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Clinical Significance of Sphingosine-1-Phosphate in the Evaluation of Endothelial Function and Cardiovascular Risk in Hypertension

Clinical Significance of Sphingosine-1-Phosphate in the Evaluation of Endothelial Function and Cardiovascular Risk in Hypertension - SEE-THRU BP

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004497
Enrollment
30
Registered
2011-03-10
Start date
2011-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential hypertension

Interventions

SEE-THRU BP is a 16-week, cross-over, prospective, randomized, open, blinded-endpoint (PROBE) study. After a screening phase for eligibility, baseline data are obtained. Then, patients are assigned to
Group 1) or atenolol (50mg, daily
Group 2) for 8 weeks. Group 1: Antihypertensive drugs other than telmisartan, if any at baseline, are continued and not changed throughout the study period. After 8 weeks, telmisartan is switched
Group 2) for 8 weeks. Group 2: Antihypertensive drugs other than atenolol, if any at baseline, are continued and not changed throughout the study period. After 8 weeks, atenolol is switched to t

Sponsors

Nagoya City University Graduate School of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with hypertension who have not been treated with antihypertensive drug

Exclusion criteria

Exclusion criteria: Exclusion criteria are: history of coronary heart disease, heart failure, or stroke; diabetes mellitus; metabolic syndrome; malignant neoplasm; active inflammatory disease; pregnant women

Design outcomes

Primary

MeasureTime frame
Primary endpoint is the change in the plasma S1P concentration and endothelial function from baseline to 8 weeks after each treatment.

Secondary

MeasureTime frame
Secondary endpoints: (1) The change in lipid profiles (total cholesterol, HDL-cholesterol, LDL-cholesterol, triglycerides) from baseline to 8 weeks after each treatment. (2) The change in fasting plasma glucose, C-reactive protein, serotonin, malondialdehyde-modified low-density lipoproteitn (MDA-LDL) from baseline to 8 weeks after each treatment. (3) The change in urine albumin excretion from baseline to 8 weeks after each treatment. (4) The change in brachial-ankle pulse wave velocity from baseline to 8 weeks after each treatment. (5) The change in the number of progenitor cell (CD34+ cell) from baseline to 8 weeks after each treatment. (6) The change in the number of endothelial progenitor cells (positive for DiI-acLDLuptake and FITC-lectin binding staining) from baseline to 8 weeks after each treatment. (7) The change in brachial blood pressure, estimated central aortic pressure, and heart rate from baseline to 8 weeks after each treatment. (8) The change in expression of microRNA associated with endothelial function from baseline to 8 weeks after each treatment.

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026