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NCT03181568

Evaluating Surface Area Reduction Using MolecuLight Imaging Device

Status unknown NA Last updated 9 June 2017
What this trial tests

NA trial testing MolecuLight i:X™ Imaging Device in Wound in 80 participants. Status unknown.

Timeline
10 July 2017
Primary endpoint
29 September 2017
29 September 2017

Quick facts

Lead sponsorCalver Pang
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposesupportive care
Enrollment80
Start date10 July 2017
Primary completion29 September 2017
Estimated completion29 September 2017
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Calver Pang

Who can join

18 and older, any sex, with Wound or Wound Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

12-week single-blind, prospective, randomized, controlled, pilot clinical trial assessing The MolecuLight i:X Imaging Device in chronic wounds. This device guides clinicians to inspect, sample, debride or further evaluate areas within or around a wound where potentially harmful bacteria appear under violet light illumination resulting in better overall care and accelerated surface area reduction compared to current standard care. The study aims to determine if this device aids in the healing of chronic wounds by reduction in size of wound compared to current standard of care.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Wound

Currently open trials in the same condition.

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Data sources for this page

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/NCT03181568.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing