Heartburn

5

Review clinical trials related to Heartburn. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Antireflux Surgery Without Preoperative Esophageal Manometry

The goal of this clinical trial is to learn if people can safely skip a test called esophageal manometry before surgery for acid reflux (gastroesophageal reflux disease, or GERD) or a hiatal hernia. Manometry measures the muscles of the food pipe using a thin tube passed through the nose. The test can be uncomfortable and can delay surgery. The main questions this study aims to answer are whether people can skip manometry and still have good swallowing one year after surgery, and whether skipping the test lowers discomfort, shortens the wait for surgery, and lowers cost. To answer this, researchers will compare two groups. One group will have surgery without manometry. The other group will have manometry first, the way it is usually done. Everyone will get the same operation, a partial wrap called a Toupet fundoplication, so the study tests the value of the test and not the surgery. Participants will be placed by chance into one of the two groups, have the same standard operation, and fill out short questionnaires about their swallowing before surgery and again at 3, 6, and 12 months after surgery. Researchers want to find out if skipping manometry works just as well as the usual approach for people who do not have trouble swallowing before surgery.

Participants needed: 96
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: McMaster UniversityUpdated: Jun 22, 2026Locations: 2
Eligibility criteria

Age ≥ 18 years [+9]

Overt dysphagia (Mellow-Pinkas ≥ 1 or Eckardt ≥ 1) [+10]

Status: Recruiting

Domperidone in Treating Patients With Gastrointestinal Disorders

This phase III trial studies how well domperidone works in treating patients with gastrointestinal disorders. Domperidone may help control chronic gastrointestinal disorders and their symptoms, such as pain, bloating, and nausea and vomiting, by stimulating contraction of the stomach to increase its ability to empty itself of food.

Participants needed: 200
Trial details
Phase: Phase 3Age: 16+Biological sex: AllType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Patients with GI disorders who have failed standard therapy [+13]

Patients with the following cardiac diagnoses: ventricular tachycardia or fibril... [+8]

Status: Recruiting

A Study of Breath Testing for Small Intestinal Bacterial Overgrowth

Researchers hope to determine how often small intestinal bacterial overgrowth occurs after taking proton pump inhibitors.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Feb 12, 2026Locations: 1
Eligibility criteria

Predominant symptoms of gastroesophageal reflux disease including heartburn, reg... [+1]

Prior diagnosis of SIBO [+8]

Status: Recruiting

A Study of the Safety of Vonoprazan Exposure in Pregnant Women and Their Offspring

The main objective of the study is to compare the maternal, fetal, and infant outcomes of pregnant women who are exposed to vonoprazan during pregnancy with outcomes of an internal comparison cohort of pregnant women who are unexposed to vonoprazan during pregnancy but who may be exposed to other products for the treatment of conditions for which vonoprazan may be prescribed.

Participants needed: 728
Trial details
Age: 15-50Biological sex: FemaleType: ObservationalSponsor: Phathom Pharmaceuticals, Inc.Updated: May 22, 2025Locations: 1Duration: 12 Months
Eligibility criteria

Women 15 to 50 years of age. [+5]

Occurrence of pregnancy outcome prior to first contact with the virtual research... [+2]

Status: Recruiting

Comparative Pharmacodynamics and Pharmacodynamics Equivalence of Antareit 800 mg/10 ml Oral Suspension and Riopan 800 mg Chewable Tablets in Healthy Volunteers

Comparative study of the pharmacodynamic parameters and pharmacodynamic equivalence (bioequivalence) of drug Antareit 800 mg/10 ml oral suspension and drug Riopan 800 mg chewable tablets in healthy volunteers.

Participants needed: 50
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Valenta Pharm JSCUpdated: Jul 22, 2024Locations: 2
Eligibility criteria

Voluntary and handwritten informed consent form signed by a healthy volunteer to... [+9]

A history of allergy; [+37]