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Prospective, Comparative, Randomized, Controlled Trial on the Efficacy of the Treatment of Gastroesophageal Reflux Infant With Magnesium Alginate

Prospective, Comparative, Randomized, Controlled Trial on the Efficacy of the Treatment of Gastroesophageal Reflux Infant With Magnesium Alginate

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01858584
Enrollment
75
Registered
2013-05-21
Start date
2013-02-28
Completion date
Unknown
Last updated
2013-05-30

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

Conditions

Chronic Cough, Gastroesophageal Reflux, Regurgitation, Vomiting

Keywords

GER, Alginate, Regurgitation, questionnaire

Brief summary

The results on the efficacy of the formulations based on alginic acid are controversial. Corvaglia et al demonstrated a significant reduction in reflux episodes in preterm infants by evaluation with pH-impedance analysis. This study concludes that the use of alginic acid reduces the acidity of the gastroesophageal reflux (GER) and has a non-systemic effect and a lesser presence of side effects compared to the use of H2-receptor antagonist(H2RA) and proton pump inhibitor (PPI).

Detailed description

Primary outcomes This prospective, randomized, controlled trial aims to determine, in a population of infants within one year of life, suffering from gastroesophageal reflux (GER) the effectiveness of magnesium alginate. The clinical improvement of the patient will be evaluated based on the negativity of the symptom score (4.3.1), assessed using a validated questionnaire on symptoms of GER (I-GERQ Annex A). Secondary outcomes To compare the efficacy of Magnesium Alginate on GER in infants compared with those of thickened feeding and reassurance, basing on questionnaire results.

Interventions

DRUGGastrotuss

Gastrotuss baby: syrup based on alginate consisting of: magnesium alginate, simethicone, fructose, xanthan gum, honey, D-panthenol, fluid extracts of Althaea officinalis, Papaver rhoeas, zinc oxide, sodium bicarbonate, sodium hydroxide, p-hydroxybenzoate of methyl-sodium, sodium propyl p-hydroxybenzoate, natural flavors, erythrosine (E127), purified water. dosage: * Infants weighing \<5 kg in 2.5 ml 5-10 min after feeding. In case of regurgitation after administration, 1 ml additional * Infants weighing\> 5 kg per 5 ml dose after the meal and the evening before putting the baby to sleep The administration should be maximum 3 times per day

DIETARY_SUPPLEMENTthickened milk

Milk thickened (formulat AR): contains a special thickener derived from corn starch waxy, that maintains its fluidity into the bottle and thickens just inside the stomach of the child, and this makes it easy to use in breastfeeding , as it is usable with a common teat.

Sponsors

Federico II University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
No minimum to 12 Months
Healthy volunteers
No

Inclusion criteria

* Age \< 1 year * Suggestive symptoms of gastroesophageal reflux (I-GERQ score \> 7) * Absence of clinical evidence of allergy to cow milk protein or other allergic disorder * No previous intake of thickened formulas, acid suppressants or drugs * All parents or guardians must sign a document of informed consent * Patients affected by chronic disease * Patients affected by hepatic or renal diseases * Patients affected by cardiac diseases

Exclusion criteria

* Patients affected by chronic disease * Patients affected by hepatic or renal diseases * Patients affected by cardiac diseases * Inability or unwillingness to give informed consent * Patients wth severe neurologic disease * Patients affected by cow milk protein allergy * Previous or ongoing intake of thickened formulas, acid suppressants or drugs

Design outcomes

Primary

MeasureTime frameDescription
efficacy on GER2 monthsThis prospective, randomized, controlled trial aims to determine, in a population of infants within one year of life, suffering from RGE the effectiveness of magnesium alginate. The clinical improvement of the patient will be evaluated based on the negativity of the symptom score (4.3.1), assessed using a validated questionnaire on symptoms of GER (I-GERQ Annex A).

Secondary

MeasureTime frameDescription
comparison of treatments2 months• To compare the efficacy of Magnesium Alginate on GER in infants compared with those of thickened feeding and reassurance.

Countries

Italy

Contacts

Primary ContactAnnamaria Staiano
staiano@unina.it+39 081 7462669

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026