The Transmission of Artemisinin Resistant Parasites Before and After Conventional Artemisinin-combination Therapy
Launched by INFECTIOUS DISEASES RESEARCH COLLABORATION, UGANDA · Mar 29, 2024
Trial Information
Current as of July 16, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how well conventional malaria treatments work against parasites that have become resistant to the main malaria drugs called artemisinins. Researchers will recruit patients with uncomplicated malaria who are being treated with standard combination therapies in a clinic. They will look at the ability of these resistant parasites to spread before, during, and after treatment. Participants will be monitored closely for seven days to see how well the treatment clears the infection and how it impacts the transmission of the disease.
To be eligible for the trial, participants must be at least 2 years old and have been diagnosed with a specific type of malaria called P. falciparum, confirmed by a blood test. They should also have a fever or recent history of fever and be able to take oral medication. Participants will receive supervised treatment and will have their progress checked regularly. This study is important because it aims to understand how resistant malaria strains behave, which can help improve future treatments and control the spread of malaria.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • age ≥2 years
- • blood smear positive for P. falciparum gametocytes
- • mono-infection with P. falciparum confirmed by positive blood smear;
- • parasitaemia of \>100 P. falciparum asexual forms/µL;
- • ability to swallow oral medication;
- • ability and willingness to comply with the study protocol for the duration of the study and to comply with the study visit schedule;
- • informed consent from parent or guardian;
- • haemoglobin ≥ 7.0 g/dl for children below 10 years of age or ≥8.0g/dL for older individuals
- Exclusion Criteria:
- • presence of general danger signs;
- • mixed or mono-infection with another Plasmodium species detected by microscopy;
- • presence of severe malnutrition defined as a very low weight for height (below -3z scores of the median WHO growth standards), by visible severe wasting, or by the presence of nutritional oedema.
- • presence of febrile conditions due to diseases other than malaria (e.g. measles, acute lower respiratory tract infection, severe diarrhoea with dehydration) or other known underlying chronic or severe diseases (e.g. cardiac, renal and hepatic diseases, HIV/AIDS);
- • history of hypersensitivity reactions or contraindications to any of the medicine(s) being tested
About Infectious Diseases Research Collaboration, Uganda
The Infectious Diseases Research Collaboration (IDRC) in Uganda is a leading clinical trial sponsor dedicated to advancing public health through innovative research in infectious diseases. Operating at the intersection of science and community engagement, IDRC conducts rigorous clinical trials and epidemiological studies aimed at understanding and combating infectious diseases prevalent in Uganda and beyond. With a multidisciplinary team of researchers, clinicians, and public health experts, IDRC collaborates with local and international partners to generate high-quality evidence that informs health policies and practices, ultimately improving health outcomes for vulnerable populations. Through its commitment to ethical research and capacity building, IDRC plays a pivotal role in addressing the challenges posed by infectious diseases in the region.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Kalongo, Agago District, Uganda
Patongo, Agago District, Uganda
Patients applied
Trial Officials
Teun Bousema, PhD
Principal Investigator
London School of Hygiene and Tropical Medicine
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported