Targeting endoplasmic reticulum stress to treat hypertension
Official title: Targeting Endoplasmic Reticulum Stress in Human Hypertension
Run by University of North Texas Health Science Center · NCT06025630 · Data updated 2026-11-12
This study is testing if a medication called TUDCA can help people with controlled high blood pressure by reducing stress in their cells.
Quick facts
| Phase | Phase1; Phase2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 70 (estimated) |
| Sponsor | University of North Texas Health Science Center Academic / other |
| Locations | 1 site (Fort Worth, Texas) |
| Status | Recruiting |
| Started | August 15, 2023 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | March 28, 2025 |
| Trial ID | NCT06025630 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 to 80 with controlled hypertension and a body mass index under 35.
✕Probably not a fit
Patients with uncontrolled hypertension or those with a body mass index over 35 may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the role of endoplasmic reticulum stress in human hypertension by administering tauroursodeoxycholic acid (TUDCA) to participants. It is a single-blind, placebo-controlled trial designed to assess whether inhibiting endoplasmic reticulum stress can improve blood pressure regulation. The study will involve participants aged 18 to 80 with controlled hypertension, who will receive either TUDCA or a placebo over a specified period. The trial aims to fill a gap in understanding how endoplasmic reticulum stress affects hypertension in humans, building on previous animal model findings.
Why it matters
Potential benefit: If successful, this approach could provide a novel treatment option for managing hypertension in patients.
How similar studies have gone: While there is strong evidence from animal models regarding the role of endoplasmic reticulum stress in hypertension, this approach has not been previously tested in humans.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. 18 to 80 years of age 2. No tobacco/nicotine use within preceding 6 months (e.g., cigarettes, chewing tobacco, nicotine gum or patches) 3. Systolic blood pressure \<140 mmHg; diastolic blood pressure \<90 mmHg (obtained at the Screening and Familiarization Visit) 4. Normal 12-lead ECG (obtained at the Screening and Familiarization Visit and reviewed by a board-certified physician) 5. 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) 6. Body mass index (BMI) \<35 unless athletic/muscular build; calculation = body weight (kg)/height (m2); 7. Females only: documentation of a negative pregnancy test prior to the familiarization and experimental sessions unless post-menopausal Exclusion Criteria: 1. Not meeting the defined age criteria 2. Body mass index (BMI) \>35 unless athletic/muscular build; calculation = body weight (kg)/height (m2) 3. Any tobacco/nicotine use within the last 6 months (e.g., cigarettes, chewing tobacco, nicotine gum or patches) 4. Positive pregnancy test 5. Females with an erratic/irregular menstrual cycle 6. Females who are breastfeeding 7. 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) 8. Subjects who weigh less than 80 lbs. 9. Use of prescription drugs, non-prescription drugs, dietary supplements or herbal medicines known to alter vascular function unless cleared prior to the study 10. Use of beta blockers 11. Daily use of bronchodilators 12. Use of anti-coagulant therapy 13. Implanted medical devices (e.g. cardiac pacemaker) 14. Current or past history of hyperthyroidism, or other thyroid hormone-related disease 15. Current use of hormone replacement therapy (e.g., estrogen, testosterone) 16. HbA1c \>5.6 17. Resting systolic blood pressure of \<100 mmHg; \>140mmHg or diastolic blood pressure \>90mmHg 18. Abnormal 12-lead ECG or uncontrolled heart rhythm issues causing symptoms, or an unstable blood pressure 19. History of cerebrovascular abnormalities (e.g., prior stroke, transient ischemic attacks, epilepsy) 20. Known history of atherosclerosis of the carotid arteries (i.e., plaque formation) 21. History of concussion and or other loss of consciousness within the preceding 30 days 22. Autonomic dysfunction (e.g., Shy-Drager Syndrome, Bradbury-Eggleston syndrome, sinus arrhythmia, idiopathic orthostatic hypotension, fainting disorder) 23. Respiratory illnesses (e.g., chronic asthma (including exercise-induced asthma), Chronic Obstructive Pulmonary Disease, Reactive Airway Disease) 24. Any prior history of anaphylaxis, not just prior reactions to the materials used in this study 25. Severe phobia of needles 26. 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
Where it's running
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University of North Texas Health Science Center
Fort Worth, Texas, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.