparison: Premature neonates weighing less than 1500 grams at birth who develop perforated necrotizing enterocolitis are randomized within two birth weight blocks (<1000 gms and 1000 - 1499 gms) for treatment with either laparotomy or primary peritoneal drainage. Daily postoperative clinical care is kept uniform between the two groups by means of a critical care pathway. The primary outcome variable is mortality, i.e. death within 90 days of intervention. The main secondary outcome is short bowel syndrome - defined as the need for chronic parenteral nutrition greater than 3 months following operation.
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||130 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Surgery for Necrotizing Enterocolitis in Human Infants: A Randomized Trial|
|Study Start Date :||July 1999|
|Study Completion Date :||June 2005|
- The primary outcome variable is operative mortality, i.e. death within 90 days of intervention.
- The secondary outcome is short bowel syndrome - defined as the need for chronic parenteral nutrition greater than 3 months following operation.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00252681
|United States, Connecticut|
|Yale University School of Medicine Section of Pediatric Surgery|
|New Haven, Connecticut, United States, 06520|
|Principal Investigator:||R. Lawrence Moss, MD||Yale University|