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Status unknownNCT01159509Updated Jul 9, 2010

The Effect of Hypertrophic Pyloric Stenosis (HPS) on Sodium Intake in Childhood

An observational study in Healthy and Hypertrophic Pyloric Stenosis, sponsored by Sheba Medical Center. Status unknown. Open to participants aged 7 Years to 13 Years. Per ClinicalTrials.gov, last updated 2010-07-09.

Sponsored by Sheba Medical Center · Observational

The sponsor has not verified this record recently (last verified Jul 2010), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
40
Ages
7 Years to 13 Years
Sex
All
01

Study summary

The loss of sodium during infancy causes long term changes in sodium intake. Human research shows that the loss of maternal sodium during pregnancy and neonatal after birth causes an increase sodium intake during childhood. A study that examined sodium intake among infants that were treated with diuretics during the post-natal period found changes in sodium intake compared to controls. In this study we will test sodium intake in young children who have suffered from vomiting due to Hypertrophic Pyloric stenosis during early infancy.

02

Conditions studied

  • Healthy
  • Hypertrophic Pyloric Stenosis

Keywords

  • hypertrophic pyloric stenosis
  • sodium intake
  • Healthy children with no chronic diseases
  • Status post HPS
03

In context

Pyloric Stenosis

29 studies on the registry are indexed under Pyloric Stenosis; 1 is open to participants now.

Browse Pyloric Stenosis studies →

Lead sponsor

Sheba Medical Center is the lead sponsor of 660 studies on the registry; 63 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 13 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children ages 7-13 years. Status post HPS in infancy

Inclusion criteria

  • Children ages 7-13 years
  • Status post HPS in infancy

Exclusion criteria

Exclusion Criteria:

  • Children with chronic diseases
  • Hospitalization due to dehydration after HPS hospitalization
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
40 participants (estimated)

Groups and cohorts

  • Infants ages -13 years that had HPS in infancy

    Behavioral: sodium taste tests

Interventions

  • Behavioralsodium taste tests

    The cohort group will had sodium taste tests and an interview regarding diat habits.

06

What researchers measure

Primary outcomes

  1. Increased sodium intake

    Time frame: 1 year

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01159509
Lead sponsor
Sheba Medical Center
Collaborators
University of Haifa
First posted
Jul 9, 2010
Start date
Sep 2010
Primary completion
Jul 2011 (estimated)
Completion
Jul 2011 (estimated)
Last update
Jul 9, 2010

Study contacts

Ayala Maayan-Metzger, Dr.
Contact
972-54-6278248

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2010. You cannot join it, but the record below documents what was studied.

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