跳至主要内容
临床试验/EUCTR2020-000720-19-IT
EUCTR2020-000720-19-IT进行中(未招募)1 期

A prospective, randomized, multicenter, open- label, two-arm and parallel-group Study to evaluate the efficacy and safety of Nicotinamide DS compared to Ciclopirox olamine cream at 1% in patients affected by seborrheic dermatitis. - IDI01/2020

IDI FARMACEUTICI SR0 个研究点目标入组 102 人开始时间: 2021年5月24日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
102

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.Male and female, = 18 years;
  • 2.Established diagnosis of seborrheic dermatitis of the face and scalp;
  • 3.Able to co-operate and understand written and oral information;
  • 4.Written informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 68
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 34

排除标准

  • 1. Concomitant dermatological diseases (eg acne, rosacea, contact dermatitis)
  • 2. Recent use of treatments for seborrheic dermatitis (2 weeks for topical treatments; 4 weeks for systemic treatments);
  • 3. Hypersensitivity to the active substance or to any of the excipients;
  • 4. Established diagnosis of Actinic keratosis;
  • 5. Established diagnosis of Parkinson;
  • 6. Established diagnosis of HIV infection;
  • 7. Use of immunesuppressant medications since last three months;
  • 8. Established diagnosis of cardiac diseases;
  • 9. Established diagnosis of alcoholic pancreatitis;
  • 10. Established diagnosis of other neurological diseases;
  • 11. Established diagnosis of Diabetic;
  • 12. Pregnancy (positive pregnancy test for women of childbearing potential) and lactation;
  • 13. Participation in any other clinical Study within 3 months prior to screening.

研究者

发起方
IDI FARMACEUTICI SR

相似试验

招募中
不适用
Compare Sequential and Quadruple Therapy for the Eradication of Helicobacter pylori in KoreaCertain infectious and parasitic diseases
KCT0001176Seoul National University Bundang Hospital390
进行中(未招募)
1 期
A multi-centre, randomised, prospective, open-label study to investigate the efficacy and safety of a standardised correction dosage regimen of intravenous ferric carboxymaltose (FERINJECT®) versus iron sucrose (VENOFER®) for treatment of iron deficiency anaemia in patients with inflammatory bowel disease Estudio aleatorizado, multicéntrico, prospectivo y abierto para investigar la eficacia y la seguridad de una pauta de dosis de corrección normalizada de carboximaltosa férrica (FERINJECT®) administrada por vía intravenosa en comparación con sacarosa férrica (VENOFER®) para el tratamiento de la anemia ferropénica en pacientes con enfermedad inflamatoria intestinal
EUCTR2008-002333-75-ESVifor (International) Inc.420
进行中(未招募)
不适用
A multi-centre, randomised, prospective, open-label study to investigate the efficacy and safety of a standardised correction dosage regimen of intravenous ferric carboxymaltose (FERINJECT®) versus iron sucrose (VENOFER®) for treatment of iron deficiency anaemia in patients with inflammatory bowel diseaseIron deficiency anaemia in patients with inflammatory bowel diseaseMedDRA version: 9.1Level: LLTClassification code 10055736Term: Iron deficiency anaemia secondary to blood loss (chronic)
EUCTR2008-002333-75-ATVifor (International) Inc.420
进行中(未招募)
不适用
A multi-centre, randomised, prospective, open-label study to investigate the efficacy and safety of a standardised correction dosage regimen of intravenous ferric carboxymaltose (FERINJECT®) versus iron sucrose (VENOFER®) for treatment of iron deficiency anaemia in patients with inflammatory bowel disease
EUCTR2008-002333-75-EEVifor (International) Inc.420
进行中(未招募)
不适用
A multi-centre, randomised, prospective, open-label study to investigate the efficacy and safety of a standardised correction dosage regimen of intravenous ferric carboxymaltose (FERINJECT®) versus iron sucrose (VENOFER®) for treatment of iron deficiency anaemia in patients with inflammatory bowel diseaseIron deficiency anaemia in patients with inflammatory bowel diseaseMedDRA version: 9.1Level: LLTClassification code 10055736Term: Iron deficiency anaemia secondary to blood loss (chronic)
EUCTR2008-002333-75-DEVifor (International) Inc.420