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Gastroesophageal reflux disease in infants is not fully understood. Infants are prescribed medical treatments that may not be effective or that contribute to adverse side effects and lead to concerns and expenses for the parents and healthcare system. Current guidelines recommend cow-milk-protein free diet as a first-line treatment, but these recommendations are based on weak evidence. This study investigate the efficacy of a cow-milk-protein free diet compared to treatment with a proton pump inhibitor (omeprazole)
An increasing number of infants less than one year of age have been referred to the pediatric departments with gastroesophageal reflux in the past decade. Gastroesophageal reflux is a common condition in infants defined as the passage of gastric contents into the esophagus with regurgitation or vomiting. Around 50% of infants younger than four months regurgitate or vomit regularly. In most cases, it is a harmless, self-limiting condition; in 90% of cases, the symptoms diminish before 12 months. However, if reflux leads to troublesome symptoms or complications, it is defined as gastroesophageal reflux disease. Troublesome symptoms may include failure to thrive, back arching, food refusal, regurgitation, and irritability. The prevalence of gastroesophageal reflux disease varies between studies. Infants can be treated medically, and proton pump Inhibitors have been recommended as the first choice. However, within the last few years, there has been concern among pediatricians that too many infants are unnecessarily treated with this medication. There are only a few randomized studies on proton pump inhibitor treatment in children under one year, and most studies do not show a significant effect on symptoms. Side effects of treatment with proton pump inhibitors include symptoms related to the gastrointestinal tract or airways, increased susceptibility to infections, and increased risk of developing allergy later in life. Within the past years, there has been attention to the overlapping of symptoms between gastroesophageal reflux disease and allergy to cow milk protein. Cow-milk-protein allergy is the most common food allergy in early childhood, with an estimated prevalence of 2-3%, and presents with various symptoms predominantly from the skin and gastrointestinal tract. Consequently, cow-milk-protein allergy can be challenging to differentiate from gastroesophageal reflux disease. Cow-milk-protein-allergy is an immune reaction and can be either immunoglobulin E-mediated, presenting with immediate reaction including anaphylaxis, or non-immunoglobulin E-mediated, presenting with delayed symptoms. In addition, it is possible that cow's milk can aggravate gastroesophageal reflux disease with a non-immunologic mechanism. As there is no biomarker to differentiate non-immunoglobulin E-mediated cow-milk allergy from gastroesophageal reflux disease, the diagnosis of non-immunoglobulin E-mediated cow-milk allergy can only be verified by an oral food challenge test preceded by a cow-milk-protein-elimination period. Therefore, in the updated international guidelines, all children with gastroesophageal reflux disease should start with a 2-4-week cow-milk-protein-elimination diet before a proton pump inhibitor is prescribed. However, evidence is scarce on the effect of a cow-milk-protein-free diet in infants diagnosed with gastroesophageal reflux disease.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Proton pump inhibitor | Active Comparator | Omeprazole 1 mg/ kg and continuing nutrition containing cow's milk protein |
|
| Mother or infant diet | Active Comparator | Mother on cow milk-protein-free diet if breastfeeding and infant on a hypoallergenic formula if bottle-fed. |
|
| Placebo | Placebo Comparator | Placebo medicine (appearing substantially like Omeprazole) 1mg/kg and continuing nutrition containing cow's milk protein |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Protein pump inhibitor. | Drug | 1 mg/kg /day |
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| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in reflux episodes in the fourth week of active treatment, compared to placebo | Parent-reported reduction in the weekly number of reflux-episodes in the fourth week of active treatment with either PPI or diet, compared to placebo. The outcome is registered daily in an App. | Baseline and daily in 4 weeks. |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in reflux episodes in the fourth week in the PPI group, compared to the diet group. | Reduction in the number of regurgitation episodes (compared to the run-in period) in the PPI group compared to the diet group | Baseline and 4 weeks |
| Change from baseline in weight |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events to trial medicine in the proton pump inhibitor group and the placebo group | Any parent-reported adverse events to the trial medicine (both Omeprazole and placebo) are registered weekly. There are several well-known side effects; 1-10 % experience symptoms from the gastrointestinal tract (i.e., stomach pain, nausea, and constipation), skin, airways, and increased susceptibility to infections. |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Natalia K Barkholt, MD | Contact | +4521787136 | Natalia.Barkholt@rsyd.dk | |
| Gitte Zachariassen, Professor | Contact | +4565413809 | Gitte.Zachariassen@rsyd.dk |
| Name | Affiliation | Role |
|---|---|---|
| Gitte Zachariassen, Professor | H.C Andersen Childrens Hospital, Odense University Hospital and Syddansk University (SDU) | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Paediatric Department, Hospital of Southern Jutland | Recruiting | Aabenraa | Region Syddanmark | 6200 | Denmark |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41612404 | Derived | Barkholt NK, Dalby K, Mogensen CB, Zachariassen G, Gradman J. Infant Reflux Trial: study protocol for a multicentre randomized controlled trial on the treatment of gastroesophageal reflux disease in infants. Trials. 2026 Jan 29;27(1):169. doi: 10.1186/s13063-026-09477-x. |
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Raw data can not be shared, but the study protocol and the Statistical Analysis plan will be shared.
