MedTrace Logo

Pre and Post-gastrostomy Evaluation of GER in Children Using 24-hour pH Monitoring

NCT04454112 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-07-01

No results posted yet for this study

Summary

The aim of this study was to evaluate 24-hour pH monitoring results before and after gastrostomy in neurological impaired (NI) children who underwent gastrostomy or Nissen fundoplication (NF) concurrently with gastrostomy.

Conditions

  • Gastroesophageal Reflux

Interventions

DEVICE

24-hour esophageal pH monitoring using an ambulatory system (Ohmega, MMS, Enschede, The Netherlands).

24-hour esophageal pH monitoring application

Sponsors & Collaborators

  • Fatma Demirbaş

    lead OTHER

Principal Investigators

  • Berat Dilek Demirel · she underwent gastrostomy to patients with neurological damage

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-12
Primary Completion
2018-12-12
Completion
2018-12-12

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04454112 on ClinicalTrials.gov