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

Comparison of Conventional Fluid Resuscitation and Bolus Fluid Resuscitation in the Pre-Operative Optimization of Infantile Hypertrophic Pyloric Stenosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190512002
Enrollment
100
Registered
2019-05-12
Start date
2019-01-06
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infantile Hypertrophic Pyloric Stenosis Preoperative optimization Infantile Hypertrophic Pyloric Stenosis Preoperative optimization Bolus therapy Optimization

Interventions

Bolus fluid therapy will be administered as bolus of normal saline 20ml/kg over a span of 1 hour in addition to normal daily maintenance fluids. The number of boluses will be decided as under
Patients with abnormal Cl&#45
33 or >40 mEq/L will require 2&#44
3 boluses&#44
respectively. Patient with normal Cl&#45
and HCO3 but abnormal K+ <3.5 mmol/lit will be given a single bolus. Each bolus will be given for one hour apart and after the required boluses given then ABG`s and S/E will be performed one hour afte
200ml/kg/day of 5% dextrose in 0.45% saline with the addition of potassium dependent on the patient&#39
s potassium level until adequate resuscitation will be achieved. ABGS and S/E will be accessed every 8 hourly.
Active Comparator Other,Active Comparator Other
Bolus fluid therapy,Conventional fluid therapy

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Weeks to 8 Weeks

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Time to preoperative optimization After start of either conventional or bolus fluid therapy hours

Secondary

MeasureTime frame
Hospital Stay at the time of discharge hours

Countries

Pakistan

Contacts

Public ContactMuhammad Salman Saleem

Department of Pediatric Surgery, The Children&#039;s Hospital and the Institute of Child Health, Lahore

salman_10@hotmail.com00923352757000

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026