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ARTEGO STUDY

Comparison Of The Efficacy Bioavailability, Safety Profile And Toxicity Of Artemisinin-Naphtoquinine-Primaquine (ArteGo) And Artemether ¿Lumefantrine In treatment of uncomplicated malaria in Lagos, Nigeria

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201710002665193
Enrollment
120
Registered
2017-10-04
Start date
2017-11-06
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malaria

Interventions

Artemisinine/Naphtoquine/Primaquine
COARTEM GROUP

Sponsors

KINGSGLAIVE CONSULTANTS,
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Clinical symptoms of malaria such as fever etc. age group: above 6 and below 60 years of age, male and female. Plasmodium falciparum asexual forms ¿ 500/¿L observed in peripheral blood smear; Have not been treated with any antimalarial Written informed consent, in accordance with local practice, provided by patient, for children it will provided by either parents or legal representative and in addition children will provide assent. Body weight between 20 kg and 90 kg (both inclusive) Presence of mono-infection with P. falciparum Ability to swallow oral medication Ability and willingness to adhere to all study procedures and access health facilities. Willing to undergo study related procedures including being hospitalized for minimum of 4 nights), and a follow up of up to 28 days.

Exclusion criteria

Exclusion criteria: Age group below 6 or above 60 years Pregnant women Patients with signs and symptoms of severe/complicated malaria as described in the WHO guideline(Third Edition 2012) for management of severe malaria Mixed Plasmodial infection. Severe vomiting, defined as more than three times in the 24 hours prior to inclusion in the study or inability to tolerate oral treatment. Severe diarrhoea defined as 3 or more watery stools per day. Presence of other serious or chronic clinical condition requiring hospitalization. Known history or evidence of clinically significant disorders such as cardiovascular, respiratory (including active tuberculosis), history of jaundice, hepatic, renal, gastrointestinal, immunological, neurological (including auditory), endocrine, infectious, malignancy, psychiatric, history of convulsions or other abnormality (including head trauma). Family history of sudden death or of congenital prolongation of the QT interval or any other clinical condition known to prolong the QT interval.

Design outcomes

Primary

MeasureTime frame
Artemisiine/Naphtoquine/Primauine is effective int the treatment of uncomplicated P. falciparum infection

Countries

Nigeria

Contacts

Public ContactOmoniyi Yemitan
kayodeyemitan@gmail.com08023056011

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026