ClinicalTrials.Veeva

Menu

Nutritional Assessment in Non-tuberculous Mycobacteria Pulmonary Disease (nutriNTM)

U

University of Milano Bicocca

Status

Enrolling

Conditions

Non-Tuberculous Mycobacterial Pneumonia

Study type

Observational

Funder types

Other

Identifiers

NCT05376280
nutriNTM

Details and patient eligibility

About

Non-tuberculous mycobacterial (NTM) pulmonary disease (PD) is an emerging condition with heterogeneous manifestations from both the microbiological and the clinical point of view. Diagnostic and therapeutic guidelines are available but there are still unmet patients' and physicians' needs, including the exams to perform in the nutritional evaluation and intervention to improve health-related QoL and to control gastrointestinal side-effects during antimicrobial therapy, particularly in those with low body mass index and history of weight loss.

Full description

The aim of the study is to evaluate the nutritional status in patients with non-tuberculous mycobacterial pulmonary disease (NTM-PD) and to provide an initial assessment of the potential impact of the introduction of targeted antibiotic therapy on the nutritional status itself.

Specifically, the primary objective is the assessment of the proportion of underweight subjects, i.e. with Body Mass Index (BMI) <18.5 kg/m2, to confirm that it is significantly higher than that of the general Italian population.

Study Design: Multicenter Cohort Pilot Observational Study

Participation in the study consists of two pneumological visits, as per normal clinical practice, (at the beginning of the study, T1, after 6 months, T3, and at the end of the antimicobacterial antibiotic therapy, T5) in which the collection of past medical history, measurement of oxygen saturation, pulmonary functional tests and 6-minute walking tests will be performed. In addition, nutritional assessments (T2, T4, T6) will be carried out at the same time as the pulmonary visits. Nutritional assessments will include anthropometric measurements, questionnaires on nutritional status and physical activity, performing blood chemistry tests, bioimpedance, dynamometry and gait speed 4 meters, to evaluate body composition and physical performance.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age greater than or equal to 18 years;
  • diagnosis of NTM-PD according to the BTS 2017 guidelines

Exclusion criteria

  • severe renal failure, defined as a GFR (glomerular filtration rate) lower than 30ml / min; NYHA class IV;
  • severe liver failure, defined as Child-Pugh score class C;
  • active solid or haematological neoplasms;
  • having already received (currently or in the prior 6 months) antimicobacterial therapy;
  • severe immunosuppression;
  • inability to walk without help;
  • need for oxygen therapy at rest;
  • participation in other interventional experimental protocols with use of a medicinal product.

Trial contacts and locations

1

Loading...

Central trial contact

Paola Faverio, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems