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NCT02933060 · ClinicalTrials.gov registry record · Phase 2

Intravenous Fluid Therapy for the Treatment of Emergency Department Patients With Migraine Headache

A Phase 2 study of Migraine Headache, sponsored by The Cooper Health System.

Completed
Registry status
Phase 2
Development phase
50
Enrollment target
1
Study location

NCT02933060: Completed Phase 2 study of Migraine Headache, sponsored by The Cooper Health System.

NCT02933060 is a Phase 2 study of Migraine Headache that has completed, run by The Cooper Health System. The registered enrollment target is 50 participants, below the 151-participant average among 6 other Migraine Headache trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02933060, a Phase 2 study of Migraine Headache, has completed, sponsored by The Cooper Health System.

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

Study Summary

The purpose of this study is to determine whether patients in the emergency department with migraine headache who are administered an intravenous fluid bolus will report greater improvement in pain scores than control patients.

Primary Outcome

The primary outcome will be the difference in verbal pain rating (0 = no pain, 10 = maximum pain) between the start of the study intervention and one hour later, at completion of the intervention. The minimum clinically significant difference between treatment groups on the 0-10 verbal scale is 1.3.

Conditions Studied

Interventions

  • OTHER Control
  • OTHER Normal saline (1000 mL)

Study Locations (1)

New Jersey

  • Cooper Univeristy Hospital - Camden

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2017-01
Est. Completion 2017-09-28
Phase Phase 2
The Cooper Health System

39 total trials

What the finished NCT02933060 record still lists

NCT02933060 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 151-participant average among 6 other Migraine Headache trials with a reported enrollment target (67% lower).

The record links to 1 condition, with Migraine Headache appearing as the primary indexed condition, and to 2 interventions - of which Control is the first listed.

NCT02933060 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT02933060 about?

NCT02933060 is a clinical study titled "Intravenous Fluid Therapy for the Treatment of Emergency Department Patients With Migraine Headache". The purpose of this study is to determine whether patients in the emergency department with migraine headache who are administered an intravenous fluid bolus will report greater improvement in pain scores than control patients.

What is the current status of trial NCT02933060?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2017-01. Estimated completion is 2017-09-28.

What conditions does trial NCT02933060 study?

This clinical trial studies the following conditions: Migraine Headache.

What interventions are being tested in trial NCT02933060?

The interventions under investigation include: Control (OTHER), Normal saline (1000 mL) (OTHER).

Who is sponsoring clinical trial NCT02933060?

This trial is sponsored by The Cooper Health System, which has 39 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02933060 being conducted?

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

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Source: ClinicalTrials.gov NCT02933060, the US trial registry maintained by the National Library of Medicine. NCT02933060 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.