Hypertension Management in Terms of Routine Agents

NCT06635616 | Not Yet Recruiting

• 1 other identifier: hypertension
• Study Type: observational
• Target: 350
• Locations: 1 country
• Sites: 2

Brief Summary

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.

Conditions

Hypertension; Emergency Medicine

Keywords

hypertension; emergency medicine; oral antihypertensive agents

Outcome Measures

Primary Outcomes (1)

• routine use of oral antihypertensive agents and its effects on emergency service care

  emergency service blood pressure target achievement duration changes depending on routine oral antihypertensive agent prescribed

  from enrollment to the end of follow up duration of 7 days

Study Arms (6)

diuretics

patients prescribed diuretics for oral treatment admitted to emergency service with elevated blood pressure

Beta Blockers

patients prescribed Beta Blockers for oral treatment admitted to emergency service with elevated blood pressure

Calcium Channel Blockers

patients prescribed Calcium Channel Blockers for oral treatment admitted to emergency service with elevated blood pressure

ACE (angiotensin converting enzyme) Inhibitors

patients prescribed ACE (angiotensin converting enzyme) Inhibitors for oral treatment admitted to emergency service with elevated blood pressure

ARB( angiotensin receptor blockers)

patients prescribed ARB( angiotensin receptor blockers) for oral treatment admitted to emergency service with elevated blood pressure

combination

patients prescribed combination agents for oral treatment admitted to emergency service with elevated blood pressure

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

patients with known hypertension admitted to emergency department with elevated blood pressure

You may qualify if:

• Patients aged 18 and older.
• Blood pressure measured at ≥140/80.
• Diagnosis of essential hypertension.

You may not qualify if:

• Pregnant patients.
• Individuals without a prior diagnosis of hypertension.
• Patients with end-organ damage (hypertensive emergency).
• Patients whose routine antihypertensive agents are unavailable.
• Patients who leave the clinic without permission, making follow-up data inaccessible.

Sponsors & Collaborators

• Saglik Bilimleri Universitesi: lead
• Etimesgut Military Hospital: collaborator

Study Sites (2)

Etlik City Hospital

Ankara, 06170, Turkey (Türkiye)

Location

Etimesgut Military Hospital

Ankara, 06790, Turkey (Türkiye)

Location

Related Publications (3)

• Salvetti M, Paini A, Colonetti E, Tarozzi L, Bertacchini F, Aggiusti C, Stassaldi D, Rosei CA, Rosei EA, Muiesan ML. Hypertensive emergencies and urgencies: a single-centre experience in Northern Italy 2008-2015. J Hypertens. 2020 Jan;38(1):52-58. doi: 10.1097/HJH.0000000000002213.

  PMID: 31415308 BACKGROUND

• Nowicki J, Silka W, Zalustowicz A, Rajzer M, Olszanecka A. Uncontrolled hypertension and hypertensive urgency: One-year single-center emergency department experience. Kardiol Pol. 2024;82(4):407-415. doi: 10.33963/v.phj.100025. Epub 2024 Apr 12.

  PMID: 38606743 BACKGROUND

• Astarita A, Covella M, Vallelonga F, Cesareo M, Totaro S, Ventre L, Apra F, Veglio F, Milan A. Hypertensive emergencies and urgencies in emergency departments: a systematic review and meta-analysis. J Hypertens. 2020 Jul;38(7):1203-1210. doi: 10.1097/HJH.0000000000002372.

  PMID: 32510905 BACKGROUND

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular Diseases; Cardiovascular Diseases

Study Officials

• Elif HAMZACEBIOGLU KAYISOGLU, Specialist

  Etimesgut Military Hospital

  STUDY DIRECTOR

• Gulsen AKCAY, Ass. Prof.

  Ankara Etlik City Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Gulsen AKCAY, Ass. Prof.

CONTACT

+905052874949; gulakcay@yahoo.com.tr

Elif HAMZACEBIOGLU KAYISOGLU, Specialist

CONTACT

+905453300679; turkuaz-61@indowslive.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 30 Days
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 8, 2024
• First Posted: October 10, 2024
• Study Start: November 1, 2024
• Primary Completion: November 1, 2025
• Study Completion: November 1, 2025
• Last Updated: October 10, 2024

Record last verified: 2024-09

Data Sharing

• IPD Sharing: Will not share

Locations

TU (2)