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Clinical Trials in Israel / NCT06885515
Enrolling by invitation Observational

Telomeres Length in Israeli Fibrotic ILD Patients

NCT06885515 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2026-02
Last updated
2026-02-25

Condition(s) studied

Pulmonary Fibrosis

Investigational drug(s) / intervention(s)

leukocyte telomere length (LTL) will be measured using the Telomere Restriction Fragment (TRF) Analysis method

leukocyte telomere length (LTL) will be measured using the Telomere Restriction Fragment (TRF) Analysis method: Peripheral blood leukocytes telomere length will be measured both by TRF analysis and by Nanopore sequencing. Both analyses will be conducted at the laboratory of Prof. Yehuda Tzfati at the Hebrew University, which is highly experienced in the field of telomere biology and in telomere length analysis. Blood samples will be taken once from each participant. No genetic sequencing will be performed as part of this study.

Study summary

Individuals with fibrotic interstitial lung diseases (FILD) will be recruited after providing informed consent. in addition to routine data as usually collected in the clinic, blood samples will be taken for measurement of telomeres length in peripheral blood leukocytes using both the Telomere Restriction Fragment (TRF) Analysis method and Nanopore sequencing. Participants with FILD will be followed-up for 2-year after recruitment, including clinical and pulmonary function tests at-least every 6 months, or more frequently, according to the treating physician discretion.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: 1. Adult subjects, aged ≥18-years-old 2. Able and willing to provide informed consent to participate in the study 3. Lung fibrosis evident on chest CT (signs of honeycombing and/or traction bronchiectasis) \[17\] 4. Subjects fulfilling criteria 1 and 2 but with no evidence of chronic lung disease will serve as controls Exclusion Criteria: 1. Subjects with sarcoidosis as the etiology for FILD 2. Subjects who had undergone lung transplantation 3. Pregnant women

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Barzilai Medical Center Ashkelon Israel
Tel Aviv Medical Center Tel Aviv Israel

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06885515 on ClinicalTrials.gov ↗ ← All trials in Israel