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NCT04271241
Vascular Function Improvements After Chronic Passive Stretching
NA trial testing Passive stretching (PS) training in Vasodilation in 39 participants. Completed in 7 February 2020.
7 January 2020
Quick facts
| Lead sponsor | University of Milan |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 39 |
| Start date | 7 January 2019 |
| Primary completion | 7 January 2020 |
| Estimated completion | 7 February 2020 |
| Sites | 1 location across Italy |
Drugs / interventions tested
- Passive stretching (PS) training
Conditions studied
- Vasodilation — all drugs for Vasodilation →
- Vasoconstriction — all drugs for Vasoconstriction →
- Stretch — all drugs for Stretch →
- Sympathetic; Imbalance — all drugs for Sympathetic; Imbalance →
Sponsor
University of Milan
Who can join
18 and older, any sex, with Vasodilation or Vasoconstriction. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Acutely, during different bouts of passive stretching (PS), blood flow (Q ̇) and shear rate ( ) in the feeding artery of the stretched muscles increases during the first two elongations and then it reduces during the following bouts. This hyperemic response during the first two elongations is mediated by the local release of vasoactive molecules (e.g. nitric oxide, NO). This phenomenon disappears during the following elongations due to the NO and other vasoactive molecule depletion. The relaxation phase between stretching bouts, instead, is always characterized by hyperemia as results of stretch-induced peripheral resistances decrease. Whether chronic PS administration may influence vascular function is still a matter of investigation. The hypothesis is that repetitive PS-induced Q ̇ and changes may be an enough stimulus to provoke increments in NO bioavailability, thus improving vasomotor response.
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 NCT04271241
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT04271241 (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 University of Milan
- Last refreshed: 17 February 2020
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/NCT04271241.
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