Clinical Trial for the Comparative Evaluation of Acid Suppression and Symptom Management of Gastroesophageal Reflux Disease With the Administration of Tegoprazan or Pantoprazole
Recruiting
Phase 4Interventional Study
Gastroesophageal Reflux Disease
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
128 (estimated)
Sponsor
Carnot Laboratories · Industry
Who this trial is looking for
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The objective of this clinical trial is to compare which of the two drugs best resolves symptoms in patients diagnosed with erosive and non-erosive gastroesophageal reflux disease, adult males and females. The main question is What is the proportion of patients with resolution of the main symptoms of gastroesophageal reflux disease at four weeks of treatment with pantoprazole vs tegoprazan.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* With endoscopic diagnosis of GERD or NERD (endoscopy ≤ 15 days old)
* With positive impedance pHmetry results (pHmetry ≤ 15 days old)
* With recurrent symptoms of heartburn and regurgitation for a previous period ≥ 3 months old
Exclusion Criteria:
* With known hypersensitivi…
Inclusion Criteria:
* With endoscopic diagnosis of GERD or NERD (endoscopy ≤ 15 days old)
* With positive impedance pHmetry results (pHmetry ≤ 15 days old)
* With recurrent symptoms of heartburn and regurgitation for a previous period ≥ 3 months old
Exclusion Criteria:
* With known hypersensitivity to tegoprazan, pantoprazole, or any of the components of each formulation
* Subjects with concomitant administration of atazanavir, nelfinavir or rilpivirine
* Nephropathic and/or hepatopathic subjects (including non-alcoholic hepatitis)
* Subjects with upper gastrointestinal tract bleeding
* Subjects with gastric and/or duodenal ulcer 2 months prior to screening
* Subjects with a history of esophageal or gastric surgery
Contacts
No contact information available.
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