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Immunoadsorption in Patients With Pulmonary Hypertension

Randomized, Prospective Investigation on the Effects of Immunoadsorption on Pulmonary Vascular Resistance in Patients With Pulmonary Hypertension

Status
Withdrawn
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01126411
Enrollment
0
Registered
2010-05-19
Start date
2009-10-31
Completion date
2013-12-31
Last updated
2016-11-16

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

Conditions

Pulmonary Hypertension, Pulmonary Resistance

Keywords

pulmonary hypertension, autoantibodies, immunoadsorption, immunoglobulin substitution, right ventricular function

Brief summary

The purpose of this study is to investigate, if Immunoadsorption of autoantibodies with subsequent substitution of immunoglobulins is able to improve haemodynamics in patients with pulmonary hypertension.

Detailed description

Increased pulmonary precapillary vascular resistance due to vasoconstriction and vasoproliferative processes is the basic pathophysiological mechanism in the development of pulmonary hypertension (PH). In patients with pulmonary arterial hypertension (PH) production of endothelin-1 (ET-1) is increased and elevated ET-1 plasma levels correlate with PH severity As recently shown Autoantibodies against the Endothelin-1 Typ A and Angiotensin II Typ-1 Receptor, which have a high Incidence in PH-Patients, may also play an important role in the pathophysiology of PH (Dandel et al.). The concept of this study is that the elimination of these autoantibodies by Immunoadsorption with protein A may improve haemodynamics and patient wellbeing. Immunoglobulins are substituted after Immunoadsorption to minimize infection risk.

Interventions

PROCEDUREimmunoadsorption / immunglobulin substitution

Immunoadsorption with protein-A columns on five consecutive days with subsequent human polyclonal immunoglobulin G substitution after day 5 (0,5g /kg bodyweight)

Sponsors

University Medicine Greifswald
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* pulmonary hypertension (PH) * NYHA II-IV * medical treatment of PH respective to current guidelines * 18 years or older * written informed consent of the patient

Exclusion criteria

* pulmonary hypertension due to left ventricular dysfunction * decompensated heart failure * need for Catecholamines * active infection * pregnancy * malign tumor disease * other secondary disease with life expectancy \< 1 year * refusal by the patient

Design outcomes

Primary

MeasureTime frameDescription
pulmonary vascular Resistance3 monthThe extend of change of pulmonary vascular resistance over the observation period will be compared between the 2 groups (treatment versus control group).

Secondary

MeasureTime frameDescription
NYHA3 monthNYHA = functional capacity. The extent of change of NYHA-class over the observation period will be compared between the 2 groups (treatment versus control group).
nt pro BNP3 monthnt pro BNP = B-type natriuretic peptide. The extent of change of nt-pro BNP over the observation period will be compared between the 2 groups (treatment versus control group).
peak oxygen uptake (spiroergometry)3 monthThe extent of change of peak oxygen uptake over the observation period will be compared between the 2 groups (treatment versus control group).
6 min walktest3 monthThe extent of change of 6-min walktest over the observation period will be compared between the 2 groups (treatment versus control group).
echocardiographic parameters: TAPSE3 monthTAPSE=excursion of the lateral tricuspid annulus (measured in m-mode). the extend of cange of TAPSE over the observationperiod will be compared between the 2 groups (treatment vs. controlgroup)
echocardiographic parameters: PAPs3 monthPAPs = systolic pulmonalarterial pressure estimated by maximal flow velocity of tricuspid regurgitant jet (continues doppler). The extent of change of PAPs over the observation period will be compared between the 2 groups (treatment versus control group).
electrocardiographic parameters: S´lat. TR Annulus3 monthS´lat. TR Annulus = systolic velocity of the lateral tricuspid annulus measured by tissue doppler. The extent of change of S´ lat. TR Annulus over the observation period will be compared between the 2 groups (treatment versus control group).
echocardiographic parameters: AT right ventricular outflow3 monthAT right ventricular outflow = acceleration time of right ventricular outflow, measured by pulsed wave doppler echocardiography. The extent of change of AT over the observation period will be compared between the 2 groups (treatment versus control group).
ET-1 TYP A Receptor Autoantibody level3 monthThe extent of change of ET-1 TYP A Receptor Autoantibody level over the observation period will be compared between the 2 groups (treatment versus control group).

Countries

Germany

Outcome results

None listed

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