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ACTIVE NOT RECRUITING

Predicting Concussion Outcomes With Salivary miRNA

NCT02901821 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to identify changes in salivary ribosomal nucleic acid (RNA) expression that are predictive of symptom duration and character following mild traumatic brain injury (mTBI) in children.

Conditions Studied

Interventions

  • GENETIC salivary RNA collection

Study Locations (1)

Pennsylvania

  • Penn State Milton S. Hershey Medical Center — Hershey

Trial Details

FieldValue
Enrollment Target 700 participants
Start Date 2016-01
Est. Completion 2026-06

Sponsor

Milton S. Hershey Medical Center

277 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02901821

The ClinicalTrials.gov registry entry for NCT02901821 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 700 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Milton S. Hershey Medical Center, which has 277 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 Concussion, Mild appearing as the primary indexed condition, and to 1 intervention — of which salivary RNA collection 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: NCT02901821 reports 1 study location spanning 1 distinct geographic area — top geographies include Pennsylvania. 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 NCT02901821 about?

NCT02901821 is a clinical study titled "Predicting Concussion Outcomes With Salivary miRNA". The purpose of this study is to identify changes in salivary ribosomal nucleic acid (RNA) expression that are predictive of symptom duration and character following mild traumatic brain injury (mTBI) in children.

What is the current status of trial NCT02901821?

This trial is currently active not recruiting. The enrollment target is 700 participants. The study started on 2016-01. Estimated completion is 2026-06.

What conditions does trial NCT02901821 study?

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

What interventions are being tested in trial NCT02901821?

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

Who is sponsoring clinical trial NCT02901821?

This trial is sponsored by Milton S. Hershey Medical Center, which has 277 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02901821 being conducted?

This trial has 1 study location across Pennsylvania. 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