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COMPLETED Phase 2

Activated Vitamin D for the Prevention and Treatment of Acute Kidney Injury

NCT02962102 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to assess the efficacy of calcifediol (25-hydroxyvitamin D) and calcitriol (1,25-dihydroxyvitamin D) in preventing and reducing the severity of acute kidney injury (AKI) in critically ill patients.

Interventions

  • DRUG Placebos
  • DRUG Calcitriol
  • DRUG Calcifediol

Study Locations (1)

Massachusetts

  • Brigham and Women's Hospital — Boston

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2017-04-03
Est. Completion 2020-08-06
Phase Phase 2

Sponsor

David Leaf

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02962102

The ClinicalTrials.gov registry entry for NCT02962102 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 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is David Leaf, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Acute Kidney Injury appearing as the primary indexed condition, and to 3 interventions — of which Placebos 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: NCT02962102 reports 1 study location spanning 1 distinct geographic area — top geographies include Massachusetts. 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 NCT02962102 about?

NCT02962102 is a clinical study titled "Activated Vitamin D for the Prevention and Treatment of Acute Kidney Injury". The purpose of this study is to assess the efficacy of calcifediol (25-hydroxyvitamin D) and calcitriol (1,25-dihydroxyvitamin D) in preventing and reducing the severity of acute kidney injury (AKI) in critically ill patients.

What is the current status of trial NCT02962102?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 150 participants. The study started on 2017-04-03. Estimated completion is 2020-08-06.

What conditions does trial NCT02962102 study?

This clinical trial studies the following conditions: Acute Kidney Injury, Critically Ill. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02962102?

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

Who is sponsoring clinical trial NCT02962102?

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

Where is trial NCT02962102 being conducted?

This trial has 1 study location across Massachusetts. 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