MR Antagonist and LSD1
Running, not enrolling · Phase 4
Conditions studied: Hypertension, Mineralocorticoid Excess
In brief
Lysine specific demethylase-1 (LSD1) is an epigenetic regulator of gene transcription involved in the pathophysiology of elevated blood pressure and likely renal damage in Blacks. This project investigates whether a genetically driven anti-hypertensive approach proves superior in controlling blood pressure and mitigating renal injury in Blacks who carry the risk allele for LSD1 (rs587168). The findings of these investigations may lead to a new approach in treating a subset (\~30%) of the essential hypertension population (Black LSD1 risk allele hypertensives).
Key facts
- Study ID
- NCT04840342
- Run by
- Brigham and Women's Hospital
- People needed
- 300
- Starts
- 2022-02-03
- Expected to finish
- 2026-06-01
- Last updated by the study team
- 2026-04-29
Who can join
Age: 17 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- untreated as well as currently treated hypertensives
- rs587168 allele carriers
- not on more than two anti-hypertensives
- normal renal, metabolic, electrolyte, and CBC laboratory tests
- self-identified Black race
- age >17 yrs.
You may not qualify if…
- known cardiac disease other than HTN
- renal, circulatory or neurologic diseases
- diabetes
- smoking
- secondary HTN as indicated by history, physical examination or screening blood and urine tests
- smoking
- any drug therapy, except for anti-hypertensives and stable thyroid medication replacement
Where it is running
- Brigham and Women's — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.