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NCT04454112

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

Completed NA Last updated 1 July 2020
What this trial tests

NA trial testing 24-hour esophageal pH monitoring using an ambulatory system (Ohmega, MMS, Enschede, The Netherlands). in Gastroesophageal Reflux in 20 participants. Completed in 12 December 2018.

Timeline
12 March 2018
Primary endpoint
12 December 2018
12 December 2018

Quick facts

Lead sponsorFatma Demirbaş
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment20
Start date12 March 2018
Primary completion12 December 2018
Estimated completion12 December 2018
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Fatma Demirbaş

Who can join

Eligibility, any sex, with Gastroesophageal Reflux. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Gastroesophageal Reflux

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04454112.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing