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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02032732
Other study ID # 13-106
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date December 2013
Est. completion date December 2016

Study information

Verified date November 2018
Source University of Tennessee
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pediatric joint infections are a common diagnostic dilemma encountered by treating orthopaedic surgeons. No single test is sensitive or specific enough to stand alone in determining the presence of joint infection.

The purpose of this study is to test the usefulness of a chemical test strip to detect infection in fluid that is removed from a joint (intra-articular aspiration) in pediatric patients. The test strip measures an enzyme called leukocyte esterase, which has been shown to be useful in detecting the presence of infection in fluids from other parts of the body. This study will assess the efficacy of the leukocyte esterase test as a diagnostic tool for evaluating pediatric joint infections. The hypothesis of the study is that a positive leukocyte esterase test identifies a septic joint in pediatric patients undergoing intraoperative joint aspiration.


Description:

Pediatric patients requiring an intra-articular joint aspiration for suspected infection or for other reasons will have a leukocyte esterase test performed on fluid removed from the joint. A convenience sample of consecutive patients will be screened according to inclusion/exclusion criteria and enrolled in the study by informed consent. All patients who will be screened for the study will have already been identified as needing an intra-articular joint aspiration in accordance with standard of care. All patients who are enrolled in the study will have the leukocyte esterase test performed on the fluid that is aspirated. Results of the test strip will be recorded.


Recruitment information / eligibility

Status Terminated
Enrollment 9
Est. completion date December 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 3 Months to 18 Years
Eligibility Inclusion Criteria:

- All patients at this facility over the age of 3 months and below the age of 18 years who receive an intra-articular aspiration

Exclusion Criteria:

- Immunocompromised patients

- Renal failure patients

- Patients younger than 3 months old

- Patients 18 years of age or older

- Volume of aspirate is less than 1.5 mL

Study Design


Intervention

Other:
leukocyte esterase test
leukocyte esterase test on fluid removed by intra-articular aspiration

Locations

Country Name City State
United States Children's Orthopaedics, Erlanger Health System Chattanooga Tennessee

Sponsors (1)

Lead Sponsor Collaborator
University of Tennessee

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary leukocyte esterase level using a leukocyte esterase test strip A positive leukocyte esterase test strip will be considered an indicator of a septic joint at the time of an intraoperative joint aspiration
Secondary baseline leukocyte esterase level for pediatric patients using a leukocyte esterase test strip at the time of intraoperative joint aspiration
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