NCT05183698

Brief Summary

Evaluation and characterization of autofluorescence signals of tissue in and around wounds as identified by MolecuLight fluorescence image.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
11

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Feb 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 7, 2021

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 11, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

February 24, 2022

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2022

Completed
Last Updated

June 25, 2026

Status Verified

June 1, 2026

Enrollment Period

9 months

First QC Date

December 7, 2021

Last Update Submit

June 23, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Spectra of autofluorescent signatures of tissue in and around the wounds

    Spectral characterization (i.e. emission curve including intensity) of the autofluorescence signal from wound tissue and surrounding tissue will be catalogued from all 50 study participants.

    2 months

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with chronic and/or acute wound

You may qualify if:

  • Patients presenting with acute or chronic wounds
  • years or older
  • Willing to consent

You may not qualify if:

  • Treatment with an investigational drug within 1 month of enrolment
  • Any contra-indication to regular wound care
  • Inability or unwillingness to consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Judy Dan Centre for Hyperbaric Medicine & Advance Wound Care

North York, Ontario, M2R 1N5, Canada

Location

MeSH Terms

Conditions

Wounds and Injuries

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 7, 2021

First Posted

January 11, 2022

Study Start

February 24, 2022

Primary Completion

December 1, 2022

Study Completion

December 1, 2022

Last Updated

June 25, 2026

Record last verified: 2026-06

Locations