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临床试验/NCT05105139
NCT05105139已完成不适用

Retrospective Study to Evaluate the Safety of Sebryl® and / or Sebryl Plus® in the Treatment of Seborrheic Dermatitis and Psoriasis of the Scalp in Routine Medical Practice.

Laboratorios Silanes S.A. de C.V.1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年11月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
90
试验地点
1
主要终点
Classify adverse events

研究概览

简要总结

Observational, descriptive, retrospective, multicenter study to evaluate the safety of the treatment with Sebryl® and / or Sebryl Plus® in the management of seborrheic dermatitis and psoriasis of the scalp in routine medical practice.

详细描述

The objective of this study is to evaluate the frequency and intensity of adverse events presented during treatment with Sebryl® and / or Sebryl Plus® for the management of seborrheic dermatitis and psoriasis of the scalp. The sample will be at convenience. The files of the patients who have received treatment with Sebryl® and / or Sebryl Plus® in the last 5 years (2016 to 2021) will be chosen.

The researchers or the personnel designated by them will capture the information recorded by the treating physicians in the clinical file, sociodemographic, clinical and safety data that were presented after the prescription of Sebryl® and / or Sebryl Plus®.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Treatment with Sebryl® and / or Sebryl Plus® documented, for at least 2 consultations.
  • That the patient has been questioned about possible adverse events

排除标准

  • That the patient has used some other concomitant treatment for seborrheic dermatitis and psoriasis on the scalp.

结局指标

主要结局

Classify adverse events

时间窗: Last 5 years

Classify reported adverse events according to seriousness, severity (intensity) and causality of the clinical manifestation

Describe study population by gender ratio

时间窗: Last 5 years

Describe the proportion of women and men included in the study

Proportion of adverse events

时间窗: Last 5 years

Evaluate the presence or absence of adverse events reported in the clinical files.

Mean age in years

时间窗: Last 5 years

Describe the mean age in years of the patients included in the study.

Describe the body mass index through weight and heigh

时间窗: Last 5 years

Describe the body mass index of the study population calculated through weight and heigh of the patient and using the formula kilogram over square meter.

Mean heart rate in beats per minute

时间窗: Last 5 years

Describe the mean heart rate in beats per minute of the patients included in the study.

Describe the blood pressure millimetres of mercury (mmHg)

时间窗: Last 5 years

Describe the blood pressure in mmHg of the patients included in the study.

Percentage of times use outside of expected indications

时间窗: Last 5 years

Percentage of times Sebryl® and / or Sebryl® Plus were used outside of expected indications.

次要结局

  • Description of usage pattern according to prescribed time(Last 5 years)
  • Description of usage pattern according to prescribed dosage(Last 5 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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