Comparison of open and laparoscopic pyloromyotomy

Condition	Intervention
Pyloric Stenosis	Procedure: pyloromyotomy

Further Study Details: 

Primary Outcomes: Time to full feeds; Post operative length of stay; Episodes of post-operative vomiting
Secondary Outcomes: Peri-operative complications; Post-operative complications; Anaesthetic time; Operating time; Post-operative pain and analgesia requirements; Cosmetic outcome; Total in-hospital costs
Expected Total Enrollment:  200

Ages Eligible for Study:  up to  3 Months,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• All infants with pyloric stenosis

Exclusion Criteria:

-

Please refer to this study by ClinicalTrials.gov identifier  NCT00144924

Nigel Hall, Mr       n.hall@ich.ucl.ac.uk

United Kingdom
      Institute of Child Health/Great Ormond Street Hospital, London,  United Kingdom; Recruiting

Study chairs or principal investigators

Nigel Hall, Mr,  Principal Investigator,  Institute of Child Health   

Study ID Numbers:  03SG45
Last Updated:  September 2, 2005
Record first received:  September 2, 2005
ClinicalTrials.gov Identifier:  NCT00144924
Health Authority: United Kingdom: Research Ethics Committee
ClinicalTrials.gov processed this record on 2005-09-06