AI Article Synopsis

  • Increased cases of toxoplasma encephalitis in AIDS patients with low CD4+ counts have led to the investigation of the effectiveness of sulfonamide combinations due to limited access to traditional treatments in China.
  • This study will compare the effects of a readily available sulfonamides formulation plus clindamycin with the standard TMP-SMX plus azithromycin treatment over a 48-week follow-up period involving 200 participants.
  • The trial aims to establish reliable evidence regarding the new treatment's efficacy and safety for AIDS patients suffering from toxoplasma encephalitis.

Article Abstract

Background: An increased frequency of toxoplasma encephalitis, caused by Toxoplasma gondii, has been reported in AIDS patients, especially in those with CD4+ T cell counts <100 cells/μL. Several guidelines recommend the combination of pyrimethamine, sulfadiazine, and leucovorin as the preferred regimen for AIDS-associated toxoplasma encephalitis. However, it is not commonly used in China due to limited access to pyrimethamine and sulfadiazine. The synergistic sulfonamides tablet formulation is a combination of trimethoprim (TMP), sulfadiazine and sulfamethoxazole (SMX), and is readily available in China. Considering its constituent components, we hypothesize that this drug may be used as a substitute for sulfadiazine and TMP-SMX. We have therefore designed the present trial, and propose to investigate the efficacy and safety of synergistic sulfonamides combined with clindamycin for the treatment of toxoplasma encephalitis.

Methods/design: This study will be an open-labeled, multi-center, prospective, randomized, and controlled trial. A total of 200 patients will be randomized into TMP-SMX plus azithromycin group, and synergistic sulfonamides plus clindamycin group at a ratio of 1:1. All participants will be invited to participate in a 48-week follow-up schedule once enrolled. The primary outcomes will be clinical response rate and all-cause mortality at 12 weeks. The secondary outcomes will be clinical response rate and all-cause mortality at 48 weeks, and adverse events at each visit during the follow-up period.

Discussion: We hope that the results of this study will be able to provide reliable evidence for the efficacy and safety of synergistic sulfonamides for its use in AIDS patients with toxoplasma encephalitis.

Trial Registration: This study was registered as one of 12 clinical trials under the name of a general project at chictr.gov on February 1, 2019, and the registration number of the general project is ChiCTR1900021195. This study is still recruiting now, and the first patient was screened on March 22, 2019.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253700PMC
http://dx.doi.org/10.1097/MD.0000000000020146DOI Listing

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