Efficacy and Safety of AJU-C52 in Essential Hypertension Patients
NCT06416865
Cardiovascular Diseases, Essential Hypertension
Seoul, South Korea
View Trial DetailsNCT Number: NCT01295021
The purpose of this NIS is to assess the prevalence of sympathetic overactivity in patients with newly diagnosed essential hypertension.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Research Site, Agartala, India
MC MD
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Visit 1-3: heart rate & Blood pressure, treatment presribed by physician. The interval between visit 1 and visit 2 is upto 4 weeks and interval between visit 2 & visit 3 is upto 4 weeks depending on Investigators discretion.
Time frame: Visits 1-3
Time frame: 1st visit
Time frame: Visits 1-3
Looking for future studies?
Notify MeAstraZeneca
Industry
A Non Interventional, Cross Sectional, Study on the Prevalence of Sympathetic Overactivity in Hypertensive Patients.
Acronym: SORT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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