Optimising Operational Use of Artemether-lumefantrine Comparing 3 Day Versus 5 Day

Plasmodium Falciparum Infection Clinical Trial

— AL3vs5  

Official title:

An Open-label Randomized Controlled Trial to Evaluate the Effectiveness and Safety of a 3 Day Versus 5 Day Course of Artemether-lumefantrine for the Treatment of Uncomplicated Falciparum Malaria in Myanmar

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02020330
• Other study ID #: MOCRU1301
• Status: Completed
• Phase: Phase 3
• Start date: November 25, 2013
• Est. completion date: March 25, 2015

Study information

• Verified date: September 2018
• Source: University of Oxford
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomised two arm study, comparing artemether-lumefantrine 3 days and 5 days treatment. Patients will be randomised in blocks of ten to one of the two treatment arms. The standard regimen is twice daily for three days with a delay of at least eight hours between the first and second doses. A single of primaquine will be given to all patients on the first day of treatment for gametocytocidal activity. The initial treatment will be given under supervision, all other subsequent doses will be given to the patient to the taken at home. Patients will be followed up for nine visits over forty two days.

Description:

• The study will be conducted in 6 village health centres in the Mon and Kayin states

• The patient or parent/guardian (in case of minor or under aged) must personally sign and date the latest approved version of the informed consent form before any study specific procedures are performed

• A case record form will be completed for each patient documenting symptoms prior to clinic attendance, concomitant illness, drug history. Height, weight, vital signs and physical examination findings will be recorded.

• At enrolment (D0) all patients will have the following samples taken:

• Repeat parasite count (thick and thin films). Treatment should be started without waiting for the result.

• Filter paper blood blots (3 dots on Whatman 3MM filter paper approx 180-300 µL blood) for parasite genotyping (MSP1, MSP2, GLURP in case of recurrence during follow-up)

• Haemoglobin

• Laboratory procedures

• Slide microscopy: Thick and thin blood films stained with Giemsa will be read and counts expressed as the number of parasites per 500 white blood cells

• Molecular studies: The samples will be used to detect asexual parasites (blood smear, sensitive PCR), parasite population structure (Sequenom genotyping and sequencing), gametocytes (microscopy). The samples will be stored in a cool box and kept maximum 5 days in the field and will be transported to the local laboratory for processing. Plasma and buffy coat will be separated, frozen and stored. The frozen packed red cells will be transported to the molecular laboratory at MORU, Bangkok, Thailand, for sample processing (DNA extraction, quantitative PCRs).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: March 25, 2015
• Est. primary completion date: February 4, 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Years and older

Eligibility

Inclusion Criteria:

1. Age = 6 year

2. Symptomatic malaria infection, i.e. history of fever or presence of fever >37.5°C

3. Microscopic confirmation of asexual stages of P. falciparum (may be mixed with non-falciparum species) with parasitaemia PFT=5/500 WBC

4. Written informed consent given to participate in the trial

Exclusion Criteria:

1. Pregnancy or lactation (urine test for ß HCG to be performed on any woman of child bearing age unless menstruating).

2. Female of 12 to 18 years of age

3. P. falciparum asexual stage parasitaemia greater than or equal to 4% red blood cells (175,000/µL).

4. Signs or symptoms indicative of severe malaria including:

• Impaired consciousness (Blantyre Coma Score <5 or Glasgow Coma Scale <15)

• Severe anaemia (Hb% <5 mg/dl)

• Bleeding disorder -evidenced by epistaxis, bleeding gums, frank haematuria, bleeding from venepuncture sites

• Respiratory distress

• Severe jaundice

• Haemodynamic shock

5. A full course of artemether-lumefantrine treatment in the previous 28 days

6. Known hypersensitivity to artemisinins - defined as history of erythroderma/other severe cutaneous reaction, angioedema or anaphylaxis

7. History of splenectomy

Related Conditions & MeSH terms

• Plasmodium Falciparum Infection

Intervention

Drug:
• Artemether-lumefantrine 3 days
One tablet contains 20mg artemether and 120mg lumefantrine. The standard regimen is twice daily for 3 days with a delay of at least 8 hours between the first and second dose. It is dosed by weight categories. One gram of fish oil will be given to half of the participants in the 3 days arm.
• Artemether-lumefantrine 5 days
One tablet contains 20mg artemether and 120mg lumefantrine. The experiment regimen is twice daily for 5 days with a delay of at least 8 hours between the first and second dose. It is dosed by weight categories. One gram of fish oil will be given to half of the participants in the 5 days arm.

Locations

Country	Name	City	State
Myanmar	Medical Action Myanmar	Yangon

Sponsors (1)

Lead Sponsor	Collaborator
University of Oxford

Country where clinical trial is conducted

Myanmar, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	proportion of patients with detectable parasitaemia	Assessed by sensitive PCR on days 5 and 7 after treatment	On day 5 and day 7
Secondary	Parasitaemia clearance time	Assessed by sensitive PCR on D3 in the 3 day arm and D5 in the 5 day arm	On day 3 and Day 5
Secondary	Gametocyte carriage rates		Day 7
Secondary	artemether-lumefantrine tolerability	Tolerability of artemether-lumefantrine will be assessed by comparing the proportion of patients with anorexia, nausea, vomiting, abdominal pain and other symptoms of administration between the intervention arm and the control arm	5 days
Secondary	Comparison of effectiveness	Comparison of effectiveness uncorrected and corrected will be assessed by PCR genotyping	Day 42
Secondary	concentrations of lumefantrine		Day 7
Secondary	Haematological recovery rate	Assessed by comparing hemoglobin between baseline and after treatment at day 28	Day 28
Secondary	Incidence of vivax malaria relapses	Assessed by the microscopist find malaria smear positive within the follow up period	42 days
Secondary	Comparison of addition of food supplement (fish oil)	Assessed by comparing lumefantrine concentration on day 7 and proportion of patients with detectable parasitaemia by qPCR	day 3 to day 21