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COMPLETED Phase 4

Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen

NCT01334944 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to determine the safety of a single dose of intravenous ibuprofen administered over 5-10 minutes for the treatment of fever or pain in the hospital setting.

Conditions Studied

Interventions

  • DRUG Intravenous ibuprofen

Study Locations (13)

North Carolina

  • The University of North Carolina Hospitals — Chapel Hill
  • Duke University Medical Center — Durham
  • The Moses H. Cone Memorial Hospital — Greensboro
  • Wake Forest University Baptist Medical Center — Winston-Salem

Ohio

  • Fairview — Cleveland
  • The Ohio State University Medical Center — Columbus

California

  • UCSD — San Diego

Connecticut

  • Danbury — Danbury

Florida

  • University of Miami - Miller School of Medicine — Miami

Georgia

  • Grady — Atlanta

Massachusetts

  • Beth Israel Deaconnes MC — Boston

New York

  • Columbia — New York

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2011-06
Est. Completion 2012-10
Phase Phase 4

Sponsor

Cumberland Pharmaceuticals

12 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01334944

The ClinicalTrials.gov registry entry for NCT01334944 describes a study currently listed as completed. It is categorized as Phase 4, 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 Cumberland Pharmaceuticals, which has 12 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 Pain appearing as the primary indexed condition, and to 1 intervention — of which Intravenous ibuprofen 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: NCT01334944 reports 13 study locations spanning 9 distinct geographic areas — top geographies include North Carolina, Ohio, California. 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 NCT01334944 about?

NCT01334944 is a clinical study titled "Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen". The primary objective of this study is to determine the safety of a single dose of intravenous ibuprofen administered over 5-10 minutes for the treatment of fever or pain in the hospital setting.

What is the current status of trial NCT01334944?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 150 participants. The study started on 2011-06. Estimated completion is 2012-10.

What conditions does trial NCT01334944 study?

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

What interventions are being tested in trial NCT01334944?

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

Who is sponsoring clinical trial NCT01334944?

This trial is sponsored by Cumberland Pharmaceuticals, which has 12 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01334944 being conducted?

This trial has 13 study locations across California, Connecticut, Florida, Georgia, 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