A Pilot Study to Assess Body Mass Composition Measurement Using BIA and Muscle Ultrasound in IPF and PPF Patients on Anti-fibrotic Medications

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRoyal Brompton & Harefield NHS Foundation Trust

About this trial

To assess the impact on body mass composition from anti-fibrotic medications used in fibrotic lung disease by using BIA and muscle ultrasound

Eligibility criteria

Qualifiers

A diagnosis of Idiopathic pulmonary fibrosis or progressive pulmonary fibrosis

Newly commencing anti-fibrotic medication (either nintedanib or pirfenidone)

Subject aged > 18 years

Able to willingly give consent

Disqualifiers

Co-morbidities currently requiring enteral feeding

Weight loss > 10% in preceding 3-6 months

Significant musculoskeletal issues that may impact muscle mass

End of life care (expected < 6 weeks left to live)

Trial design

Treatments tested in this trial

  • No Interventions
  • No intervention

Treatment groups

30 Participants
are divided into 2 treatment groups