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CompletedNCT01722539PIP-IPTUpdated Feb 4, 2014

Impact IPT With Sulfadoxine-pyrimethamine or Sulfadoxine-pyrimethamine Plus Piperaquine in Schoolchildren

A Phase 3 interventional study of Sulfadoxine-pyrimethamine and Piperaquine in Healthy, sponsored by Universiteit Antwerpen. Completed at 1 site in Congo. Open to participants aged 5 Years to 14 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-02-04.

Sponsored by Universiteit Antwerpen · Phase 3, Interventional, and Prevention

Phase
Phase 3
Study type
Interventional
Enrollment
616
Allocation
Randomized
Ages
5 Years to 14 Years
Sex
All
01

Study summary

Considering the facts that: (i) IPT of malaria provides substantial protection against anaemia and malaria in school children (ii); SP resistance has no significant impact on the prophylactic efficacy (iii) SP-PQ is safe and as efficacious as SP: the investigators hypothesize that antimalarial IPT with SP and SP-PQ will improve haemoglobin concentration, reduce anaemia prevalence, malaria incidence and parasitaemia, and improve malnutrition and school performance in school-aged children of Congo.

Read the detailed description

STUDY RATIONAL The education sector represents a reliable system for malaria control. Intermittent preventive therapy in schoolchildren (IPTsc) is likely the most feasible and appropriate chemoprevention in stable and endemic areas because schoolchildren are usually asymptomatic to malaria infection and are consequently untreated in practice. Therefore, if proven effective, IPTsc would be of direct benefit for the schoolchild, contribute to malaria control at school, and facilitate community-wide the implementation of other control interventions i.e. vector control, Intermittent preventive therapy in infants (IPTi), and prompt diagnosis and treatment (PDT). Nevertheless, evidence about use of IPTsc is not yet substantiated as only two clinical studies have so far been performed on IPTsc in hyper endemic areas. Further clinical trials are warranted in other settings. Through a randomised controlled trial (RCT) we will assess the efficacy and safety, of two IPT regimens versus controls in school children of the DRCongo.

STUDY DRUGS Favourable drugs for use as IPT should balance long half-life against efficacy, safety, tolerability and potentiality for cross-resistance selection.(16) Use of long-acting drugs would result in fewer intake and higher treatment compliance. Sulfadoxine-pyrimethamine is an established used product in the indication of IPT in pregnancy. The drug has further proven safety and tolerability in children in clinical trials. SP is slowly eliminated and allows 60 days antimalaria protection for fully sensitive P. falciparum. Other long-acting drugs available are mefloquine, amodiaquine, and piperaquine. However, due safety concern mefloquine might not be optimal for IPT. Amodiaquine is not suitable for IPT due to its 3 days treatment regimen that may be a concern regarding compliance. Piperaquine has been extensively used for mass prophylaxis and treatment since 1978 in China and other malaria endemic countries of Asia.(20) Piperaquine has a long half-live and points as good IPT candidate in endemic country with SP resistance. For this study sulfadoxine-pyrimethamine combined with piperaquine (SP-PQ) plus will be used. SP and SP-PQ will be given at 4 months intervals in line with the long half-lives (around 20 days) in paediatric patients and for higher treatment compliance,

02

Conditions studied

  • Healthy

Keywords

  • intermittent
  • preventive
  • treatment
  • malaria
  • soil transmitted helminths
  • schistosomiasis
  • schoolchildren
03

In context

Malaria

1,184 studies on the registry are indexed under Malaria; 79 are open to participants now.

This study's enrollment of 616 is above the median of 252 across 937 interventional studies indexed under Malaria.

Browse Malaria studies →

Lead sponsor

Universiteit Antwerpen is the lead sponsor of 135 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 14 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • males and females in primary school children,
  • anticipated local residence for the study duration,
  • signed or thumb-printed by the parents or guardians and witnessed by an impartial witness (whenever parents/guardians are illiterate)

Exclusion criteria

Exclusion Criteria:

  • Children of the 6th primary school year
  • Participation in any other drug study (antimalarial or others) during the previous 30 days.
  • Known or serious adverse drug reaction (ADR) to the study drugs.
  • Clinical malaria at baseline irrespectively of the severity (World Health Organisation malaria treatment guideline 2010) (Annex III).
  • Febrile conditions caused by diseases other than malaria at first visit.
  • Clinical symptoms of severe anaemia
  • Illness or conditions like hematologic, cardiac, renal, hepatic diseases which in the judgement of the investigator would place the subject at undue risk or interfere with the results of the study, including known Glucose 6 phospahate dehydrogenase (G6PD) deficiency and sickle cell (SS form).
  • Body weight \< 14 kg Children with major chronic infectious diseases (, Tuberculosis, ...)
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

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Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
616 participants (actual)

Study arms

  • Experimental
    Sulfadoxine-Pyrimethamine

    Sulfadoxine-Pyrimethamine every Four months Tablets 500 mg sulfadoxine - 25 mg pyrimethamine will be given as single oral dose of ½ tablets per 10 kg of weigh: 1 tablet for weigh less than 20 kg, 1.5 tablets in 20-29 kg, and 2 tablets for children of weigh 30 or more; Albendazole oral 200 mg will be given to children of 1-2 years and one oral dose of 400 mg to children older than 2 years. The treatment will be repeated at 4-months in the follow-up in accordance with the WHO guideline. Praziquantel is a tremacide used for treatment of infections due to schistosomes. Praziquantel will be given as one dose of 40 mg/kg at enrolment and at 12 months follow up.

    Drug: Sulfadoxine-pyrimethamine · Drug: Piperaquine · Drug: Albendazole · Drug: Praziquantel

  • Experimental
    Sulfadoxine-Pyrimethamine+Piperaquine

    Sulfadoxine-Pyrimethamine every 4 months Tablets 500 mg sulfadoxine - 25 mg pyrimethamine will be given as single oral dose of ½ tablets per 10 kg of weigh: 1 tablet for weigh less than 20 kg, 1.5 tablets in 20-29 kg, and 2 tablets for children of weigh 30 or more; Piperaquine every four months Piperaquine tablet 320 mg manufactured by Sigma Tau will be used at two treatment doses of 16-24 mg/kg at 24 hours intervals as follows: 1 tablets for weigh 15-19 kg, 1.5 tablets for 20-29 kg, and 2 tablets for 30-39 kg, and 2.5 tablets for 40 kg or more. Albendazole oral 200 mg will be given to children of 1-2 years and one oral dose of 400 mg to children older than 2 years. The treatment will be repeated at 4-months in the follow-up in accordance with the WHO guideline. Praziquantel is a tremacide used for treatment of infections due to schistosomes. Praziquantel will be given as one dose of 40 mg/kg at enrolment and at 12 months follow up.

    Drug: Piperaquine · Drug: Albendazole · Drug: Praziquantel

  • Active comparator
    Control

    Albendazole oral 200 mg will be given to children of 1-2 years and one oral dose of 400 mg to children older than 2 years. The treatment will be repeated at 4-months in the follow-up in accordance with the WHO guideline. Praziquantel is a tremacide used for treatment of infections due to schistosomes. Praziquantel will be given as one dose of 40 mg/kg at enrolment and at 12 months follow up.

    Drug: Albendazole · Drug: Praziquantel

Interventions

  • DrugSulfadoxine-pyrimethamine

    Tablets 500 mg sulfadoxine - 25 mg pyrimethamine will be given as single oral dose of ½ tablets per 10 kg of weigh: 1 tablet for weigh less than 20 kg, 1.5 tablets in 20-29 kg, and 2 tablets for children of weigh 30 or more

    Also known as: Fansidar

  • Piperaquine tablet 320 mg manufactured by Sigma Tau will be used at two treatment doses of 16-24 mg/kg at 24 hours intervals as follows: 1 tablets for weigh 15-19 kg, 1.5 tablets for 20-29 kg, and 2 tablets for 30-39 kg, and 2.5 tablets for 40 kg or more.

  • One oral 200 mg will be given to children of 1-2 years and one oral dose of 400 mg to children older than 2 years. The treatment will be repeated at 4-months in the follow-up in accordance with the WHO guideline.

  • Praziquantel is a tremacide used for treatment of infections due to schistosomes. Praziquantel will be given as one dose of 40 mg/kg at enrolment and at 12 months follow up.

06

What researchers measure

Primary outcomes

  1. Hemoglobin change

    Change in mean Hb concentration at month 12 of follow-up and anaemia prevalence one year after initial preventive treatment;

    Time frame: Month 0-Month 12

Secondary outcomes

  1. Change in mean Hb concentration at month 4 and 8 of follow-up

    Time frame: Month 0 - Month 4 - Month 8

  2. Prevalence of asymptomatic and clinical malaria at baseline & one year after enrolment;

    Time frame: Month 0 Month 12

  3. Prevalence of P. falciparum dihydrofolate reductase (dhfr) and dihydropteroate synthase (dhps) gene mutations at baseline and at month 12 follow-up

    Time frame: Month 0 - Month 12

  4. Clinical (severe) malaria incidence and parasitaemia at month 4, 8, 12;

    Time frame: Month 4, 8 12

  5. Percentages of acute and severe malnourished at month 0, 4, 8, 12 through z-scores, W/H, H/A, and skinfolds

    Time frame: Month 0 - Month 12

  6. Educational achievement, at end of follow-up, and school attendance;

    Time frame: Month 0 - Month 12

  7. Prevalence and risk of environmental and host-related predictors for malaria (re)infections;

    Time frame: Month 0- Month 12

  8. adverse events

    Time frame: Month 0- Months 12

07

Study locations

1 site
  • Mokali health area of Biyela health zone, in Kinshasa province.
    Kinshasa, Kinshasa province, Congo
08

References and documents

Publications

  • Doua JY, Matangila J, Lutumba P, Van Geertruyden JP. Intermittent preventive treatment: efficacy and safety of sulfadoxine-pyrimethamine and sulfadoxine-pyrimethamine plus piperaquine regimens in schoolchildren of the Democratic Republic of Congo: a study protocol for a randomized controlled trial. Trials. 2013 Sep 24;14:311. doi: 10.1186/1745-6215-14-311. PubMed 24063608 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01722539
Collaborators
Fund for Scientific Research, Flanders, Belgium, University of Kinshasa
Responsible party
Jean-Pierre Van geertruyden (Prof, Universiteit Antwerpen) — Principal investigator
First posted
Nov 7, 2012
Start date
Nov 2012
Primary completion
Nov 2013
Completion
Nov 2013
Last update
Feb 4, 2014

Study contacts

Junior Matangila, MD
principal investigator · University of Kinshasa
Pascal Lutumba, MD PhD
study director · University of Kinshasa
Joachim Doua, MD
principal investigator · Universiteit Antwerpen

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Piperaquine

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