National Department of Health
Port Moresby, Papua New Guinea
NCT Number: NCT05764876
The goal of this clinical trial is to test the non inferiority of linezolid compared with azithromycin as a treatment for yaws . The main questions it aims to answer are: can linezolid cure active yaws, and can linezolid cure latent yaws. Participants with serologically confirmed yaws will be randomized to receive linezolid (experimental) or azithromycin (control group) treatment and followed up to assess clinical resolution.
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Notify Me5 year–18 year
All sexes
Interventional
Phase 3
Port Moresby, Papua New Guinea
The current principle of yaws eradication is based on a single round of mass drug administration of azithromycin (AZI) called total community treatment (TCT) followed by targeted treatment of active cases and close contacts every 6 months called total targeted treatment (TTT). Studies done in Papua New Guinea have shown that 3 rounds of TCT are preferable to 1 TCT followed by TTT rounds because it results in higher overall coverage, particularly of latent cases. In the context of repeated rounds of TTT and multiple rounds of TCT, resistance to AZI has ben detected on 5 patients with yaws Recent studies have been successful on the culture of Treponema pallidum (syphilis and yaws), therefore investigators are now able to identify more potential treatment for yaws and syphilis.
Yaws is one of the major causes of the Cutaneous Ulcer Disease (CUD) syndrome. The CUD syndrome is a painful and debilitating condition, endemic to remote tropical regions with poor sanitation and limited health care access affecting children mainly. In Papua New Guinea it is caused by a range of unknown and some known pathogens besides yaws that are not easily distinguished on clinical diagnosis. New information on the causative agents of the CUD syndrome is needed to facilitate its management with an integrated approach.
The aim of the project is to provide evidence supporting (or rejecting) the hypothesis that the use of linezolid (LZD) can be an alternative treatment to cure yaws corroborated by clinical, serological, and molecular methods. LZD is a very safe drug that has been delivered to adults and children for the treatment of cutaneous infections all over the world. Investigators will compare two different treatments: (A) linezolid (LZD) and (B) azithromycin (AZI). In addition, the investigators plan to contribute to characterize the etiology of the CUD syndrome. The study will be implemented in selected wards of the Islands Region of Papua New Guinea.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Oral tablet of linezolid
Other names: Zyvox, Zyvoxid
Oral tablet of azithromycin 30mg/kg maximum 2gr single dose.
Other names: Zithromax
Time frame: 4 weeks after treatment
Proportion of patients with clinical resolution of yaws lesions (clinical cure). Assessment of clinical resolution defined as the complete healing of lesions at 4 weeks from treatment start.
Time frame: 24 weeks after treatment
Proportion of patients with adequate serological response (serological cure). Assessment of sero-cure is described as a negative DPP test at 24 weeks from treatment start.
Time frame: 24 weeks after treatment
Proportion of patients with relapse (recurrent episodes caused by the same strain) (molecular cure). Assessment of recurrence by molecular methods of Treponema pallidum ssp. pertenue (TPE) DNA in ulcer swab to determine relapse or reinfection within 24 weeks from treatment start.
Time frame: Baseline (before treatment)
Assessment of TPE strains by genomic molecular methods in ulcer swabs from patients with active yaws.
Time frame: Baseline (before treatment)
Assessment of TPE strains by genomic molecular methods in oral swabs from patients with active/latent yaws.
Time frame: Baseline (before treatment)
Assessment of TPE strains by genomic molecular methods in plasma from patients with active/latent yaws.
Time frame: Baseline (before treatment)
Proportion of patients with allelic variation in TPE DNA in patients with recurrence or treatment failure.
Time frame: 4 weeks after treatment
Proportion of patients with antibiotic resistance genotype.
Time frame: Baseline (before treatment)
Proportion of patients with selected known and unknown causes of cutaneous ulcers (CU). Assessment of etiological agents using polymerase chain reaction (PCR) for TPE, Haemophylus ducreyi (HD) and Streptoccocus pyogenes (SP).
Time frame: at 4 and up to 24 weeks after treatment.
Proportion of patients with adverse events
Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
Other
Acronym: Trep-AByaws
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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