Delivery of Yamani-15/5 Chemical Solution for PAD

Status Withdrawn

Clinical Trial Summary

This is a feasibility pilot study to evaluate the impact of local delivery of Yamani-15/5 (combination of L-Lactic acid 15% and D-Gluconic acid 5%) on vascular calcification of lower extremities in patients with severe peripheral arterial disease (PAD) who were deemed to have unreconstructable arterial disease and who have already been scheduled to undergo limb amputation (below knee or above knee amputation).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02539303
Study type	Interventional
Source	Mayo Clinic
Contact
Status	Withdrawn
Phase	Phase 1
Start date	August 2015
Completion date	August 2023

View Details

See also
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