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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05135130
Other study ID # ON101CLOS01
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 4, 2021
Est. completion date January 2022

Study information

Verified date November 2021
Source Oneness Biotech Co., Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to evaluate the medical cost of illness for DFUs on the patients who had used ON101 or Aquacel® in the ON101CLCT02 trial.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 176
Est. completion date January 2022
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 79 Years
Eligibility No additional inclusion or exclusion criteria will be applied.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
ON101 Cream
Not applicable in this retrospective study

Locations

Country Name City State
Taiwan China Medical University Hospital Taichung City

Sponsors (1)

Lead Sponsor Collaborator
Oneness Biotech Co., Ltd.

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Demographic characteristics Up to two years after the patient had completed or early withdrawn from the ON101CLCT02 trial
Primary Wound characteristics of DFUs (classification and proportion) Up to two years after the patient had completed or early withdrawn from the ON101CLCT02 trial
Primary Proportion of DFU recurrence after completing or withdrawing from the ON101CLCT02 trial Up to two years after the patient had completed or early withdrawn from the ON101CLCT02 trial
Primary Medical costs due to DFUs Up to two years after the patient had completed or early withdrawn from the ON101CLCT02 trial
Primary Proportion of wound infection, gangrene, and amputation Up to two years after the patient had completed or early withdrawn from the ON101CLCT02 trial
Primary Frequency of wound infection, gangrene, and amputation Up to two years after the patient had completed or early withdrawn from the ON101CLCT02 trial
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