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NCT02020304 · ClinicalTrials.gov registry record · Phase 2

Combined Spinal-Epidural Temperature and Duration of Action

A Phase 2 study of Pain, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 2
Development phase
58
Enrollment target
1
Study location

NCT02020304 is a Phase 2 study of Pain that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 58 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02020304, a Phase 2 study of Pain, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 2
Development phase
58 participants
Enrollment target
1
Study location

Study Summary

The hypothesis is that a combined spinal-epidural drug at refrigerated temperature will have a shorter period of pain relief than that maintained at room temperature. The temperature of the dose of medication will be measure with an infrared thermometer immediately prior (within 5 minutes) to administration.

Conditions Studied

Pain

Interventions

  • DRUG combined spinal epidural

Study Locations (1)

North Carolina

  • Forsyth Medical Center - Winston-Salem

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2013-08-29
Est. Completion 2014-05-04
Phase Phase 2

Sponsor

Wake Forest University Health Sciences

1,140 total trials

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What the Registry Record Tells You About NCT02020304

The ClinicalTrials.gov registry entry for NCT02020304 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 58 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (81% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 1 intervention - of which combined spinal epidural is the first listed.

NCT02020304 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT02020304 about?

NCT02020304 is a clinical study titled "Combined Spinal-Epidural Temperature and Duration of Action". The hypothesis is that a combined spinal-epidural drug at refrigerated temperature will have a shorter period of pain relief than that maintained at room temperature. The temperature of the dose of medication will be measure with an infrared thermometer immediately prior (within 5 minutes) to admini...

What is the current status of trial NCT02020304?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 58 participants. The study started on 2013-08-29. Estimated completion is 2014-05-04.

What conditions does trial NCT02020304 study?

This clinical trial studies the following conditions: Pain.

What interventions are being tested in trial NCT02020304?

The interventions under investigation include: combined spinal epidural (DRUG).

Who is sponsoring clinical trial NCT02020304?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02020304 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.