EUCTR2004-002296-16-ES进行中（未招募）不适用
Ensayo para evaluar la eficacia, seguridad y tolerabilidad, de una estrategia de simplificacion temprana a Trizivir, en pacientes con supresion virologica tras tratamiento antiretroviral con Combivir mas Lopinavir/Ritonavir (Kaletra).
Antonio Antela López0 个研究点目标入组 142 人开始时间: 2005年5月11日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 142
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. Diagnosed confirmed of HIV infection.
- •2. age > 18 years
- •3. Naïve patients to ARVT.
- •4. CD4 cels < 200 cels /mm3
- •5. Patient clinically stable.
- •6. Patient signd up the informed consent form
- •7. Pregnancy test at time of baseline negative
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Two barrier contraception methods if childbearing potential for fertil women.
- •2. Active AIDS as defined by CDC international clasification 1993.
- •3. Active mediical condition at time of baseline that intarects with the medical status of the patient and tha HIV treatment.
- •4. Patients with antineoplasic, inmunomodulator or radiotoxic in investigational phase.
- •5. Patients in present investigational treatment or need it.
- •6. Alcohol and/or drug abusewich could interfere with study drugs.
- •7. Netrophile count under 75.000 mg/l or Hemoglobine under 4.65 mmol/L
- •8. patient who might be prescribed of any nota loowed concomitnt drug
- •9. Hypersensibility to any excipient of the study drug.
研究者
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