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Not yet recruitingNCT07760623CRF SurveyUpdated Nov 3, 2026

Common Carotid Artery-Renal Artery-Femoral Artery Survey for Hypertension

An observational study in Hypertension, Hypertension (HTN) and Artery Disease, sponsored by DejthidaNathaphong. Not yet recruiting at 1 site in Thailand. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by DejthidaNathaphong · Observational

Updated Nov 3, 2026Start date movedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

To evaluate both sides of the common carotid artery, renal artery, and femoral artery in Hypertension patient that cause of systemic arterial hypertension and/or the effects of target organ damage, both structural and functional markers.

Read the 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

  1. Can the main aortic branch be evidence of a cause of systemic arterial hypertension following high resistance and/or high fluid flow by theory?
  2. Can the main aortic branch be a marker of evidence of endpoint organ damage?
02

Conditions studied

  • Hypertension
  • Hypertension (HTN)
  • Artery Disease
  • Target Organ Damage

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Keywords

  • hypertension
  • common carotid artery
  • renal artery
  • femmoral artery
  • vascular resistant
03

In context

Hypertension

6,114 studies on the registry are indexed under Hypertension; 912 are open to participants now.

This study's planned enrollment of 100 is below the median of 350 across 1,163 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

DejthidaNathaphong is the lead sponsor of 4 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Hypertensive patient who underwent the radiographic measurement of structure and function of carotid artery, renal artery or femoral artery

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Fatal pathology and imaging
  • Pediatric or pregnant participants
  • Small vessel angiogram
  • Intravascular endoscopy
  • Intra-operative estimation
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

    Other: Diameter measurement · Other: Velocity

  • 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.

    Other: Diameter measurement · Other: Velocity

  • 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.

    Other: Diameter measurement · Other: Velocity

Interventions

  • OtherDiameter measurement

    Radiographic diameter in cm. of each side of one of Common Carotid Artery, Renal Artery and Femoral Artery

  • OtherVelocity

    Any kind of radiographic measurement of Peak Systolic Velocity and/or End Diastolic Velocity (cm/s)

06

What researchers measure

Primary outcomes

  1. Median of diameter of common carotid artery, renal artery and femoral artery in hypertension patients.

    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.

    Time frame: 1 years

Secondary outcomes

  1. Common Carotid Artery Function

    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

    Time frame: 1 year

  2. Renal Artery Function

    Any kind of radiographic measurement one of Peak Systolic Velocity (cm/s) or End Diastolic Velocity (cm/s) of any side of Renal Artery

    Time frame: 1 year

  3. Femoral Artery Function

    Any kind of radiographic measurement one of Peak Systolic Velocity (cm/s) or End Diastolic Velocity (cm/s) of any side of Femoral Artery

    Time frame: 1 year

Other outcomes

  1. All-cause mortality outcomes

    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

    Time frame: 1 year

07

Study locations

1 site
  • Invstigation center
    Vadhana, Bangkok 10110, Thailand
08

References and documents

Related links

Individual participant data

Plan to share: No

09

Updates

2 registry updates since Sep 25, 2026
Start date
Aug 1, 2026→Nov 15, 2026
moved 2 times, Oct 1, 2026 – Nov 3, 2026
Show all 2 updates
  1. Nov 3, 2026
    Start date Oct 1, 2026→Nov 15, 2026
    + 1 other change: verification date
  2. Oct 1, 2026
    Start date Aug 1, 2026→Oct 1, 2026
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07760623
Lead sponsor
DejthidaNathaphong
Responsible party
Nathaphong Dejthida (Principle Investigator, DejthidaNathaphong) — Principal investigator
First posted
Aug 12, 2026
Start date
Nov 15, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
May 18, 2027 (estimated)
Last update
Nov 3, 2026

Study contacts

Nathaphong Dejthida, Medical Degree
Contact
bnnatto@gmail.com
+66819220662

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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