NCT03847870

Brief Summary

Rickettsial infections have been found to be the second most common cause of non-malarial febrile illness in Southeast Asia, just after dengue, and are largely neglected treatable causes of morbidity and mortality. The rickettsiae can be divided into three major groups: the scrub typhus group (STG), the typhus group (TG) and the spotted fever group (SFG). Rickettsial infections typically present with an acute fever and are difficult to diagnose due to the many different causes of undifferentiated fever in Southeast Asia. Rickettsial IgG seroprevalence, reflecting past infection, will give an estimate of the burden of rickettsial infections in the population. Background seroprevalence studies in countries around Myanmar have found high rates of rickettsial infections. Yet, in Myanmar there have been no prevalence studies on rickettsial infections since the Second World War. We plan to determine IgG levels to the three different groups of rickettsial infections in leftover blood samples in several clinics and hospitals in different regions of Myanmar.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
700

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 19, 2019

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 20, 2019

Completed
4 months until next milestone

Study Start

First participant enrolled

June 20, 2019

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 25, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 25, 2019

Completed
Last Updated

January 13, 2020

Status Verified

January 1, 2020

Enrollment Period

4 months

First QC Date

February 19, 2019

Last Update Submit

January 9, 2020

Conditions

Keywords

rickettsiaeseroprevalence

Outcome Measures

Primary Outcomes (1)

  • Positive ELISA confirmed by positive IFA

    Proportion of patients with a positive IgG ELISA, subsequently confirmed with IFA, for scrub typhus (Orientia tsutsugamushi strains Karp, Kato, Gilliam and TA716), murine typhus (Rickettsia typhi strain type Wilmington), and spotted fever rickettsiosis (Rickettsia honei and Ricketsia conorii).

    January, 2020

Secondary Outcomes (1)

  • Patient characteristics associated with rickettsial infections

    January, 2020

Interventions

An in-house rickettsial IgG ELISA test will be used for this study to determine previous rickettsial infections by measuring IgG levels. All specimens will be tested for IgG antibodies using ELISA tests for scrub typhus (Orientia tsutsugamushi strains Karp, Kato, Gilliam and TA716), murine typhus (Rickettsia typhi strain type Wilmington), and spotted fever rickettsiosis (Rickettsia honei and Rickettsia conorii). If the sample tests positive, it will be retested for the same antigens using the IFA test. The sample will be considered positive if both the ELISA and the IFA are positive.

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The population investigated will be patients who had a leftover samples from routine clinical blood draw when attending seven different Medical Action Myanmar (MAM) clinics and hospitals in different regions of Myanmar with each site including approximately 100 patients.

You may qualify if:

  • Male and female, all age groups, requiring a blood draw for a routine clinical purpose

You may not qualify if:

  • Leftover blood sample of less than 500μL

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Myanmar Oxford Clinical Research Unit

Yangon, Burma

Location

Related Publications (27)

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Study Officials

  • Elizabeth Anne Ashley, Dr

    Myanmar Oxford Clinical Research Unit

    PRINCIPAL INVESTIGATOR
  • Stuart Blacksell, Prof

    Mahidol Oxford Tropical Medicine Research Unit

    PRINCIPAL INVESTIGATOR
  • Philip Elders, MSc

    Myanmar Oxford Clinical Research Unit

    STUDY DIRECTOR
  • Wei Yan Aung Htay, Dr

    Myanmar Oxford Clinical Research Unit

    STUDY DIRECTOR
  • Yin Yin Htwe, Dr

    National Health Laboratory, Myanmar

    STUDY DIRECTOR
  • Myat Myat Moe, Dr

    Magway General Hospital, Magway

    STUDY DIRECTOR
  • Wai Mon Kyaw, Dr

    Monywa Hospital, Sagaing

    STUDY DIRECTOR
  • Ni Ni Zaw, Dr

    Mandalay General Hospital and University of Medicine, Mandalay

    STUDY DIRECTOR
  • Win May Thein, Prof

    Mandalay General Hospital and University of Medicine, Mandalay

    STUDY DIRECTOR
  • Thin Thin Nwe, Prof

    University of Medicine, Magway

    STUDY DIRECTOR
  • Kyaw Soe, BSc

    Myanmar Oxford Clinical Research Unit

    STUDY DIRECTOR
  • Ampai Tanganuchitcharnchai, BSc

    Mahidol Oxford Tropical Medicine Research Unit

    STUDY DIRECTOR
  • Ni Ni Tun, Dr

    Myanmar Oxford Clinical Research Unit and Medical Action Myanmar

    STUDY DIRECTOR
  • Frank Smithuis, Prof

    Myanmar Oxford Clinical Research Unit and Medical Action Myanmar

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 19, 2019

First Posted

February 20, 2019

Study Start

June 20, 2019

Primary Completion

October 25, 2019

Study Completion

October 25, 2019

Last Updated

January 13, 2020

Record last verified: 2020-01

Locations