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COMPLETED Phase 2

Verapamil as Therapy for Children and Young Adults With Dravet Syndrome

NCT01607073 · View on ClinicalTrials.gov ↗

Study Summary

This study will assess how well the drug verapamil can improve control of seizures and dysautonomia symptoms in children and young adults diagnosed with Dravet syndrome. The safety of verapamil when given with all concomitant medications will also be assessed.

Conditions Studied

Interventions

  • DRUG Verapamil

Study Locations (4)

Minnesota

  • Mayo Clinic — Rochester
  • Gillette Children's Specialty Healthcare — Saint Paul

Illinois

  • Children's Memorial Hospital — Chicago

New Hampshire

  • Mary Hitchcock Memorial Hospital — Lebanon

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2012-04
Est. Completion 2015-01
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01607073

The ClinicalTrials.gov registry entry for NCT01607073 describes a study currently listed as completed. 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 2 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gillette Children's Specialty Healthcare, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Dravet Syndrome appearing as the primary indexed condition, and to 1 intervention — of which Verapamil 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: NCT01607073 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Minnesota, Illinois, New Hampshire. 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 NCT01607073 about?

NCT01607073 is a clinical study titled "Verapamil as Therapy for Children and Young Adults With Dravet Syndrome". This study will assess how well the drug verapamil can improve control of seizures and dysautonomia symptoms in children and young adults diagnosed with Dravet syndrome. The safety of verapamil when given with all concomitant medications will also be assessed.

What is the current status of trial NCT01607073?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2012-04. Estimated completion is 2015-01.

What conditions does trial NCT01607073 study?

This clinical trial studies the following conditions: Dravet Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01607073?

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

Who is sponsoring clinical trial NCT01607073?

This trial is sponsored by Gillette Children's Specialty Healthcare, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01607073 being conducted?

This trial has 4 study locations across Illinois, Minnesota, New Hampshire. 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