EUCTR2009-016241-25-GR进行中（未招募）不适用
MULTICENTER, RANDOMIZED, DOUBLE-BLIND COMPARATIVE WITH THE REFERENCE PRODUCT CLINICAL STUDY TO DEMONSTRATE THE SAFETY AND EFFICACY OF THE THERAPY WITH THE COMBINATION ERYTHROMYCIN-ISOTRETINOIN/VERISFIELD, GEL, (2.0+0.05)% W/W FOR THE TOPICAL TREATMENT OF MILD TO MODERATE ACNE
VERISFIELD (UK) LTD, GREEK BRANCH0 个研究点开始时间: 2010年4月19日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •- PATIENTS WITH MILD TO MODERATE ACNE (ACNE VULGARIS)
- •- MALE AND FEMALE PATIENTS AGED 12-35 YEARS
- •- MALES AND FEMALES WHO ARE CONSIDERED HEALTHY
- •- FEMALE PATIENTS WHO DO NOT MANIFEST ANY SIGNS OF HYPERANDROGENISM
- •Are the trial subjects under 18? yes
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- PATIENTS WHO HAVE PARTICIPATED OR CURRENTLY PARTICIPATING IN ANOTHER STUDY
- •- PATIENTS ON TOPICAL OR SYSTEMIC TREATMENT FOR ACNE
- •- PATIENTS WHO RECEIVE DRUGS THAT MIGHT INFLUENCE THE FINDINGS OF THE STUDY
- •- PATIENTS WITH CARDIOVASCULAR, NEOPLASMIC, HAEMATOLOGICAL, HEPATIC, RENAL, NEUROLOGICAL, ENDOCRINE AND GASTROENTEROLOGICAL DISEASE
- •- PATIENTS WITH A DERMATOLOGICAL LESION IN THE AREA (OR IN CLOSE PROXIMITY e.g. 3cm) TO BE TREATED
- •- PREGNANT OR LACTATING PATIENTS
- •-FEMALE PATIENTS IN REPRODUCTIVE AGE WHO DO NOT RECEIVE ADEQUATE CONTRACEPTION
研究者
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