New heartburn pill may change how blood thinners work after stent placement
NCT ID NCT07471867
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a new drug called ZaStaprazan affects how well the blood thinner clopidogrel works in people who have had a heart procedure (stent placement). About 100 adults with chronic coronary syndrome will take either ZaStaprazan or a standard heartburn drug (PPI) for one month. The main goal is to measure blood clotting activity to see if ZaStaprazan is a safer option for managing stomach acid without interfering with heart medication.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Jul 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 19 years or older at the time of providing informed consent. 2. Patients with Chronic Coronary Syndrome (CCS) who have undergone Percutaneous Coronary Intervention (PCI) and agreed to participate in the study. 3. Patients who are required to maintain dual antiplatelet therapy (DAPT) including clopidogrel for at least 6 months after PCI. 4. Patients who have voluntarily provided written informed consent to participate in this clinical study. Exclusion Criteria: 1. History of hypersensitivity to P-CABs, PPIs, benzimidazoles, aspirin, clopidogrel, or any of the excipients in the study drugs. 2. History of or planned surgery that may affect gastric acid secretion, such as upper gastrointestinal resection, acid suppression surgery, or gastric mucosal resection. (However, patients who have undergone simple perforation repair of the stomach or duodenum, appendectomy, cholecystectomy, hysterectomy, or endoscopic/laparoscopic resection of benign tumors are eligible). 3. Diagnosis of Zollinger-Ellison syndrome or inflammatory diseases (e.g., pancreatitis, or inflammatory bowel diseases such as Crohn's disease or ulcerative colitis). 4. Currently receiving HIV protease inhibitors (atazanavir, nelfinavir) or rilpivirine-containing products. 5. Abnormal blood chemistry values within 4 weeks prior to screening: AST, ALT, ALP, or total bilirubin \> 3 times the upper limit of normal (ULN). Estimated Glomerular Filtration Rate (eGFR) \< 30 mL/min/1.73m², calculated using the IDMS-traceable MDRD equation. 6. Recent Medication Use: Use of medications expected to affect the study results, such as P2Y12 inhibitors (other than the prescribed clopidogrel), within 2 weeks prior to baseline. 7. Pregnant or lactating women, or women with a positive pregnancy test. 8. Patients with hereditary problems such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Yongin Severance Hospital, Yonsei University
RECRUITINGYongin-si, Gyeonggi-do, 16995, South Korea
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a shorter course of two blood thinners keep stents safe?
- Can a shorter course of blood thinners work after Metal-Free heart balloons?
- A 7,000-Person trial asks: is lifelong aspirin necessary for older hearts?
- Can a higher dose of adenosine sharpen heart scans?
- Can a trained eye match ultrasound for heart stent placement?