known hypertensive patients admitted to emergency department with increased blood pressure will be evaluated in terms of antihypertensive agents given at hospital, degree of blood pressure decrease, hospital stay and laboratory and imaging tests ordered. The impact of routine oral antihypertensive agents used by the patients on these parameter will be assessed.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
1. Patients aged 18 and older.
2. Blood pressure measured at ≥140/80.
3. Diagnosis of essential hypertension.
Exclusion Criteria:
1. Pregnant patients.
2. Individuals without a prior diagnosis of hypertension.
3. Patients with end-organ damage (hypertensive emergency).
4. Patients whose routine antihypertensive agents are unavailable.
5. Patients who leave the clinic without permission, making follow-up data inaccessible.
Primary outcome measure(s)
routine use of oral antihypertensive agents and its effects on emergency service care — from enrollment to the end of follow up duration of 7 days emergency service blood pressure target achievement duration changes depending on routine oral antihypertensive agent prescribed
Trial sites (2)
Facility
City
Region
Status
Etlik City Hospital
Ankara
Turkey (Türkiye)
Etimesgut Military Hospital
Ankara
Turkey (Türkiye)
More Saglik Bilimleri Universitesi trials in Turkey
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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