Clinical Trials Logo

Clinical Trial Summary

The overall objective of this research study is to determine the effect of a pre-operatively placed nasogastric tube compared to no nasogastric tube, on post-operative emesis rates and postoperative length of stay in infants with a primary diagnosis of pyloric stenosis treated with pyloromyotomy. This study will also examine the feasibility data of the pilot data to develop estimates of treatment effect of a pre-operative nasogastric tube on post-operative rate of emesis and length of stay to be used to determine the sample size of the definitive trial.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01139853
Study type Interventional
Source McMaster University
Contact
Status Completed
Phase Phase 0
Start date January 2010
Completion date January 2015

See also
  Status Clinical Trial Phase
Completed NCT00409734 - Frequency of Formula Change Prior to the Accurate Diagnosis of Pyloric Stenosis
Terminated NCT02775214 - Conventional Direct Laryngoscopy Vs. Video Laryngoscopy With The C-MAC For Pyloromyotomy N/A
Completed NCT02359305 - Institutional Audit of the Use of Intravenous Acetaminophen in Infants Undergoing Pyloromyotomy N/A
Terminated NCT00144924 - Open vs Laparoscopic Pyloromyotomy for Pyloric Stenosis N/A
Completed NCT03650842 - Changes in Cerebral Oxygenation During Laparoscopic Pyloromyotomy N/A