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Prospective Analysis of Urine LAM to Eliminate NTM Sputum Screening

Prospective Analysis of Urine LAM to Eliminate NTM Sputum Screening (PAINLESS Trial)

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04579211
Acronym
PAINLESS
Enrollment
220
Registered
2020-10-08
Start date
2020-12-10
Completion date
2026-05-01
Last updated
2025-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Brief summary

This is a prospective, single-center, nonrandomized observational study to investigate the utility of urine lipoarabinomannan (LAM) as a test to identify individuals at very low risk for having a sputum culture positive for Nontuberculous Mycobacteria (NTM). The study is designed to evaluate if a urine test can eliminate the need for obtaining a sputum specimen to screen for NTM in individuals with Cystic Fibrosis (CF). The participants will be asked to provide 3 urine samples either in person or by mail over approximately 3 years. The 3 urine sample requests will be timed to coincide with their usual clinical care and routine sputum collection.

Interventions

DIAGNOSTIC_TESTurine lipoarabinomannan (LAM)

Investigate the utility of urine LAM as a test to identify individuals at very low risk for having a sputum culture positive for NTM.

Sponsors

Jerry A. Nick, M.D.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Informed consent obtained online or in person from the participant * Enrolled in the CFF Patient Registry (CFFPR) * Be willing and able to adhere to study procedures in the context of clinical care, and other protocol requirements * Diagnosis of CF consistent with the 2017 CFF Guidelines NTM culture status of negative (defined by a review of clinical and culture data with at least 3 years of clinical data available to review and at least one negative culture within the year prior to enrollment and no known history of previous positive cultures for pathogenic NTM)

Exclusion criteria

1\. Has any other condition that, in the opinion of the Site Investigator/designee, would preclude informed consent or assent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives

Design outcomes

Primary

MeasureTime frameDescription
To determine the ability of the urine LAM assay to predict continued negative sputum culture over the next 12 months.From time enrollment to over the next 12 monthsCorrelation of a negative NTM sputum culture in the year following a negative urine LAM assay

Secondary

MeasureTime frameDescription
To determine the ability of the urine LAM assay to predict new positive NTM sputum culture over the next 12 months.From time of enrollment to over the next 12 monthsCorrelation of a positive NTM sputum culture in the year following a positive urine LAM assay
To determine the time between a positive LAM assay and a new positive NTM culture.3 yearsCorrelation of a positive NTM sputum culture up to 3 years following a positive urine LAM assay
To facilitate the development of a ELISA-based assay as a possible replacement to GC/MS in the clinical setting.3 yearsExcess urine will be used to develop and validate an alternative assay using ELISA.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026