CTRI/2024/03/064108尚未招募3 期
acetyl cysteine therapy in patients with Pulmonary tuberculosis: A Pilot Open- Label Randomized controlled trial - NI
Dr Saurabh Mittal0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Age 18 years or more.
- •2.Willing to give written informed consent.
- •3.Body weight = 30 kg.
- •4.Pulmonary TB diagnosed with One sputum OR Bronchoalveolar lavage GeneXpert test positive.
- •5.No detection of Rifampicin resistance by GeneXpert/ LPA/ MGIT C/S.
- •6.A chest radiograph abnormality consistent with tuberculosis.
- •7.No prior history of ATT.
- •8.Willing to undergo HIV serology testing.
- •9.Agrees to use effective barrier contraception during the period of the study.
- •10.Residing around the study site (AIIMS, Delhi).
- •11.Express willingness to attend the treatment center for supervised treatment.
- •12.Express willingness to adhere to the trial procedures and follow-up schedule.
排除标准
- •1.Clinically significant evidence of extrapulmonary TB (miliary TB, abdominal TB, urogenital TB, osteoarthritic TB, TB meningitis).
- •2.Poor general condition as assessed by the study investigator.
- •3.Renal dysfunction including (but not limited to) serum creatinine levels above the upper limit of the laboratory reference range (Serum creatinine >1.2 mg/dL or blood urea >43 mg/dL)
- •4.Has clinical jaundice or hepatic impairment characterized by serum bilirubin level above 1.2 times upper limit of the laboratory reference range, or by alanine aminotransferase (ALT) and/ or aspartate aminotransferase (AST) levels >3 times the upper limit of the laboratory reference range
- •5.Diabetes mellitus or Psychiatric illness
- •6.Serology positive for HBSAg Or Hepatitis C virus antibody Or HIV
- •7.Pregnant or lactating females
- •8.Has any condition (social or medical) which in the opinion of the investigator would make trial participation unreliable or unsafe
- •9.Active drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements
- •10.Has a known allergy to any of the drugs proposed to be used in the trial regimen
- •11.Has evidence of clinically significant metabolic, gastrointestinal, neurological, psychiatric or endocrine diseases, malignancy, or other abnormalities.
研究者
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