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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04720781
Other study ID # Revisiting
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 21, 2021
Est. completion date December 31, 2024

Study information

Verified date February 2024
Source Showa Inan General Hospital
Contact Akira Horiuchi, MD
Phone 81265822121
Email horiuchi.akira@sihp.jp
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

After vonoprazan (20mg/day) or esomeprazole (20mg/day) for 4weeks is prescribed for patients with erosive esophagitis diagnosed by esophagogastroduodenoscopy, the number of patients who will visit our outpatient clinic again due to some reasons without any appointments is compared with vonoprazan group and esomeprazole.


Description:

1. Patients who have erosive esophagitis diagnosed by esophagogastroduodenoscopy is enrolled. 2. Vonoprazan (20mg/day) or esomeprazole (20mg/day) is prescribed for 4weeks the patients randomly without next appointments. 3. Some patients may visit our outpatient clinic again due to some reasons without any appointments. 4. The number of the patients who revisit our outpatient clinic again is compared with vonoprazan group and esomeprazole.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years to 100 Years
Eligibility Inclusion Criteria: - outpatients belonging to American Society of Anesthesiologists class I or II - patients have erosive esophagitis diagnosed by esophagogastroduodenoscopy shortly before the prescription Exclusion Criteria: - other acid blockers are taken

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Vonoprazan
Vonoprazan (20mg/day) is prescribed for 4 weeks.
Esomeprazole
esomeprazole (20mg/day)

Locations

Country Name City State
Japan Showa Inan General hospital Komagane Nagano

Sponsors (1)

Lead Sponsor Collaborator
Showa Inan General Hospital

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Other Questionnaire on satisfaction with taking the medicine at revisiting The patient's satisfaction is assessed using visual analogue scale (Exellent 100% to very bad 0%). 3months
Primary The number of patients who revisit our outpatient clinic after the prescription without any appointments The need to revisit our outpatient clinic again without any appointments may show the patients' satisfaction or dissatisfaction after the prescription of vonoprazan or esomeprazole. The difference in the number between the two groups may show the difference in the effectiveness between the two medicines. 3 months
Secondary Change of the main symptom with patients after/before medication when the patients revisit again The ratio of the degree of the main symptom after/before taking the medicine Good 0%- Bad 100% 3 months
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