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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02700269
Other study ID # MRT15003.2
Secondary ID 5D43TW009348
Status Completed
Phase
First received
Last updated
Start date April 2016
Est. completion date February 2019

Study information

Verified date February 2020
Source Macha Research Trust, Zambia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Investigators will evaluate approaches using magnetic bead capture, isolation, and surface tension valve transfer of biomarkers to process capillary blood in order to improve the sensitivity of already approved Rapid Diagnostic Tests (RDTs) for detection of human malaria infection. Results will be compared to those obtained using unenhanced capillary blood specimens directly applied to approved malaria RDTs. Participants seeking care for possible malaria in Zambia will be recruited to enroll in the study.


Other known NCT identifiers
  • NCT02698774

Recruitment information / eligibility

Status Completed
Enrollment 278
Est. completion date February 2019
Est. primary completion date February 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Months to 85 Years
Eligibility Inclusion Criteria:

- Individuals giving written informed consent for themselves

- Children under the age of 18 for whom a parent or guardian can give consent

- Individuals seeking care or treatment of suspected or possible malaria

- Individuals being screened as a contact of someone with recent malaria

- Other individuals willing to have their blood tested for malaria

Exclusion Criteria:

- Anyone over 18 unwilling or unable to provide informed consent

- Anyone under 18 who does not have a parent or guardian to give consent

- Anyone between the age of 12 and 18 who does not give assent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
mBEADS
Evaluate approaches using magnetic bead capture, isolation, and surface tension valve transfer of biomarkers to improve the sensitivity of already approved malaria RDTs.

Locations

Country Name City State
Zambia Macha Research Trust Choma

Sponsors (4)

Lead Sponsor Collaborator
Macha Research Trust, Zambia John E. Fogarty International Center (FIC), National Institutes of Health (NIH), Vanderbilt University

Country where clinical trial is conducted

Zambia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Enhancement of malaria RDT to detect low levels of P falciparum parasites The expected outcome of this research project is to enhance the ability of standard malaria RDTs to detect low levels of Plasmodium falciparum malaria in human capillary blood. 5 years
See also
  Status Clinical Trial Phase
Recruiting NCT03511443 - Evaluation of the Performance of a hsRDT Versus cRDT in Reactive Case Detection of Malaria Infections N/A
Completed NCT02371395 - Validation of RealAmp Method for the Diagnosis of Malaria in Endemic Areas of Brazil
Completed NCT04147546 - Additional Screening With Sensitives RDTs and Malaria Phase 3