A double blinded randomized trial to see if the use of modified ultrafiltration during surgery effects post-operative recovery course in patients undergoing surgery for congenital heart defects.
Not Applicable
- Conditions
- Health Condition 1: Q243- Pulmonary infundibular stenosis
- Registration Number
- CTRI/2017/11/010512
- Lead Sponsor
- All India Institute of Medical Sciences New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with undergoing cardiac surgery for congenital cardiac defects with weight less than 20 kgs
2.Patients with cardiopulmonary bypass time more than 45 minutes
Exclusion Criteria
1.Patients with other non-cardiac comorbidities which might influence or confound the outcome variables
a.Coagulopathies
b.Children with respiratory compromise pre-operatively
c.Haemolytic anaemia
d.Sepsis
e.Previous sternotomy (redo procedures)
f.Patients undergoing emergency/palliative procedures (shunt procedures)
2.Parents/guardians not willing to give consent to participate in this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method