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Idiopathic Pulmonary FibrosisNCT03258801

Pirfenidone as Bridging Therapy for Lung Transplant in Patients Suffering From Idiopathic Pulmonary Fibrosis

An observational study of Idiopathic Pulmonary Fibrosis and Lung Transplant; Complications, run by Dr. Christopher Lambers at 1 site in Austria.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

The diagnosis of idiopathic pulmonary fibrosis (IPF) is currently one of the most common diagnoses for patients under evaluation for lung transplantation. In recent years, an absolute increase in prevalence/ incidence of IPF has been observed. Read more about this study

Who is it for?
Ages 40 to 70 years
How many people
0 participants
Where
1 siteAustria
Study dates
29 Oct 2018to 2 Dec 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: All patients who are admitted to the lung transplantation department and fulfill the international criteria for idiopathic pulmonary fibrosis will be evaluated (existence of a usual interstitial pneumonia (UIP) pattern in the high-resolution computed tomography (HRCT) is necessary). The assignment of a patient to a particular therapeutic strategy remains in the sole responsibility of the treating physician and must not be dictated by this study-specific observation- and evaluation plan

Who may be able to join

  • For Pirfenidone Group
  • Patients must meet all of the following inclusion criteria to be eligible for inclusion in the study
  • mild to moderate idiopathic pulmonary fibrosis (IPF).
  • Current or intended treatment with Pirfenidone
  • Diagnosis of Interstitial Lung disease
  • Evaluation for Lung Transplantation
Show all 13Show fewer
  • Age 40-70
  • For Control Group
  • Patients must meet all of the following inclusion criteria to be eligible for inclusion in the study
  • mild to moderate idiopathic pulmonary fibrosis (IPF).
  • Diagnosis of Interstitial Lung disease
  • Evaluation for Lung Transplantation
  • Age 40-70

Who cannot join

  • For Pirfenidone Group
  • Other lung diseases (such as cystic fibrosis, COPD)
  • Infection with Hepatitis C,
  • Liver cirrhosis CHILD C
  • Coronary heart disease (3VD)
  • For Control Group
Show all 10Show fewer
  • Other lung diseases (such as cystic fibrosis, COPD)
  • Infection with Hepatitis C,
  • Liver cirrhosis CHILD C
  • Coronary heart disease (3VD)

Trial locations and contacts

1 site in 1 country.

Austria1 site
  • Medical University of Vienna, Department of Surgery

    Vienna, 1090

Other trials in Austria

About this study

The diagnosis of idiopathic pulmonary fibrosis (IPF) is currently one of the most common diagnoses for patients under evaluation for lung transplantation. In recent years, an absolute increase in prevalence/ incidence of IPF has been observed. There is evidence that patients with IPF on waiting list for lung transplantation might benefit from pirfenidone treatment. Until now, no data are published regarding this important issue in lung transplantation.

Primary objective is to determine whether there is a difference in the duration time of mechanical ventilation (weaning) directly after lung transplantation between patients treated with pirfenidone and patients without pirfenidone treatment. The Secondary objectives are to determine whether there are differences between the pirfenidone treatment group and the control group regarding survival after LUTX, the score on the Saint Georges Respiratory Questionnaire and the decline in forced vital capacity (FVC%) In this Investigator initiated, non- interventional single center study , patients on the waiting list for transplant pirfenidone treatment receive oral pirfenidone at the standard dose of 2403 mg per day. The treatment duration will range from 6 to 12 months. A control group will be used to correlate the outcome-parameters for a descriptive comparison. The control group includes patients with IPF on the waiting list who were on another IPF specific (or no) treatment for IPF The Study Population are Patients aged between 40-70 years who are admitted to the lung transplantation department and fulfill the international criteria for idiopathic pulmonary fibrosis ( existence of a usual interstitial pneumonia (UIP) pattern in the high-resolution computed tomography (HRCT) is necessary).

Read more

Variables: Duration of mechanical ventilation after LUTX (hours), Forced Vital capacity relative to reference value at baseline (FVC0%), Forced Vital capacity relative to reference value after 6 months (FVC6%),Forced Vital capacity relative to reference value after 12 months (FVC12%) Study Size: 30 patients in the Pirfenidone group, 20 patients in the control group.

For the primary Endpoint, the mean, standard deviation, median, minimum and maximum of the weaning time of patients who received a pirfenidone treatment, as well as of patients from the control group will be computed and presented in a table. Additionally, a Kaplan-Meier curve will be estimated and plotted alongside the respective 95% CI calculated using the method of Brookmeyer and Crowley. Furthermore, a stepwise linear regression using forward selection and Age, RBMI, FVC0%, (FVC6%-FVC0%), TLC, FEV1% and ECMO, as well as the pirfenidone treatment as predictors will be computed. The null hypothesis is that the pirfenidone treatment has no influence on the weaning time. The according model coefficient estimate and standard error will be used to test the null hypothesis using a t-test at significance level α=0.05.

For the secondary endpoints, the mean, standard deviation, median, minimum and maximum of patients who received a pirfenidone treatment, as well as of patients from the control group will be computed and presented in a tableStepwise Cox Regression using forward selection and Age, RBMI, FVC0%, (FVC6%-FVC0%) and ECMO, as well as the pirfenidone treatment as predictors will be computed in order to compare the treatment and the control group a . If p-values are calculated for the secondary endpoint analysis, they serve only descriptive purposes. Therefore no multiple testing corrections are applied.

Medical subject headings
Idiopathic Pulmonary Fibrosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03258801
Study groupRoleWhat they receive
PirfenidonePatients who are admitted to the lung transplantation department and fulfill the international criteria for idiopathic pulmonary fibrosis and are treated with Pirfenidone as bridging therapy.
ControlPatients who are admitted to the lung transplantation department and fulfill the international criteria for idiopathic pulmonary fibrosis and are not treated with Pirfenidone.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Duration time of mechanical ventilation (weaning) directly after lung transplantation

    Duration of mechanical ventilation after LUTX measured in days

    Measured: First two weeks after lung transplantation

Secondary outcomes (4)
  1. Days of survival after LUTX

    Days of survival after LUTX measured in days

    Measured: First 90 days after LUTX

  2. decline in forced vital capacity (FVC%) from baseline to 6 months

    decline in forced vital capacity (FVC%) from baseline to 6 months

    Measured: from baseline to 6 months

  3. decline in forced vital capacity (FVC%) from baseline to 12 months

    decline in forced vital capacity (FVC%) from baseline to 12 months

    Measured: from baseline to 12 months

  4. decline in forced vital capacity (FVC%) from 6 months to 12 months

    decline in forced vital capacity (FVC%) from 6 months to 12 months

    Measured: from 6 months to 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Aug 2017
  2. Study start29 Oct 2018
  3. Primary completion2 Dec 2019
  4. Study completion2 Dec 2019

Why it stopped: Clinical evaluation plan outdated and obsolete due to altered clinical routine

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03258801
Sponsor's protocol ID
NIS-ML-29952
Status last verified
Jan 2020
First submitted
18 Aug 2017
Last updated
27 Jan 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Idiopathic Pulmonary Fibrosis and Lung Transplant; Complications, run by Dr. Christopher Lambers at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 27 Jan 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Duration time of mechanical ventilation (weaning) directly after lung transplantation (time frame: First two weeks after lung transplantation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jan 2020.

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