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Search / Trial NCT03478033

Rifampicin vs Rifabutin in HIV/AIDS Patients Combined With Tuberculosis

Launched by SHANGHAI PUBLIC HEALTH CLINICAL CENTER · Mar 20, 2018

Trial Information

Current as of April 28, 2025

Unknown status

Keywords

Tuberculosis Aids Rifampicin Rifabutin

ClinConnect Summary

Two hundreds and thirty participants will be randomly assigned to receive an anti--tuberculosis treatment include rifampicin or rifabutin for two months of intensive therapy. Isoniazid and rifampicin (or rifabutin) will be continued to use for four months of consolidation therapy. A total of followed up period will be 12 months.

The antiretroviral therapy(ART) include:

Tenofovir disoproxil fumarate 300mg/d +Lamivudine 300mg/d+ Efavirenz 600mg/d; or Zidovudine 300mg bid +Lamivudine 300mg/d +Efavirenz 600mg/d.

ART will be started after 2 weeks of anti-tuberculosis.

The follow-up visits in...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Age: 18-65 years old;
  • 2. No limited to gender;
  • 3. If anti-HIV-1 positive samples are detected by an initial test based on the ELISA method, they should be confirmed by western blot;
  • 4. The patients who are diagnosed with pulmonary TB (mycobacterium tuberculosis of sputum smear or culture was positive) but had never be treated;
  • 5. Sign informed consent form voluntarily, and guarantee to attend follow-up visits;
  • 6. Do not have plan to remove from the current experimental site during the trial process;
  • 7. The patients do not receive any antiretroviral treatment before;
  • 8. The overall situation of the patient should not affect the assessment and completion of the trial.
  • Exclusion Criteria:
  • 1. Patients with acute infection;
  • 2. During the screening period,patients with combined opportunistic infections and instability (National HIV/AIDS treatment guidelines) except for tuberculosis, or combined malignancy;
  • 3. During the screening period,hemachrome \< 6 g/dl, leukocyte \< 2000 /µl, neutrophils \< 1000 /µl, platelet count \< 75000 /µl, blood amylase is greater than two times the upper limit of normal, Scr is greater than1.5 times the upper limit of normal, AST/ALT/AKP is greater than two times the upper limit of normal, TBIL is greater than two times the upper limit of normal, serum CK is greater than two times the upper limit of normal;
  • 4. Now suffering from acute or chronic pancreatitis;
  • 5. Now suffering from peripheral neuritis;
  • 6. Pregnant and lactating women;
  • 7. Patients with severe mental and neurological diseases;
  • 8. Drug users;
  • 9. Patients with history of heavy drinking and cannot be terminated;
  • 10. Serious gastrointestinal ulcers;
  • 11. Atherosclerosis affects the arteries in the heart, brain or kidneys;
  • 12. Non-Chinese nationality;
  • 13. Now suffering from myopathy;
  • 14. Patients with previously treated tuberculosis.

About Shanghai Public Health Clinical Center

The Shanghai Public Health Clinical Center is a leading healthcare institution dedicated to advancing public health through innovative clinical research and trials. Renowned for its commitment to patient safety and ethical standards, the center specializes in a wide range of clinical studies aimed at improving disease prevention, diagnosis, and treatment. With a multidisciplinary team of experienced healthcare professionals and researchers, the center leverages cutting-edge technologies and methodologies to facilitate impactful research that addresses pressing public health challenges. By fostering collaboration with academic institutions and industry partners, the Shanghai Public Health Clinical Center plays a pivotal role in contributing to the global body of medical knowledge and enhancing health outcomes within the community.

Locations

Shanghai, Shanghai, China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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