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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03648411
Other study ID # DMR_2018-108
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 12, 2019
Est. completion date May 20, 2020

Study information

Verified date July 2020
Source Department of Medical Research, Lower Myanmar
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A cross-sectional study will be conducted in selected 2 sentinel sites for assessment of drug resistance falciparum and vivax among asymptomatic infection in migrant workers in Myanmar.


Description:

Although malaria prevalence is decreasing in Myanmar, drug resistance threatens the malaria elimination by 2030 especially high risk persons including migrant population. Previous study indicated that asymptomatic malaria parasite carried drug resistance gene such as K13 mutant that is genetically responsible for artemisinin resistant falciparum malaria. These asymptomatic carries may be a source to spread the disease and it is very important to conduct the surveillance on drug resistance status among high vulnerable persons. Unfortunately, there is no study to assess the drug resistance molecular markers in asymptomatic malaria among migrant workers in Myanmar. Therefore, this study fulfills the gaps of knowledge on important of asymptomatic hidden infection exploring to formulate the recommendation for elimination of malaria in Myanmar.

In this study, asymptomatic infections are screened by rapid diagnostic test, microscopy and molecular methods.


Recruitment information / eligibility

Status Completed
Enrollment 765
Est. completion date May 20, 2020
Est. primary completion date December 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age above 6 year

- Migrant population (moving from their normal residence place and working at a new place such as forest related activities, gold-mines or plantation sites for more than 3 months- 3 years)

- Both sex

- Participant who give informed-consent to participate the study

Exclusion Criteria:

- Known clinical malaria cases regardless of the species detected

- Patients with clinical symptoms of malaria at the time of examination

- Known history of malaria within 14 days

Study Design


Intervention

Genetic:
Drug resistance molecular markers
Proportion of the drug resistance molecular markers will be found-out and compared.

Locations

Country Name City State
Myanmar Dr. Myat Phone Kyaw Yangon

Sponsors (2)

Lead Sponsor Collaborator
Department of Medical Research, Lower Myanmar National Malaria Control Program, Myanmar

Country where clinical trial is conducted

Myanmar, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of the asymptomatic infection among the study population Number of the hidden malaria cases by RDT, microscopy or nested PCR (molecular method) 1 week
Primary Proportion of the drug resistance molecular markers among asymptomatic infections Among the asymptomatic cases, molecular markers will be analyzed (K13 and pfmdr1 copy number for falciparum and pvcrt-o, pvmdr1, pvdhps and pvdhfr gene analysis for vivax cases by Sanger Sequencing. 3 months
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