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COMPLETED Phase 4

Isopropyl Alcohol vs Ondansetron for Nausea in the Emergency Department

NCT02760069 · View on ClinicalTrials.gov ↗

Study Summary

This study will compare the efficacy of isopropyl alcohol and conventional anti-emetics with three study arms: (1) inhaled isopropyl alcohol plus oral ondansetron; (2) inhaled isopropyl alcohol plus oral placebo; (3) inhaled placebo plus oral ondansetron.

Conditions Studied

Interventions

  • DRUG Inhaled isopropyl alcohol
  • DRUG Oral ondansetron
  • DRUG Inhaled normal saline
  • DRUG Oral placebo

Study Locations (1)

Texas

  • San Antonio Military Medical Center — San Antonio

Trial Details

FieldValue
Enrollment Target 122 participants
Start Date 2016-01
Est. Completion 2017-11
Phase Phase 4

Sponsor

Brooke Army Medical Center

18 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02760069

The ClinicalTrials.gov registry entry for NCT02760069 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 122 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Brooke Army Medical Center, which has 18 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 Nausea appearing as the primary indexed condition, and to 4 interventions — of which Inhaled isopropyl alcohol 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: NCT02760069 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. 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 NCT02760069 about?

NCT02760069 is a clinical study titled "Isopropyl Alcohol vs Ondansetron for Nausea in the Emergency Department". This study will compare the efficacy of isopropyl alcohol and conventional anti-emetics with three study arms: (1) inhaled isopropyl alcohol plus oral ondansetron; (2) inhaled isopropyl alcohol plus oral placebo; (3) inhaled placebo plus oral ondansetron.

What is the current status of trial NCT02760069?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 122 participants. The study started on 2016-01. Estimated completion is 2017-11.

What conditions does trial NCT02760069 study?

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

What interventions are being tested in trial NCT02760069?

The interventions under investigation include: Inhaled isopropyl alcohol (DRUG), Oral ondansetron (DRUG), Inhaled normal saline (DRUG), Oral placebo (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02760069?

This trial is sponsored by Brooke Army Medical Center, which has 18 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02760069 being conducted?

This trial has 1 study location across Texas. 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