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Fexuprazan for the reducing upper gastrointestinal risk in patients with acute ischemic stroke and gastroesophageal reflux disease

Fexuprazan for the reducing upper gastrointestinal risk in patients with acute ischemic stroke and gastroesophageal reflux disease: a prospective single-arm observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008578
Enrollment
20
Registered
2023-06-28
Start date
2023-07-08
Completion date
Unknown
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Yonsei University Yongin Severance Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adults aged 19 years or older. 2) Patients hospitalized for acute ischemic stroke within 7 days of symptom onset, confirmed through Brain CT or MRI. 3) Patients who are receiving antithrombotic treatment. 4) Patients with a Gastroesophageal Reflux Disease Questionnaire (GerdQ) score of 8 or higher at the time of screening. 5) Patients who are receiving treatment with Fexuprazan. 6) Individuals who have voluntarily provided written informed consent to participate in this clinical trial.

Exclusion criteria

Exclusion criteria: 1) Patients who have undergone intravenous thrombolysis and/or intra-arterial thrombectomy for the treatment of ischemic stroke. 2) Individuals who have had an allergic reaction to Fexuprazan. 3) Patients who are unable to complete the GerdQ questionnaire. 4) Pregnant or breastfeeding individuals. 5) Individuals who have participated in another drug clinical trial within the past month, except for observational studies, in which case participation in this clinical trial is allowed. 6) Individuals whom the investigator deems inappropriate for participation in the clinical trial for other reasons.

Design outcomes

Primary

MeasureTime frame
Gastroesophageal reflux disease questionnaire (GerdQ)

Secondary

MeasureTime frame
Clinical event of upper gastrointestinal complications as a complication of gastroesophageal reflux disease.

Countries

Korea, Republic of

Contacts

Public ContactJeonga Shin

Yonsei University Yongin Severance Hospital

ja61236@yuhs.ac+82-31-5189-8160

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026