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NCT04702555 · ClinicalTrials.gov registry record

Analgesic Efficacy of Orally Administered VTS-K for Pain Management

A clinical trial, sponsored by Antonios Likourezos.

Completed
Registry status
25
Enrollment target

NCT04702555: Completed study, sponsored by Antonios Likourezos.

NCT04702555 is a clinical trial that has completed, run by Antonios Likourezos. The registered enrollment target is 25 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04702555 has completed, sponsored by Antonios Likourezos.

COMPLETED
Registry status
25 participants
Enrollment target

Study Summary

A combination of ketamine and aspirin for the treatment of acute MSK pain in the ED would confer multimodal analgesia, with the contributions of aspirin and ketamine to an opioid sparing effect. Research on this multimodal approach is sparse, but the minimal empirical evidence supports a clinical benefit to patients in a post orthopedic surgery setting, both in short term and long term. Vitalis Pharmaceuticals (New York, NY) has developed a proprietary formulation of aspirin, VTS-Aspirin, that may deliver faster and stronger pain reduction than traditional aspirin. Preliminary research indicates that combinations of VTS-Aspirin with analgesics may confer greater benefit in pain management than some current standards of care (26). An oral combination drug of VTS-Aspirin and ketamine (VTS-K) would facilitate the shift from IV opioids to a non-IV therapy for patients presenting to the ED with acute MSK pain. This formulation has a potential to provide effective analgesia in the ED with reduced side effects. VTS-K's proprietary oral formulation of established, safe, and well-understood APIs, makes it uniquely appropriate for use in the ED. VTS-K is administered orally, which is suitable for resource-poor environments in which the healthcare setting may be inadequate as well as suitable to improve the throughput of ED Patients by reducing their length of stay. This is especially pertinent given the alternative of IV opioids for pain management of acute MSK pain, which requires both clinical monitoring and equipment, whereas VTS-K promotes weaning off opioids, alleviating the resource consumption.

Primary Outcome

To assess whether VTS-K is effective in reducing acute MSK pain in ED patients using a 11 Point Likert Scale with 0 being no pain, 5 being moderate pain, and 10 being severe pain.

Interventions

  • DRUG VTS-K

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2021-01-08
Est. Completion 2021-12-31
Antonios Likourezos

33 total trials

What the finished NCT04702555 record still lists

NCT04702555 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 25 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which VTS-K is the first listed.

NCT04702555 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04702555 about?

NCT04702555 is a clinical study titled "Analgesic Efficacy of Orally Administered VTS-K for Pain Management". A combination of ketamine and aspirin for the treatment of acute MSK pain in the ED would confer multimodal analgesia, with the contributions of aspirin and ketamine to an opioid sparing effect. Research on this multimodal approach is sparse, but the minimal empirical evidence supports a clinical be...

What is the current status of trial NCT04702555?

This trial is currently completed. The enrollment target is 25 participants. The study started on 2021-01-08. Estimated completion is 2021-12-31.

What interventions are being tested in trial NCT04702555?

The interventions under investigation include: VTS-K (DRUG).

Who is sponsoring clinical trial NCT04702555?

This trial is sponsored by Antonios Likourezos, which has 33 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT04702555, the US trial registry maintained by the National Library of Medicine. NCT04702555 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.