PER-064-11未知未知
EVALUATION OF RIFAPENTINE-CONTAINING REGIMEN FOR INTENSIVE PHASE TREATMENT OF PULMONARY TUBERCULOSIS
IVERSIDAD PERUANA CAYETANO HEREDIA,0 个研究点目标入组 8 人开始时间: 2011年9月30日最近更新:
试验速览
- 阶段
- 未知
- 发起方
- 入组人数
- 8
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 0(—)
入选标准
- •1. SUSPECTED PULMONARY TUBERCULOSIS WITH ACID-FAST BACILLI IN A STAINED SMEAR OF EXPECTORATED OR INDUCED SPUTUM POSITIVE (EXPECTORATED OR INDUCED). PATIENTS PRESENTING EXTRAPULMONARY TUBERCULOSIS ELIGIBLE IF THEY HAVE A POSITIVE SPUTUM CULTURE FOR PULMONARY TUBERCULOSIS. SPUTUM SPITTING TO BE OBTAINED BY NATURAL OR INDUCED; RESULTS OBTAINED RESPIRATORY SECRETIONS OR BRONCHIAL LAVAGE BE INVALID FOR ASSESSMENT OF ELIGIBILITY.
- •2. COMMITMENT TO ACCESS AN HIV TEST DONE IF YOUR HIV STATUS UNKNOWN OR THE LAST DOCUMENTED TEST WAS NEGATIVE 3 MONTHS BEFORE THE LISTING. REPEAT NOT BE NECESSARY IF HIV SEROLOGY WRITTEN DOCUMENTATION FOR A POSITIVE (ELISA AND WESTERN BLOT POSITIVE OR PLASMA VIRAL LOAD OVER 5000 COPIES / ML) BEFORE SUBMISSION.
- •3. FIVE (5) DAYS OR LESS OF MULTIPLE TUBERCULOSIS THERAPY IN THE 6 MONTHS PRIOR TO SUBMISSION.
- •4. SEVEN (7) DAYS OR LESS WITH A FLUOROQUINOLONE TREATMENT FOR 30 DAYS PRIOR TO THE INCLUSION.
- •5. AGE 18 YEARS.
- •6. SCORING SCALE OF 70 OR MORE KARNIOSFKY (CASUAL ATTENDANCE REQUIRED BUT IS CAPABLE OF CARRYING OUT THE MOST OF YOUR NEEDS, APPENDIX B).
- •7. INFORMED CONSENT SIGNATURE.
排除标准
- •1. PREGNANCY OR BREAST FEEDING.
- •2. INTOLERANCE KNOWN TO ANY OF THE STUDY DRUG.
- •3. DISEASE OR CONDITION CONCURRENT USE ISONIAZID CONTRAINDICATED (INH), RIFAMYCINS, PYRAZINAMIDE (PZA) OR ETHAMBUTOL (EMB). INCLUDED: SEVERE CHRONIC LIVER DISEASE, LIVER DISEASE FROM ANY CAUSE ACUTE AND Acute gouty arthritis.
- •4. ANTIRETROVIRAL CURRENT OR PLANNED DURING PHASE OF TUBERCULOSIS TREATMENT INTENSIVE OR CYCLOSERINE O TACROLIMUS. CYCLOSERINE AND UNACCEPTABLE TACROLIMUS INTERACTIONS WITH PRESENT RIFAMICINAS_
- •5. PULMONARY SILICOSIS.
- •6. CNS TUBERCULOSIS.
- •7. WEIGHT OF 40 KG OR LESS MORE THAN 85 KG.
研究者
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