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NCT05489601
Non-intrusive Detection of Temporary Neurologic Impairment by Opioids
trial testing Oxycodone in Neurologic Impairment by Opioids in 17 participants. Completed in 29 March 2022.
29 March 2022
Quick facts
| Lead sponsor | Zxerex Corporation |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 17 |
| Start date | 28 February 2020 |
| Primary completion | 29 March 2022 |
| Estimated completion | 29 March 2022 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Oxycodone (oxycodone) — full drug profile →
Conditions studied
- Neurologic Impairment by Opioids — all drugs for Neurologic Impairment by Opioids →
Sponsor
Zxerex Corporation
Who can join
Adults 21 to 59, any sex, with Neurologic Impairment by Opioids. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The investigators aim to prove the feasibility of a non-invasive means to identify temporary neurological impairment resulting from the use of a commonly prescribed opioid by identifying an oculomotor biosignature associated with temporary neurologic impairment in pain-free opioid-naïve subjects, and to initiate the development of such a signature. The investigators also sought to establish the presence of a dose-dependent biosignature for opioid impairment.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT05489601
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Oxycodone
Trials testing the same drug.
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- NCT06757140 — Opioid Drug Interaction Study · Phase 1, PHASE2 · recruiting
- NCT05965492 — Multimodal Pain Package vs. Regular Formulation for Pain Management in Ambulatory Spinal Surgery · Phase 3 · withdrawn
- NCT06517069 — Effect of TEAS Combined With Oxycodone on Postoperative Visceral Pain in Gynecologic Laparoscopic Patients · NA · recruiting
- NCT06340932 — Impact of Opioid Avoidance Protocol for ACL Reconstruction · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05489601 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Zxerex Corporation
- Last refreshed: 5 August 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05489601.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing