Na-Phenylbutyrate VAscular Trial
Starting soon · Early Phase 1 · Has a placebo group
Conditions studied: Diabetes
In brief
This study will investigate if the drug sodium phenylbutyrate (NaPB) impacts blood pressure and vascular function in healthy volunteers and in patients with diabetes.
Key facts
- Study ID
- NCT06645769
- Run by
- University of Pennsylvania
- People needed
- 30
- Starts
- 2027-06-01
- Expected to finish
- 2029-06-01
- Last updated by the study team
- 2026-07-28
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Over 18 years of age and less than 60.
- Healthy subjects will have no history of diabetes or prediabetes.
- Diabetes subjects can be either insulin dependent or not.
- Able to provide written consent and to comply with the procedures of the study protocol.
You may not qualify if…
- Age <18 or >60
- Pregnant or lactating women.
- Subjects with hypertension or taking any vasodilatory medications, any steroidal drugs, haloperidol, or valproic acid.
- Patients with congestive heart failure, severe renal insufficiency, hepatic failure, or known sodium retention with oedema.
- Active alcohol or substance abuse.
- Use of tobacco within the previous six months.
- Unble to provide written consent and to comply with the procedures of the study protocol.
Full record on ClinicalTrials.gov
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