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Completed

NCT Number: NCT00629317

Trial of Methyl Aminolevulinate Plus Aktilite in Facial Photodamage

The aim of the study is to determine the efficacy of MAL + Aktilite versus placebo + Aktilite in facial photodamage in a randomized double blind trial.

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Key information

Conditions

Age range

35 year–75 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

IPS Universitaria - Universidad de Antioquia

Medellín, Antioquia, 01, Colombia

About this study

It has been demonstrated that photodamage leads to wrinkles, mottled pigmentation, lentigines, telangiectasias, and textural changes, but more importantly, it can also lead to pre-cancerous conditions with the development of actinic keratosis (AK). The majority of photorejuvenation or photodamaged published studies have used 5-Amino-Levulinic acid (5-ALA) as a photosensitizer, and either a blue light or an Intense Pulsed Light source with a 70%-95% global facial skin improvement. The molecular mechanism of such improvement is unknown, but activation of a non-specific immune response in addition to increased fibrosis and new collagen formation, have both been suggested.

Methyl Aminolevulinate ( MAL) is another marketed photosensitizer mainly utilized in Europe. Lipophilicity, higher penetration depth and tumor selectivity has been advocated for MAL compared to 5-ALA. However, its effect in photodamaged skin has not been well documented.

The aim of the study is to determine the efficacy of MAL + Aktilite (PDT) in facial photodamage.

Study Type: Interventional

Study Design: Randomized, double-Blind, placebo-controlled trial. Official Title: A randomized, double-Blind, placebo-controlled trial of Methyl Aminolevulinate + Aktilite in patients with facial photodamage.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Female subjects older than 35 years of age and less than 75 years of age
  • Subjects with a photodamage grade of 2 or 3 according to a modified Dover´s Global photodamage scale
  • Subjects willing to participate according to protocol requirements.
  • Patients with signed Informed Consent
  • Patients with no exclusion criteria

Exclusion criteria

  • Pregnant or nursing females.
  • Subjects with suspected porphyria, Systemic or cutaneous erythematosus lupus, or any other photosensitizing disorder or drug induced photosensitization.
  • Any active infectious skin disorder ( Herpes simplex, molluscum contagiosum, facial warts )
  • Subjects with less than 6 months of previous rejuvenation interfering treatments
  • Subjects requiring concurrent treatment that would interfere with study objectives and/or assessments.

Treatment and study plan

Moisturizer

Other

Cetaphil cream(For 3 hours) + Aktilite ( Photodynamic Therapy for 8 minutes)

Other names: Cetaphil

Methyl Aminolevulinate

Drug

Methyl Aminolevulinate cream for 3 hours before Photodynamic therapy ( Aktilite)

Other names: Metvix

Primary outcomes

  1. Efficacy in facial global photodamage

    Time frame: 8 months

Secondary outcomes

  1. Facial fine lines, mottled pigmentation, tactile roughness, sallowness, erythema, telangiectasia

    Time frame: 12 months

  2. Histological effect of MAL+PDT in fibrosis and new collagen formation

    Time frame: 12 months

  3. Safety and tolerance

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Universidad de Antioquia

Other

Collaborators

  • Galderma R&D

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled Trial of Methyl Aminolevulinate + Aktilite in Patients With Facial Photodamage

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Mar 6, 2008
Registry last updated
Mar 16, 2009

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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