Viewing Study NCT00172783



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00172783
Status: UNKNOWN
Last Update Posted: 2005-09-15
First Post: 2005-09-12

Brief Title: PPD Size and Mycobacteria Tuberculosis ELISPOT in Children Who Have Received BCG in Neonate Period
Sponsor: National Taiwan University Hospital
Organization: National Taiwan University Hospital

Study Overview

Official Title: PPD Size and Mycobacteria Tuberculosis ELISPOT in Children Who Have Received BCG in Neonate Period
Status: UNKNOWN
Status Verified Date: 2005-06
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To investigate the size of PPD and TB specific ELISPOT among children between 3mo and 15 yo Calculate the normal range of age specific PPD size in children who recieved BCG at new-born period
Detailed Description: Sampling

1 Age under 3 year-old a targeted population contains 500 children will be used for sampling of this group This cohort were firstly enrolled for a trial of oral Rota vaccine since 2004 They will be followed up in the cohort up to 2006 Sixty children will be enrolled in the group younger than 1 year-old 1-2 2-3 year-old 20 children will be enrolled in each age group
2 Age of 3 to 5 year-old cases will be enrolled from volunteered students from kindergarden 3-4 4-5 5-6 year-old 20 children will be enrolled in each age group
3 Age of 6 to 15 year-old cases will be enrolled from volunteered students from elementary school and junior high school 30 children will be enrolled in each age group A total of 300 children will be enrolled from children between 6 year-old and 15 year-old

3 A total of 460 children between the age of 3 month and 15 yo will be enrolled

Procedure of PPD test Children who fit the criteria will be given 01 ml of PPD PPD RT23 2 units intradermally in accordance with the guidelines recommended by WHO 17 The tuberculin for the tests is obtained from Denmark and is used throughout the country PPD indurations will be read 48 to 72 h after administration at 90 degrees from the longest axis of the arm and recorded to the nearest millimeter Indurations 5 mm in diameter are classified as negative those 5 but 10 mm as doubtful and those 10 mm as positive according to previous consensus 2 All size of indurations will be recorded for further analysis other than arbiturary classification

Procedure of ELISPOT assay to detect T cells specific for M tuberculosis antigens 4 ml whole blood is collected in a heparinized tube first and are processed and scored by two scientists who had no access to personal identifiers or TST results within four hours after collection We amplified the esat-6 gene from genomic DNA isolated from M bovis strain AN5 by PCR and cloned it into plasmid vector pET21d Novagen Madison WI USA Escherichia coli was transformed with this vector Recombinant ESAT-6 was recovered from transformed E coli and purified by nickel-affinity chromatography We did ex-vivo interferon-gamma ELISPOT assays with 300 000 peripheral blood mononuclear cells per well 1418 We used purified recombinant ESAT-6 and PPD in addition to negative controls no added antigen and positive controls phytohaemagglutinin Positive ESAT-6 test wells were defined as containing at least ten spot-forming cells more than and at least twice as many as negative control wells-a detection threshold of one per 30 000 peripheral blood mononuclear cells Assays were done and independently scored by two scientists who were unaware of exposure category and TST results of contacts ELISPOT assay wells containing more than 300 spot-forming cells cannot be counted accurately because the spots coalesce 300 cells per well equivalent to 1000 cells per million peripheral blood mononuclear cells was therefore taken as the upper limit for accuracy 15

Exclusion and Follow-up steps Children who are found to have positive PPD test 10 mm have a PPD size in the range of 1st 25 percentile or having a positive ELISPOT result at the time of enrollment will be closely followed up for clinical symptoms and signs of TB and necessary diagnostic workup will be done If LTBI is highly suspected prophylaxis will be initiated Closed contact families and care-givers will be asked to take CXR for excluding active pulmonary TB

Information collection at the enrollment Cross-sectional study of 160 children will be conducted Children were examined and assessed for general health condition BCG vaccination record and BCG scar over Lt arm 19 Possible TB exposure including elderly with chronic cough or unexplained prolonged febrile illness in house-hold contact any contact history with documented open TB will be thoroughly evaluated Children with suspicious immuno-compromised status active lung disease or exposure history of TB will be excluded and follow-up will be done

Biostatistic method Descriptive analysis will be used for size of PPD and result of ELISPOT P value is calculated with student t test or Chi-square or Fisher exact test for statistic significance Version 100 SPSS SPSS Inc Illinois between different age group 95CI will be calculated for the purpose of cut off value of PPD size except those with unexpected-found TB disease

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None