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| ID | Term |
|---|---|
| D005764 | Gastroesophageal Reflux |
| D007232 | Infant, Newborn, Diseases |
| ID | Term |
|---|---|
| D015154 | Esophageal Motility Disorders |
| D003680 | Deglutition Disorders |
| D004935 | Esophageal Diseases |
| D005767 | Gastrointestinal Diseases |
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| ID | Term |
|---|---|
| D009853 | Omeprazole |
| ID | Term |
|---|---|
| D053799 | 2-Pyridinylmethylsulfinylbenzimidazoles |
| D013454 | Sulfoxides |
| D013457 | Sulfur Compounds |
| D009930 | Organic Chemicals |
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The study is partially blinded. There is blinding in relation to the placebo arm and the proton pump inhibitor arm.
| Mother or infant diet | Behavioral | Mother on cow milk protein diet or infant on hypoallergenic formula in case of bottle fed |
|
|
| Placebo | Drug | Placebo medicine (appearing substantially like Omeprazole) 1mg/ ml, and continuing nutrition containing cows' milk protein |
|
A nurse or physician will perform the measurement on a weight in the clinic/hospital. Measurement unit: gram. |
| Baseline and 4 weeks |
| Change from baseline in the number of reflux episodes with visible blood | Parent reported weekly number of reflux episodes with visible blood. Registered in MyCap App. | 1,2,3,4 weeks |
| Change from baseline in the number of episodes with discomfort | Parent reported weekly episodes with discomfort 5 minutes after feeding. Registered in MyCap App | 1,2,3,4 weeks |
| Change from baseline in the numbers of episodes with crying | Parent reported weekly numbers of episodes with crying 5 minutes after feeding. Registered in MyCap App | 1,2,3,4 weeks |
| Change from baseline in the number of episodes of refusing breast/ bottle | Parent reported weekly numbers of episodes of refusing breast/bottle. Registered in MyCap App | 1,2,3,4 weeks |
| Change from baseline in the number of episodes with short breathing pauses | Parent-reported weekly numbers of episodes with short breathing pauses. Registered in MyCap App | 1,2,3,4 weeks |
| Change from baseline in the number of episodes with paleness/blue color in face or lips | Parent reported weekly numbers of episodes with paleness/blue color in face. Registered in MyCap App | 1,2,3,4 weeks |
| Change from baseline in the number of episodes with troublesome breathing/cough | Parent reported weekly numbers of episodes with troublesome breathing/cough. Registered in MyCap App | 1,2,3,4 weeks |
| Immunoglobulin E level | Blood positive/negative for specific immunoglobulin E for cows milk protein. Values above 0,35 kU/l are considered positive for cows' milk allergy. | 4 weeks after treatment is started |
| 1,2,3,4 weeks |
| Cows milk allergy? | After 4 weeks´ of cows milk protein-free diet, an oral provocation test with cow's milk is conducted on all infants in the diet group, who experienced effect of the diet. The test will be carried out in the hospital. During the test, the infants are given increasing doses of fresh cow's milk every 30 minutes until they reach a maximum of 200 ml. A nurse records any symptoms experienced during the first few hours of the test, and the parents are required to monitor and report any symptoms at home. Additionally, the parents inform the physician of any late symptoms via phone call 48 hours after the test. | 4 weeks |
| Børnelægecentret v/Kasper Dalby | Not yet recruiting | Odense | Region Syddanmark | 5000 | Denmark |
|
| H.C Andersen Childrens' Hospital | Not yet recruiting | Odense | Region Syddanmark | 5000 | Denmark |
|
| D004066 | Digestive System Diseases |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D011725 |
| Pyridines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D001562 | Benzimidazoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |