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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01094431
Other study ID # Fever 2010
Secondary ID
Status Completed
Phase N/A
First received March 26, 2010
Last updated December 2, 2014
Start date April 2011
Est. completion date July 2011

Study information

Verified date December 2014
Source Karolinska University Hospital
Contact n/a
Is FDA regulated No
Health authority Regional Ethical Committee, Stockholm, Sweden:MOH Research Council, Zanzibar, Tanzania:
Study type Observational

Clinical Trial Summary

The purpose of this study is to study the most common etiologies of uncomplicated fever diseases among children under five years of age in rural Zanzibar.


Description:

During the last 6 years Zanzibar has undergone a dramatic change in malaria epidemiology and burden of disease, with a marked decline of Plasmodium falciparum malaria among febrile children from approximately 30% to 1% or below and a reduction of crude child mortality of 50%. Millions of children in Africa die of neonatal disorders, acute respiratory tract infections (ARI), diarrhea, malaria, measles, HIV and malnutrition. A majority of these illnesses are also a common cause of febrile illness in out-patient departments. However, most of the few fever studies made in Africa are hospital based Very few studies on etiology of childhood febrile disease have been conducted on first level health facilities in the least developed countries in Africa. This study will therefore focus on children between 2 months to 5 years of age that have been diagnosed with a negative rapid diagnostic test (RDT) for malaria and their causes of fever at the first referral level in out-patient clinics in Zanzibar.


Recruitment information / eligibility

Status Completed
Enrollment 690
Est. completion date July 2011
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Both
Age group 2 Months to 59 Months
Eligibility Inclusion Criteria:

- Patients between 2-59 months of age with confirmed fever, with a measured axillary temperature of =37.5°C, or history of fever within the preceding 24 hours.

- Presenting at the health facility from 8.00 to 16.00 Monday to Friday.

- Informed consent.

- Able and willing to complete stipulated follow-up.

Exclusion Criteria:

- Decision by the clinician to refer the patient to another health facility than the PHCC where the study is conducted.

- Symptoms/ signs of severe disease that requires immediate referral from the PHCC as defined by the clinicians. These symptoms/signs of severe disease are according to the IMCI guidelines.

Study Design

Observational Model: Cohort


Related Conditions & MeSH terms


Locations

Country Name City State
Tanzania Facility: Primary health care center (PHCC), Kivunge, North A district, Zanzibar Kivunge Zanzibar

Sponsors (5)

Lead Sponsor Collaborator
Karolinska University Hospital Göteborg University, Queen Silvia Children's Hospital, Gothenburg,. Sweden, World Health Organization, Zanzibar Malaria Control Programme

Country where clinical trial is conducted

Tanzania, 

Outcome

Type Measure Description Time frame Safety issue
Primary relative frequency of febrile diseases etiology Five months No
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