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OpenTrials
Completed

NCT Number: NCT02674048

Metvix Daylight PDT in Actinic Keratosis

Prospective non-interventional study conducted in Australia, Brazil, Mexico and Europe to evaluate clinical practice with Metvix Daylight PDT in the treatment of mild to moderate actinic keratosis of the face/scalp and to assess physician and patient satisfaction.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

See Jo-Ann, Sydney, New South Wales, Australia

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients to whom Metvix® Daylight-PDT has already been prescribed by their physician, according to the local label;

Treatment and study plan

Metvix

Other

Primary outcomes

  1. Percentage of physician satisfaction assessed on a 4-point scale from very satisfied to not satisfied with the question "Overall are you satisfied with Metvix DL-PDT?"

    Time frame: 3 months

  2. Percentage of patient satisfisfaction assessed on a 4-point scale from very satisfied to not satisfied with the question "Overall, how satisfied are you with this treatment?".

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Galderma R&D

Industry

Collaborators

  • Parexel

Registry information

Official study title

Observational Study to Evaluate Clinical Practice and Satisfaction With Metvix® Daylight Photodynamic Therapy (PDT) in the Treatment of Mild and/or Moderate Actinic Keratosis of the Face and/or the Scalp

Acronym: SESAME

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Feb 4, 2016
Registry last updated
Feb 17, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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