- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07760623
Common Carotid Artery-Renal Artery-Femoral Artery Survey for Hypertension (CRF Survey)
Common Carotid Artery-Renal Artery-Femoral Artery Survey for Hypertension (CRF Survey)
Study Overview
Status
Intervention / Treatment
Detailed Description
The study of the first degree, both sides in some of the aortic branch group, the effect and/or cause of systemic arterial hypertension compared to normotension. According to the theory of systemic arterial hypertension, the arterial resistance and high blood volume flow causing systemic arterial hypertension, the cause of arterial resistance and high blood volume flow evaluation may trace back to the possible actual cause of systemic arterial hypertension by backward investigation. Despite the fact that target organ damage is the crucial maneuver of hypertension evaluation, both sides of the common carotid artery, renal artery, and femoral artery may cause systemic arterial hypertension and may imply that feasible to predict the end organ of stroke, ESRD, and amputated-type arterial occlusion, respectively.
This study belongs to 2 questions
- Can the main aortic branch be evidence of a cause of systemic arterial hypertension following high resistance and/or high fluid flow by theory?
- Can the main aortic branch be a marker of evidence of endpoint organ damage?
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Nathaphong Dejthida, Medical Degree
- Phone Number: +66819220662
- Email: bnnatto@gmail.com
Study Locations
-
-
Bangkok
-
Vadhana, Bangkok, Thailand, 10110
- Invstigation center
-
Contact:
- Nathaphong Dejthida, Medical Degree
- Phone Number: 0819220662
- Email: bnnatto@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults ≥18 years with diagnosed hypertension by a clinician, both untreated and treated, including successfully treated participants.
Imaging evidence of at least 1 list of
- Common carotid artery
- Renal artery
- Femoral artery
Exclusion Criteria:
- Fatal pathology and imaging
- Pediatric or pregnant participants
- Small vessel angiogram
- Intravascular endoscopy
- Intra-operative estimation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Common Carotid Artery
The group of hypertensive patients were underwent in angiographic imaging such as ultrasonography, CR/MR, real-time intravascular contrast media angiography of any side of Common Carotid Artery.
|
Radiographic diameter in cm. of each side of one of Common Carotid Artery, Renal Artery and Femoral Artery
Any kind of radiographic measurement of Peak Systolic Velocity and/or End Diastolic Velocity (cm/s)
|
|
Renal Artery
The group of hypertensive patients were underwent in angiographic imaging such as ultrasonography, CR/MR, real-time intravascular contrast media angiography of any side of Renal Artery.
|
Radiographic diameter in cm. of each side of one of Common Carotid Artery, Renal Artery and Femoral Artery
Any kind of radiographic measurement of Peak Systolic Velocity and/or End Diastolic Velocity (cm/s)
|
|
Femoral Artery
The group of hypertensive patients were underwent in angiographic imaging such as ultrasonography, CR/MR, real-time intravascular contrast media angiography of any side of Femoral Artery.
|
Radiographic diameter in cm. of each side of one of Common Carotid Artery, Renal Artery and Femoral Artery
Any kind of radiographic measurement of Peak Systolic Velocity and/or End Diastolic Velocity (cm/s)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Median of diameter of common carotid artery, renal artery and femoral artery in hypertension patients.
Time Frame: 1 years
|
Radiographic measurement includes ultrasonography, CT/MR imaging, and intravascular contrast media imaging that measure the diameter in cm. unit of any side of common carotid artery and/or renal artery and/or femoral artery in hypertension patients.
|
1 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Common Carotid Artery Function
Time Frame: 1 year
|
Any kind of radiographic measurement one of Peak Systolic Velocity (cm/s) or End Diastolic Velocity (cm/s) of any side of Common Carotid Artery
|
1 year
|
|
Renal Artery Function
Time Frame: 1 year
|
Any kind of radiographic measurement one of Peak Systolic Velocity (cm/s) or End Diastolic Velocity (cm/s) of any side of Renal Artery
|
1 year
|
|
Femoral Artery Function
Time Frame: 1 year
|
Any kind of radiographic measurement one of Peak Systolic Velocity (cm/s) or End Diastolic Velocity (cm/s) of any side of Femoral Artery
|
1 year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
All-cause mortality outcomes
Time Frame: 1 year
|
Incidence of mortality rate (case per 1,000 person-year) of hypertensive participants were underwent measurement the diameter one side of one of common carotid artery and/or renal artery and/or femoral artery
|
1 year
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NathaphongD
- PROSPERO (Other Identifier: CRD420261464383)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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