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Giessen Pulmonary Hypertension in Lung Cancer Registry

Giessen Pulmonary Hypertension in Lung Cancer Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04467333
Acronym
PHLHR
Enrollment
500
Registered
2020-07-13
Start date
2020-06-29
Completion date
2040-01-29
Last updated
2025-04-01

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

Conditions

Pulmonary Hypertension Due to Lung Diseases and Hypoxia

Brief summary

The aim of this study is to investigate the frequency and implications of pulmonary hypertension in lung cancer patients. To do so, data will be collected from all lung cancer patients at the university hospital Giessen. All data will be analyzed for possible hints of pulmonary hypertension as a comorbidity in lung cancer patients. All information will be generated from the regular guidelines based course of treatment and there will be no interventions. This study will serve as a prospective register for all lung cancer patients treated at the university hospital Giessen.

Interventions

OTHERAll lung cancer patients.

There will be no specific interventions. All patients will receive guidelines based therapy of lung cancer and their comorbidities.

Sponsors

University of Giessen
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

* Patient with lung cancer at the University of Giessen lung Cancer Center.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Pulmonary function test measured via Spirometry.2 yearsvital capacity, total lung capacity, forced expiratory volume in one second, functional vital capacity, diffusing capacity for carbon monoxide, arterial partial pressure of oxygen; all measured as % of predicted normal values.
sPAP values measured via Echocardiography.2 yearssystolic pulmonary artery pressure (sPAP) measured in millimetre of mercury (mmHg).
Body mass index.2 yearsweight and height will be combined to report BMI in kg/m\^2.
Overall Survival and Progression Free Survival measured in days.2 yearsOverall Survival and Progression free survival in days will be determined by Kaplan-Meier Analysis .Measuared in (st) (time from diagnosis to death)
Measurements of the pulmonary artery diameter (PA) and ascending aorta (AA) diameter measured via computed tomography scan. PA and AA will be measured in millimeters.2 yearsPA and AA will be combined to report the PA/AA quotient as indicator for pulmonary hypertension in all lung cancer patients. With a cut off value of ≥ 1 defining pulmonary hypertension.
6 Minute Walk Test in meters.2 yearsThe 6 minute walk test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance in meters covered over a time of 6 minutes is used as the outcome.
Modified Medical Research Council Scale (mMRC).2 yearsScores on the mMRC reach from 0-4, with higher scores indicating greater dyspnea.
chronic obstructive pulmonary disease assessment test (CAT).2 yearsScores on the CAT reach from 0-40, with higher scores indicating greater dyspnea.

Countries

Germany

Contacts

Primary ContactBastian Eul, MD
bastian.eul@innere.med.uni-giessen.de(+49) 0641/985-42371
Backup ContactMichael John Cekay, MD
michael.cekay@innere.med.uni-giessen.de

Outcome results

None listed

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