Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 2

Regulating Blood Pressure During Recovery From Intracerebral Hemorrhage and Ischemic Stroke

NCT04760717 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this research study is to determine whether blood pressure treatment regimens with spironolactone are better than blood pressure treatment regimens without spironolactone at lowering blood pressure in stroke survivors.

Interventions

  • DRUG Spironolactone Pill

Study Locations (5)

Pennsylvania

  • Hospital of the University of Pennsylvania — Philadelphia
  • Temple University Hospital — Philadelphia

Connecticut

  • Yale New Haven Hospital — New Haven

North Carolina

  • Wake Forest Baptist Health — Winston-Salem

Texas

  • University of Texas Health Science Center at Houston — Houston

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2021-03-19
Est. Completion 2025-12
Phase Phase 2

Sponsor

Yale University

1,283 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04760717

The ClinicalTrials.gov registry entry for NCT04760717 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,283 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Ischemic Stroke appearing as the primary indexed condition, and to 1 intervention — of which Spironolactone Pill is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04760717 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Pennsylvania, Connecticut, North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04760717 about?

NCT04760717 is a clinical study titled "Regulating Blood Pressure During Recovery From Intracerebral Hemorrhage and Ischemic Stroke". The purpose of this research study is to determine whether blood pressure treatment regimens with spironolactone are better than blood pressure treatment regimens without spironolactone at lowering blood pressure in stroke survivors.

What is the current status of trial NCT04760717?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 200 participants. The study started on 2021-03-19. Estimated completion is 2025-12.

What conditions does trial NCT04760717 study?

This clinical trial studies the following conditions: Ischemic Stroke, Intracerebral Hemorrhage, Spironolactone. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04760717?

The interventions under investigation include: Spironolactone Pill (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04760717?

This trial is sponsored by Yale University, which has 1,283 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04760717 being conducted?

This trial has 5 study locations across Connecticut, North Carolina, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial