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CompletedNCT00356005Updated Nov 1, 2012

Azithromycin Combination Therapy for the Treatment of Uncomplicated Falciparum Malaria in Bangladesh

A Phase 2 interventional study of azithromycin plus artesunate and Artesunate in Uncomplicated Falciparum Malaria, sponsored by Medical University of Vienna. Completed at 1 site in Bangladesh. Open to participants aged 8 Years to 65 Years. Per ClinicalTrials.gov, last updated 2012-11-01.

Sponsored by Medical University of Vienna · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
228
Allocation
Randomized
Ages
8 Years to 65 Years
Sex
All
01

Study summary

The purpose of this study is to investigate the efficacy of azithromycin combination therapy with artesunate for the treatment of uncomplicated falciparum malaria in Bangladesh.

Read the detailed description

In view of spreading antimalarial drug resistance there is an urgent need for new combination treatments for a disease that kills more than one million people every year. Azithromycin is a macrolide antibiotic that is particularly attractive due to its safety in children and experience with use in pregnancy. Recent trials suggest that azithromycin has a strong potential as an antimalarial. The purpose of this study is to investigate the efficacy of azithromycin combination therapy for the treatment of uncomplicated falciparum malaria in Bangladesh.

02

Conditions studied

  • Uncomplicated Falciparum Malaria

Keywords

  • falciparum malaria
  • therapy
  • azithromycin
  • artesunate
  • Coartem
  • Bangladesh
03

In context

Malaria

1,299 studies on the registry are indexed under Malaria; 86 are open to participants now.

This study's enrollment of 228 is close to the median of 220 across 1,027 interventional studies indexed under Malaria.

Browse Malaria studies →

Lead sponsor

Medical University of Vienna is the lead sponsor of 1,076 studies on the registry; 177 are open to participants now.

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

04

Who can participate

Ages eligible
8 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Acute symptomatic falciparum malaria infection with a parasite density of 100 to 100,000 asexual parasites/uL as determined on the screening smear with fever (defined as ≥37.5ºC), or reported history of fever within the last 48 hours.
  2. Age: 8-65 years old
  3. Males or females. All females over the age of 12 are required to have a negative human chorionic gonadotropin (hCG) pregnancy test (urine). All females of childbearing potential (not surgically sterile, or less than two years menopausal) are required to use an acceptable method of contraception, such as implant, injectable, oral contraceptive(s) with additional barrier contraception, intrauterine device, sexual abstinence, or vasectomized partner, throughout the study
  4. Written informed consent obtained
  5. Willing to stay under close medical supervision for the study duration
  6. Otherwise healthy outpatients

Exclusion criteria

Exclusion Criteria:

  1. Pregnant women, nursing mothers, or women of childbearing potential who do not use an acceptable method of contraception (as described in Inclusion Criteria, #3)
  2. Mixed malaria infection on admission by malaria smear
  3. A previous history of intolerance or hypersensitivity to the study drugs artesunate, azithromycin, or lumefantrine or to drugs with similar chemical structures
  4. Malaria drug therapy administered in the past 30 days by history
  5. Previous participation in this trial, or participation in any other studies involving investigational or marketed products, concomitantly or within 30 days prior to entry in the study
  6. History of significant cardiovascular, liver or renal functional abnormality or any other clinically significant illness, which in the opinion of the investigator would place them at increased risk.
  7. Symptoms of severe vomiting (no food or inability to take food during the previous 8 hours).
  8. Signs or symptoms of severe malaria (as defined by WHO 2003)
  9. Unable and/or unlikely to comprehend and/or follow the protocol
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
228 participants (actual)

Study arms

  • Experimental
    Azithromycin + Artesunate

    Azithromycin + Artesunate treatment

    Drug: azithromycin plus artesunate

  • Active comparator
    Artesunate

    Artesunate treatment controls

    Drug: Artesunate

Interventions

  • Drugazithromycin plus artesunate
  • DrugArtesunate
06

What researchers measure

Primary outcomes

  1. Primary clinical outcome is cure (ACPR as defined by WHO criteria) on Day 42.

    Time frame: 42 days

Secondary outcomes

  1. Secondary outcome measures are time until parasite, fever, and gametocyte clearance (PCT, FCT, and GCT).

    Time frame: 42

07

Study locations

1 site
  • Sadar Hospital
    Bandarban, Bangladesh
08

References and documents

Publications

  • Thriemer K, Starzengruber P, Khan WA, Haque R, Marma AS, Ley B, Vossen MG, Swoboda P, Akter J, Noedl H. Azithromycin combination therapy for the treatment of uncomplicated falciparum malaria in Bangladesh: an open-label randomized, controlled clinical trial. J Infect Dis. 2010 Aug 15;202(3):392-8. doi: 10.1086/653710. PubMed 20557237 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00356005
Lead sponsor
Medical University of Vienna
Collaborators
International Centre for Diarrhoeal Disease Research, Bangladesh, Armed Forces Research Institute of Medical Sciences, Thailand
Responsible party
Harald Noedl (Assoc. Prof., Medical University of Vienna) — Principal investigator
First posted
Jul 25, 2006
Start date
Aug 2006
Primary completion
Aug 2007
Last update
Nov 1, 2012

Study contacts

Rashidul Haque, MBBS,PhD
principal investigator · International Centre for Diarrhoeal Disease Research, Bangladesh
Harald Noedl, MD, MCTM,PhD
principal investigator · Medical University of Vienna
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.

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