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RECRUITING Phase 2

Ketamine in Patients Undergoing TEVAR Procedures Receiving NCI

NCT04600089 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study is to identify the opioid-sparing effects, and pain-reduction potential of low dose, sub-dissociative ketamine on patients undergoing thoracic endovascular aortic repair (TEVAR) procedures receiving naloxone continuous infusion (NCI).

Interventions

  • DRUG Ketamine
  • DRUG Saline

Study Locations (1)

Kentucky

  • University of Kentucky Medical Center — Lexington

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2020-12-08
Est. Completion 2027-08
Phase Phase 2

Sponsor

Sam Tyagi

28 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04600089

The ClinicalTrials.gov registry entry for NCT04600089 describes a study currently listed as recruiting. It is categorized as Phase 2, 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 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sam Tyagi, which has 28 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions — of which Ketamine 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: NCT04600089 reports 1 study location spanning 1 distinct geographic area — top geographies include Kentucky. 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 NCT04600089 about?

NCT04600089 is a clinical study titled "Ketamine in Patients Undergoing TEVAR Procedures Receiving NCI". The objective of this study is to identify the opioid-sparing effects, and pain-reduction potential of low dose, sub-dissociative ketamine on patients undergoing thoracic endovascular aortic repair (TEVAR) procedures receiving naloxone continuous infusion (NCI).

What is the current status of trial NCT04600089?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2020-12-08. Estimated completion is 2027-08.

What conditions does trial NCT04600089 study?

This clinical trial studies the following conditions: Postoperative Pain, Thoracoabdominal Aortic Aneurysm, Descending Aortic Dissection. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04600089?

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

Who is sponsoring clinical trial NCT04600089?

This trial is sponsored by Sam Tyagi, which has 28 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04600089 being conducted?

This trial has 1 study location across Kentucky. 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