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NCT03015610CompletedPhase 3

Genotype-tailored Treatment of Symptomatic Acid-Reflux in Children With Uncontrolled Asthma

Source: ClinicalTrials.gov · Last updated 9 Sept 2025

Brief summary (registry, in English)

This study will evaluate the effect of CYP2C19 and ABCB1 genes on pharmacokinetics of lansoprazole in children with mild gastroesophageal reflux (GER) and uncontrolled asthma. It will determine if genotype-guided lansoprazole dosing of lansoprazole improves GER and asthma control.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
41 (actual)
First submitted
13 Dec 2016
Start date
31 Oct 2017
Primary completion date
18 Jan 2024
Lead sponsor
Jason Lang, M.D., M.P.H.
Diseases
Asthma
NCT number
NCT03015610

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 41
  • From 31 Oct 2017 to the primary completion date, 18 Jan 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Taking daily CYP2C19 substrates, inducers or inhibitors medication
  • Past or current history of moderate-severe GERD or related disorders (erosive esophagitis, peptic ulcer disease, eosinophilic esophagitis) which in the opinion of the pediatric gastroenterology safety specialist/study physician requires treatment with acid-blocking agents;
  • previous intubation for asthma,
  • Previous surgery involving the esophagus or stomach (anti-reflux surgery, peptic ulcer surgery, trachea-esophageal fistula repair);
  • Medication use: treatment of GERD symptoms with over-the-counter antacids 4 days/week or more on average over past month;
  • Any investigational drugs within the past 2 months;
  • Drug Allergies: previous allergic reaction from lansoprazole or other proton pump inhibitor medication or adverse reaction to aspartame;
  • Less than 75% completion of daily diary for asthma symptoms, SABA use and ICS medication adherence during the run-in period;

Other illness

  • Any major chronic illness that would interfere with participation in the intervention or completion of the study procedures;
  • History of phenylketonuria (PKU);
  • Theophylline preparations, azoles, anti-coagulants, insulin for Type 1 diabetes, digitalis, oral iron supplements when administered for iron deficiency within 1 month;

Other

  • Daily use of a PPI for more than 4 consecutive weeks in the past 6 months;
  • admission to intensive care unit for more than 24 hours for asthma in the past year,
  • Forced expiratory volume in 1 second (FEV1) \< 60% of predicted at enrollment;
  • Inability to complete baseline measurements in a satisfactory manner according to the judgment of the research coordinator or site PI;
  • Plan for family to move from study location within the next 6 months.

Who the study is looking for

  • Age: 6-17 year olds with documented clinician-diagnosed asthma
  • Evidence of recent uncontrolled asthma (must meet at least one of the following). This convention for defining poorly-controlled asthma has been successfully used in a large pediatric trial.
    • ACQ \> 1.2
    • Use of short-acting beta-agonist for asthma symptoms twice/week or more on average over the past month
    • Nocturnal awakenings with asthma symptoms more than once per week on average over the last month
    • Two or more emergency department visits, unscheduled provider visits, prednisone courses or hospitalizations for asthma in the past 12 months
  • Currently on stable dose of daily inhaled corticosteroid medication (ICS) for asthma control equivalent to 88mcg of fluticasone or greater for at least 6 weeks from the time of enrollment. Participant must be on National Asthma Education and Prevention Program (NAEPP) controller step 2, 3 or 4.
  • Currently with mild GERD symptoms reported at V1 defined by a score on the Pediatric GERD Symptom Assessment Score greater than 15 and less than 80. GSAS ranges from 0 to \>440.

Age in the registry: 6 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Duke University Medical Center
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status
Nemours Children's Specialty Care
Coordinator of this site? Confirm its status
JacksonvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.