Evaluation of the Efficacy of Artemisinin Combination Therapy in Kenya
- Conditions
- Malaria
- Interventions
- Registration Number
- NCT01899820
- Lead Sponsor
- Sabah Ahmed Omar
- Brief Summary
Artemisinin-based combination therapies (ACTs) are recommended for use against uncomplicated malaria in areas of multi-drug resistant malaria. The Ministry of Health, Division of Malaria Control (DOMC) rolled out the use of artemether-lumefantrine as the first line treatment for uncomplicated malaria in 2006.The development of the ACTs and its derivatives are the most rapidly acting of all the current antimalarial drugs and recognition of their potential role as a component of combination therapy have led to several large trials aimed at assessing different combinations of existing drugs, and to the specific development of new combination drugs.
This proposal aims to (1) evaluate the efficacy of artemisinin-based anti-malaria combination drugs in different sites across Kenya (2) elucidate the markers of resistance to ACTs through molecular genetics and in this process further strengthen capacity in the proposed study sites as well as improve links between research and control ultimately to influence malaria treatment policy and practice.
Five groups in East Africa will conduct a multi-centre, randomised, two arm trial to assess the efficacy of dihydroartemisin-piperaquine with artemether-lumefantrine as the comparative drug. The network will determine antimalarial drug efficacy using standardised protocols and collate clinical responses and adverse events. Molecular markers to artemisinin resistance will be investigated by molecular sequencing and comparison of parasite profiles in drug failure cases. Recrudescence or re-infections will be differentiated by analysis of the MSP1, MSP2 and GLURP genes and assess transmission dynamics post treatment. Data from these studies will be captured into a database developed by the network. The latter offers several advantages including
* Working towards the standardization of methodologies and common protocols as a way of comparing data across sites
* Pulling together datasets and conduct a multi-centre analysis
* Sharing and coordinating quality assurance mechanisms
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 2100
- Age between 6 months - 5 years (in high endemic areas); 6 months to 10 years (in low endemic areas) inclusive.
- Presence of axillary temperature > 37.5oC or rectal / tympanic temp > 38.0oC, or history of fever in the last 24 hours.
- Monoinfection with Plasmodium falciparum with parasitaemia, asexual parasitemia between 2,000 - 200,000 p/µl (in areas of high transmission); 1,000-100,000p/ µl (in areas of low to moderate malaria transmission)
- Ability and willingness to comply with the study protocol for the duration of the study and to comply with the study visit schedule; and
- Signed informed consent form by the parents or legal guardian.
- Presence of clinical danger signs: not able to drink or breast-feed, vomiting (>twice in 24 hours), recent history of convulsions (>1 in 24h), unconscious state, unable to sit or stand;
- Mixed or mono-infection with another Plasmodium species detected by microscopy;
- Presence of co-morbid infection (e.g. acute lower respiratory tract infection, severe diarrhoea with dehydration, Severe Anaemia) or other known underlying chronic or severe diseases (e.g. cardiac, renal and hepatic diseases,Epilepsy, HIV/AIDS);
- History of hypersensitivity reactions or contraindications to any of the medicine(s) being tested or used as alternative treatment(s).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Artemether lumefantrine Artemether lumefantrine Tablets, 1-4 tablets (weight calculated dose), BD, at hr 0, 8, 24, 36, 48 and 60. Dihydroartemisinin piperaquine Dihydroartemisinin piperaquine Tablets, 2 paediatric tablets/1 adult tablet, OD, every 24 hours for 48 hours
- Primary Outcome Measures
Name Time Method The primary endpoint will be the PCR-corrected and parasitological response (PCR corrected ACPR) at days 28 and 42. Change in this outcome measure will be assessed. Day 28 and day 42 ACPR is defined as the absence of parasitaemia on day 42 irrespective of the temperature without previously meeting any of the criteria of early treatment failure or late clinical or parasitological failure.
Patients with late asexual parasite reappearance will be considered ACPR if the CR analyses shows a new infection rather than a recrudescence (through PCR genotyping).
The total treatment failure is defined according to the WHO criteria as the sum of early and late treatment failures.
- Secondary Outcome Measures
Name Time Method Heart rate Up to day 42 Respiratory rate Up to day 42 Crude (PCR uncorrected) ACPR ratio at day 28 (PCR uncorrected ACPR) Day 28 Fever Clearance Time (FCT) 0 to 48 hours This will be defined as the time (hrs) from the start of a patient's treatment to the first consecutive axillary temp measurements below 37.5 for at least 48 hrs
Comparison between adverse events related to artemether lumefantrine and dihydroartemisinin piperaquine Up to day 42 Temperature Up to day 42 Oxygen saturation Up to day 42 Cure ratios at day 28, 42, (PCR corrected and PCR uncorrected). Change in this outcome measure will be assessed. Day 28 and day 42 Changes of haemoglobin (Hb) concentration from day 0 to days 28, and 42 Day 0, day 28 and day 42 Number of participants with adverse events Up to day 42 Asexual parasite clearance time (PCT) Day 0 to day 28, upto day 42 PCT(proportion of patients remaining parasitaemic) defined as the time (in hours) from the start of a patient's treatment to 2 consecutive negative blood slides (collected at different days)
Gametocyte carrier rates and geometric mean densities (excluding negatives) will be compared on days 7, 14, 28 and 42. Change in this outcome measure will be assessed. Day 7, 14, 28 and 42
Trial Locations
- Locations (7)
Msambweni sub-district hospital
🇰🇪Msambweni, Kwale, Kenya
Kitale district hospitals
🇰🇪Kitale, Kenya
Machakos district hospital
🇰🇪Machakos, Kenya
Nyando district hospital
🇰🇪Nyando, Kenya
Malindi district hospitals
🇰🇪Malindi, Kenya
Busia district hospitals
🇰🇪Busia, Kenya
Kisii district hospitals
🇰🇪Kisii, Kenya