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COMPLETED NA

Preoperative Prevalence of Ulnar Neuropathy and Changes in Ulnar Nerve Latency During Surgery

NCT02533024 · View on ClinicalTrials.gov ↗

Study Summary

This study is to investigate the incidence of undiagnosed ulnar neuropathy in patients undergoing surgery. The investigators hope to determine if patients with ulnar neuropathy have changes in nerve conduction latency during surgery.

Conditions Studied

Interventions

  • OTHER Electromyography

Study Locations (1)

Ohio

  • University of Toledo — Toledo

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2015-08
Est. Completion 2017-04-28
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02533024

The ClinicalTrials.gov registry entry for NCT02533024 describes a study currently listed as completed. It is categorized as NA, 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 4 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Toledo Health Science Campus, which has 5 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 Ulnar Neuropathy appearing as the primary indexed condition, and to 1 intervention — of which Electromyography 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: NCT02533024 reports 1 study location spanning 1 distinct geographic area — top geographies include Ohio. 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 NCT02533024 about?

NCT02533024 is a clinical study titled "Preoperative Prevalence of Ulnar Neuropathy and Changes in Ulnar Nerve Latency During Surgery". This study is to investigate the incidence of undiagnosed ulnar neuropathy in patients undergoing surgery. The investigators hope to determine if patients with ulnar neuropathy have changes in nerve conduction latency during surgery.

What is the current status of trial NCT02533024?

This trial is currently completed. It is a NA study. The enrollment target is 4 participants. The study started on 2015-08. Estimated completion is 2017-04-28.

What conditions does trial NCT02533024 study?

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

What interventions are being tested in trial NCT02533024?

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

Who is sponsoring clinical trial NCT02533024?

This trial is sponsored by University of Toledo Health Science Campus, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02533024 being conducted?

This trial has 1 study location across Ohio. 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