deltatrials
Suspended PHASE2/PHASE3 INTERVENTIONAL 2-arm NCT00717652

Efficiency And Safety Of Association Arbutin, Triamcinolone And Tretinoin In Treatment Of Melasma (melasma)

Efficiency And Safety Of Association Arbutin, Triamcinolone And Tretinoin In The Treatment Of Facial Melasma, Taking As Reference The Product Triluma ® (Hidroquinone, Fluoncinolone And Tretinoin).

Sponsor: Azidus Brasil

Conditions Melasma
Updated 7 times since 2017 Last updated: Nov 1, 2022 Started: Jul 31, 2008 Primary completion: Jul 31, 2008 Completion: Jul 31, 2008
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Suspended

This trial was suspended. No reason was provided.

A PHASE2/PHASE3 clinical study on Melasma, this trial is suspended. The trial is conducted by Azidus Brasil and has accumulated 7 data snapshots since 2008. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Study Description(click to expand)

The melasma is a common hipermelanosis, acquired, symmetrical, with irregular occurring in areas such as photo-exposed face, forehead and temples, can affect the eyelids and tion. The facial regions most affected are: zigomatic (82.4%), parotid (64.7%), front (64.7%), mandible (35.3%) and nasal (35.3%). The injuries of melasma is variable increase of epidermal melanin and inflammatory infiltrate of mild to moderate intensity. Treatment with compounds such as hydroquinone and derivatives, tretinoin, corticosteroids moderate or combination of them all have shown good results, diminishing the training, reducing the stability and promoting the destruction of melanocytes. The primary objective of this study is evaluating the clinical activity of the association (tretinoin + arbutin + triamcinolone) manufactured by Glenmark Laboratory, and as the comparator drug product Triluma ® (hydroquinone + fluocinolone + tretinoin), in the treatment of epidermal melasma through parameters of clinical course of the disease (improves) and its security. Patients who are included in the study will be randomly and automatically receive one of the treatments (New association or Triluma ®), which should use for 12 weeks. The products should be applied in the regions affected once a day, during night. The evaluation of clinical improvement, as well as security, will be...

The melasma is a common hipermelanosis, acquired, symmetrical, with irregular occurring in areas such as photo-exposed face, forehead and temples, can affect the eyelids and tion. The facial regions most affected are: zigomatic (82.4%), parotid (64.7%), front (64.7%), mandible (35.3%) and nasal (35.3%). The injuries of melasma is variable increase of epidermal melanin and inflammatory infiltrate of mild to moderate intensity. Treatment with compounds such as hydroquinone and derivatives, tretinoin, corticosteroids moderate or combination of them all have shown good results, diminishing the training, reducing the stability and promoting the destruction of melanocytes. The primary objective of this study is evaluating the clinical activity of the association (tretinoin + arbutin + triamcinolone) manufactured by Glenmark Laboratory, and as the comparator drug product Triluma ® (hydroquinone + fluocinolone + tretinoin), in the treatment of epidermal melasma through parameters of clinical course of the disease (improves) and its security.

Patients who are included in the study will be randomly and automatically receive one of the treatments (New association or Triluma ®), which should use for 12 weeks. The products should be applied in the regions affected once a day, during night.

The evaluation of clinical improvement, as well as security, will be held on periodic visits, as described below, which will be held the record and supply of medicines to patients.

In each visit, beyond the clinical examination of photographs and large, it filled the Area and Severity Scale (Melasma Area and Severity Index - MASI), which quantifies the melasma and will be the main tool of control of clinical improvement.

At the end of the study, data will be compared, showing no inferiority or inferiority of clinical drug testing in relation to the comparator.

Status Flow

~Jan 2017 – ~Jun 2018 · 17 months · monthly snapshotSuspended~Jun 2018 – ~Jan 2021 · 31 months · monthly snapshotSuspended~Jan 2021 – ~Dec 2022 · 23 months · monthly snapshotSuspended~Dec 2022 – ~Jul 2024 · 19 months · monthly snapshotSuspended~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotSuspended~Sep 2024 – present · 19 months · monthly snapshotSuspended~Jan 2026 – present · 3 months · monthly snapshotSuspended

Change History

7 versions recorded
  1. Jan 2026 — Present [monthly]

    Suspended PHASE2/PHASE3

  2. Sep 2024 — Present [monthly]

    Suspended PHASE2/PHASE3

  3. Jul 2024 — Sep 2024 [monthly]

    Suspended PHASE2/PHASE3

    Phase: PHASE2_PHASE3PHASE2/PHASE3

  4. Dec 2022 — Jul 2024 [monthly]

    Suspended PHASE2_PHASE3

  5. Jan 2021 — Dec 2022 [monthly]

    Suspended PHASE2_PHASE3

Show 2 earlier versions
  1. Jun 2018 — Jan 2021 [monthly]

    Suspended PHASE2_PHASE3

  2. Jan 2017 — Jun 2018 [monthly]

    Suspended PHASE2_PHASE3

    First recorded

Jul 2008

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Azidus Brasil
Data source: Azidus Brasil

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations