Comparison of Conventional fluid Resuscitation and Bolus fluid Resuscitation in preoperative optimization of patients with Infantile Hypertrophic Pyloric stenosis

Completed

• Conditions: Infantile Hypertrophic Pyloric StenosisPreoperative optimization; Infantile Hypertrophic Pyloric Stenosis; Preoperative optimization; Bolus therapy; Optimization

• Registration Number: TCTR20190512002
• Lead Sponsor: none

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-05-12
• Study Completion: 2022-02-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1. Infants admitted in the pediatric surgery department with a diagnosis of infantile hypertrophic pyloric stenosis
2. The parents/legal guardian gives consent for inclusion in the study

Exclusion Criteria

1. Patient in renal failure
2. Patient in sepsis
3. Withdraws consent for inclusion in the study
4. A different diagnosis at surgery
5. Plan of surgery changed pre-operatively or intra-operatively
6. Other co-morbidity

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to preoperative optimization After start of either conventional or bolus fluid therapy hours

Secondary Outcome Measures

Name	Time	Method
Hospital Stay at the time of discharge hours