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NCT06025630RecruitingPhase 1/2

Targeting Endoplasmic Reticulum Stress in Human Hypertension

Source: ClinicalTrials.gov · Last updated 28 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

There is strong evidence suggesting that endoplasmic reticulum stress contributes to neurogenic and vascular hypertension in various animal models, however this has never been explored in humans. Therefore, this project will fill this gap by performing a single-blind, placebo-controlled trial in humans with hypertension.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
70 (estimated)
First submitted
23 Aug 2023
Start date
15 Aug 2023
Primary completion date
31 Dec 2028
Lead sponsor
University of North Texas Health Science Center
NCT number
NCT06025630

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 70
  • From 15 Aug 2023 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Women who are prescribed a continually releasing hormonal contraceptive (e.g. NuvaRingTM or other hormone releasing vaginal rings, Depo Provera shot, or birth control implants such as Nexplanon)
  • Use of prescription drugs, non-prescription drugs, dietary supplements or herbal medicines known to alter vascular function unless cleared prior to the study
  • Use of anti-coagulant therapy
  • Current use of hormone replacement therapy (e.g., estrogen, testosterone)
  • History of cerebrovascular abnormalities (e.g., prior stroke, transient ischemic attacks, epilepsy)
  • Any prior history of anaphylaxis, not just prior reactions to the materials used in this study

Other illness

  • Implanted medical devices (e.g. cardiac pacemaker)
  • Current or past history of hyperthyroidism, or other thyroid hormone-related disease
  • Abnormal 12-lead ECG or uncontrolled heart rhythm issues causing symptoms, or an unstable blood pressure
  • Known history of atherosclerosis of the carotid arteries (i.e., plaque formation)
  • History of concussion and or other loss of consciousness within the preceding 30 days
  • Autonomic dysfunction (e.g., Shy-Drager Syndrome, Bradbury-Eggleston syndrome, sinus arrhythmia, idiopathic orthostatic hypotension, fainting disorder)
  • Respiratory illnesses (e.g., chronic asthma (including exercise-induced asthma), Chronic Obstructive Pulmonary Disease, Reactive Airway Disease)

Lab values

  • HbA1c \>5.6
  • Latex allergy aa) Known allergies or sensitivities to substances used in the study (e.g., Lidocaine HCL, sodium nitroprusside, acetylcholine, phentolamine, L-NAME, TUDCA, or related drugs) bb) Donated blood within the last 60 days cc) History or family history of abnormal blood clotting, clots in deep veins in the legs or pelvis, or blood clots to the lungs dd) History of alcohol or drug abuse which inhibits the subject's ability to complete this study ee) Individuals who have had mastectomies ff) History of methemoglobinemia gg) Current diagnosis of anemia hh) Current Fever (oral temp \>99.5 °F/ 37.5 °C) ii) Current use of PDE3 inhibitors (e.g., Viagra) or soluble guanylate cyclase (sGC) stimulators (e.g., riociguat), or unwillingness to withhold medication for 2 weeks prior to laboratory testing jj) Current diagnosis of cancer kk) Cardiac surgery or cardiac events (e.g., coronary artery bypass graft surgery, myocardial infarction, heart failure) ll) Diagnosis of neurological disease or cognitive dysfunction

Age

  • Not meeting the defined age criteria

Other

  • Body mass index (BMI) \>35 unless athletic/muscular build; calculation = body weight (kg)/height (m2)
  • Any tobacco/nicotine use within the last 6 months (e.g., cigarettes, chewing tobacco, nicotine gum or patches)
  • Positive pregnancy test
  • Females with an erratic/irregular menstrual cycle
  • Females who are breastfeeding
  • Subjects who weigh less than 80 lbs.
  • Use of beta blockers
  • Daily use of bronchodilators
  • Resting systolic blood pressure of \<100 mmHg; \>140mmHg or diastolic blood pressure \>90mmHg
  • Severe phobia of needles

Who the study is looking for

  • 18 to 80 years of age
  • No tobacco/nicotine use within preceding 6 months (e.g., cigarettes, chewing tobacco, nicotine gum or patches)
  • Systolic blood pressure \<140 mmHg; diastolic blood pressure \<90 mmHg (obtained at the Screening and Familiarization Visit)
  • Normal 12-lead ECG (obtained at the Screening and Familiarization Visit and reviewed by a board-certified physician)
  • Normal clinical results from a medical exam reviewed by a board-certified physician (e.g., General Health Questionnaire obtained at the Screening and Familiarization Visit)
  • Body mass index (BMI) \<35 unless athletic/muscular build; calculation = body weight (kg)/height (m2);
  • Females only: documentation of a negative pregnancy test prior to the familiarization and experimental sessions unless post-menopausal

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of North Texas Health Science Center
Coordinator of this site? Confirm its status
Fort WorthUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.