PITT Study: “Cavitary lung lesions and quality of life after TB” Publication (1355)
“Cavitary lung lesions and quality of life after TB” publication for PITT Study.
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Study Type(s)
Topic Area(s)
Document Type(s)
Study Method(s)
Document Method(s)
“Cavitary lung lesions and quality of life after TB” publication for PITT Study.
“High rates of post-tuberculosis lung disease among persons successfully treated for drug-susceptible and resistant tuberculosis” publication for PITT Study.
Pulmonary function test (PFT) series SOP for PITT Study.
Waist circumference measurement SOP for PITT Study.
Blood collection SOP for PITT Study.
Blood collection SOP for PITT Study.
All CRF for PITT Study, includes; Eligibility screening, baseline questionnaire, St. George’s Respiratory Questionnaire for COPD Patients, baseline medical record data collection, baseline pulmonary function test data collection.
COVID Screening & Questionnaire for PITT Study, includes: COVID screening, COVID data collection form, symptoms, and outcomes.
Consent form for PITT Study.
Study Protocol for PITT Study, includes: Abstract, introduction and study rationale, study aims and hypothesis, study design, study measures, study procedures, data management & analysis, protection of human subjects, and references.
PROBeX study retention SOP.
PROBeX handling of sputum samples SOP.
PROBeX blood sample handling for intensive PK sub-study.
PROBeX filing study documents SOP.
PROBeX unscheduled visits SOP.
PROBeX enrollment intensive PK sub-study SOP.
PROBeX screening for participants SOP.
PROBeX international staff monitoring SOP.
PROBeX case report form quality SOP.
PROBeX blood sample processing SOP.
PROBeX transportation and processing sparse PK sampling SOP.
PROBeX initial visit SOP.
PROBeX exit from study SOP.
Follow up visit SOP for PROBeX.
SOP for obtaining medical history PROBeX.
Tracking study progress SOP for PROBeX.
Data management SOP for PROBeX.
Documenting treatment outcomes SOP for PROBeX.
Obtaining informed consent SOP for PROBeX.
Reporting lab assessments SOP for PROBeX.
PROBeX collection, transportation and processing of intensive PK sampling SOP.
Source documentation and participant source file SOP in PROBeX study.
PROBeX monthly follow-up CRF.
Bedaquiline treatment completion CRF in PROBeX study.
PROBeX demographics CRF.
Intensive PK sampling CRF for PROBeX study.
PROBeX HIV medication log CRF.
PK sampling CRF for PROBeX study.
PROBeX TB medication log CRF.
PROBeX participant exit CRF
PROBeX study eligibility from blood results CRF.
Inclusion and exclusion criteria CRF for PROBeX study.
CRF for sputum lab in PROBeX study.
CRF for sputum lab in PROBeX study.
PK sampling follow-up CRF for PROBeX study.
Participant intake history form for PROBeX study.
Protocol for PROBeX study.
PROBeX study participant informed consent form.
PROBeX study participant information sheet.
PROBeX participant screening consent form.