Last reviewed · How we verify
NCT06409949
MitoQ Treatment of Claudication: Myofiber and Micro-vessel Pathology
NA trial testing Walking assessment in Peripheral Arterial Disease in 60 participants. Currently enrolling.
1 October 2026
Quick facts
| Lead sponsor | University of Nebraska |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 June 2023 |
| Primary completion | 1 October 2026 |
| Estimated completion | 1 June 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Walking assessment
- QOL Survey
- Ankle pressure at rest and after stress
- Muscle Oxygen
- Serum MitoQ Level
- Needle Biopsy
Conditions studied
- Peripheral Arterial Disease — all drugs for Peripheral Arterial Disease →
Sponsor
University of Nebraska
Who can join
21 and older, any sex, with Peripheral Arterial Disease. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Walking Impairment: maximum treadmill distance
Time frame: Before and After 6 months of treatment with MitoQ or placebo
Evaluation of maximum walking distance on treadmill until participant chooses to stop due to pain in his legs.
Sponsor's own description
In our research, we are delving into whether taking MitoQ for six months can improve the symptoms and function of people diagnosed with peripheral artery disease, especially those who suffer from leg pain while walking, known as intermittent claudication. We will be checking if MitoQ helps people with claudication walk better, be more active every day, feel better about their lives, and if it enhances the health of their leg muscles.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Mitochondria-targeted nanotechnology in cardiovascular diseases: a review of recent advances.
Sun S, Wu M, Zhang P, Sun L, et al · · 2026 · PMID 42022751 · DOI 10.1093/rb/rbag040
Verify or expand the search:
- PubMed search for NCT06409949
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other University of Nebraska trials
Trials by the same sponsor.
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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 NCT06409949 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Nebraska
- Last refreshed: 21 February 2026
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/NCT06409949.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing