Skip to content

Clinical study of sensory evaluation using Olmesartan orally disintegrating tablet (OD tablets) for hypertensive patients.

Clinical study of sensory evaluation using Olmesartan orally disintegrating tablet (OD tablets) for hypertensive patients. - Clinical study of sensory evaluation using Olmesartan orally disintegrating tablet (OD tablets) for hypertensive patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019202
Enrollment
30
Registered
2015-10-01
Start date
2015-10-13
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Hypertension

Interventions

Hypertensive patients using Olmesartan tablets 20mg take Olmesartan OD tablets 20mg.Intervention period : 1 day

Sponsors

Medical corporation Ishinkai Oda clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who are 20 years of age or older at the moment obtaining informed consent. 2) Patients who are already taking Olmesartan tablets 20mg from before more than two weeks of obtaining informed consent. 3) Patients who provided voluntary informed consent to participate in the study after receiving sufficient explanation.

Exclusion criteria

Exclusion criteria: 1) Patients who are taking dementia therapeutics. 2) Patients who are a history of hypersensitivity to Olmesartan tablet. 3) Diabetic patients who are taking aliskiren fumarate(Except for uncontrolled patients of blood pressure by doing other antihypertensive treatment.) 4) Patients who are pregnant or during lactation, or there is becoming the possibility of pregnant. 5) Patients who jugged unsuitable for this study by the investigator.

Design outcomes

Primary

MeasureTime frame
Evaluation of sensory

Secondary

MeasureTime frame
Evaluation of safety

Countries

Japan

Contacts

Public ContactKotaro Senuki

Sogo Rinsho Médéfi Co,Ltd. Business Promotion Department

OLM-OD@sogo-medefi.jp03-6901-6079

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026