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Efficacy and Safety of Snail Slime and Natural Extracts for Healing in Diabetic Foot Ulcers

Diabetic Foot Ulcer Clinical Trial

Official title:
Clinical Trial Phase I-II of Efficacy and Safety of Snail Slime and Natural Extracts for Healing in Diabetic Foot Ulcers

Clinical Trial Summary

The primary objective is to evaluate the efficacy and safety of the use of a formulation of snail slime and natural extracts, for the curative treatment of ulcer wonds in diabetic foot.

The secondary objetives:

1. To evaluate the efficacy of the use of a formulation of snail slime Helix aspersa Müller and natural extracts (MU001) for the curative treatment of ulcer wonds in diabetic foot with respect to the standard of care, by means the application of patchs that containing the formulation in a treatment period of until 60 days.

2. To determine the safety of the use of a formulation of snail slime Helix aspersa Müller and natural extracts (MU001) in diabetic individuals in a treatment period of until 60 days.

Clinical Trial Description

Clinical Study of phase I-II, controlled, simple blind (in relation with biostatistical analysis), randomized, of formulation that containing snail slime Helix aspersa Müller (Cryptophalus aspersus), natural calendula extract, propolis and excipients (MU001).

The formulation in study MU001 wil be added to the standard of care for healing in diabetic foot indicated. The period of recruitment estimated will be 4 month and the follow-up of the patients will be of until 60 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03166423
Study type Interventional
Source University of Chile
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date November 12, 2015
Completion date July 1, 2017
View Details
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