The PALP™-COPD Trial (Low-Flow CO2-Removal (ECCO2-R) in Exacerbated COPD)

Not Applicable

Withdrawn

• Conditions: COPD; Chronic Obstructive Pulmonary Disease
• Interventions: Device: CO2-Removal (PALP-Device/MaquetCP)

• Registration Number: NCT02107222
• Lead Sponsor: Maquet Cardiopulmonary GmbH

Brief Summary

A Multicenter, Randomized, Controlled Trial to Determine Safety and Efficacy of Pump Assisted Lung Protection (PALP™) for Low Flow Carbon Dioxide (CO2) Removal in Conjunction with Liberation from Mechanical Ventilation Compared to Mechanical Ventilation Alone in Patients with COPD Exacerbation and Respiratory Failure

Detailed Description

Primary Study Objectives

• To evaluate the clinical effect of PALP™ in reducing the time on invasive ventilation in patients with an exacerbation of COPD requiring invasive mechanical ventilation.

Secondary Study Objectives

* To evaluate the safety and tolerability of PALP™ in patients with an exacerbation of COPD requiring invasive mechanical ventilation.

* To determine if rates of adverse events (AEs) are reduced in patients who receive PALP™ and invasive mechanical ventilation vs invasive mechanical ventilation alone.

* To determine mortality rates in patients who receive PALP™ and invasive mechanical ventilation vs invasive mechanical ventilation alone.

* To determine if PALP™ will effectively reduce the number of subsequent acute decompensations requiring hospital admission for ventilatory support (invasive or noninvasive).

Study Timeline

• Study First Submitted: 2014-03-28
• Study First Submitted QC: 2014-04-04
• Study First Posted: 2014-04-08
• Status Verified: 2016-03
• Last Update Submitted: 2016-03-31
• Last Update Posted: 2016-04-01
• Primary Completion: 2016-12

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1. Male or female, and ≥40 years of age
2. Known history of COPD
3. Currently experiencing an exacerbation of COPD
4. P/F ratio >150 mmHg
5. Currently endotracheally intubated and requiring invasive mechanical ventilation (must have been on invasive mechanical ventilation for 24-48 hours)
6. Able to tolerate large bore intravenous (IV) cannulation required for proper operation of study device
7. For female patients of child-bearing potential, a negative urine or serum pregnancy test at screening; all female patients will be considered of child-bearing potential unless they are post menopausal for at least 1 year or have been surgically sterilized (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy)
8. Written informed consent obtained according to local regulations; or, if unable to provide written informed consent due to incapacitation, a legally authorized representative is able to provide written informed consent on behalf of the patient

Exclusion Criteria

1. Any end-stage medical conditions with expected survival <6 months

2. Tracheostomy

3. Unable to provide central venous access

4. Acute brain injury

5. Any legally authorized document(s) that may restrict aggressive medical management such as "Do Not Resuscitate," "Do Not Intubate," etc.

6. Risk of bleeding or clotting such as:

   • Known bleeding diathesis or abnormal clotting
   • Recent or current use of medications known to increase risk of bleeding

7. Screening platelet count of <75,000/mm3 or international normalized ratio (INR) >1.5 or activated partial thromboplastin time (aPTT) >1.5 times the upper limit of normal (ULN) range for their respective laboratory values

8. Any recognized contra indications to systemic anticoagulation therapy or use of heparin

9. Body mass index (BMI) >35

10. Any form of chronic hyperventilation not related to COPD

11. Hemodynamic instability or requiring significant vasopressor support

12. Cardiogenic or noncardiogenic pulmonary edema as the primary reason for respiratory failure

13. High risk cardiac conditions

14. Oxygen tension in arterial blood (PaO2) <50 mmHg via arterial blood gas (ABG) or any condition in which hypoxemia is a significant component of the respiratory failure

15. Any other medical cause for acute respiratory failure not directly related to a COPD exacerbation

16. Use of or treatment with an investigational drug, therapy, or device within 1 month (30 days) of baseline

17. Female patients who are pregnant or breastfeeding

18. Patients who are immuno-compromised

19. Current active malignancy or history of malignancy within the past 5 years

20. Patients in chronic dialysis

21. Patients requiring extra-corporeal life support (ECLS) as a bridge to transplant

22. Patients who, in the opinion of the investigator, would not be able to comply with the requirements of the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
MV + ECCO2-R(PALP-Device/MaquetCP)	CO2-Removal (PALP-Device/MaquetCP)	MV according to the guidelines plus CO2-Removal with PALP

Primary Outcome Measures

Name	Time	Method
Difference in time of mechanical ventilation	720 hours	• To evaluate the clinical effect of PALP™ in reducing the time on invasive ventilation in patients with an exacerbation of COPD requiring invasive mechanical ventilation.

Trial Locations

Locations (1)

MAQUET Cardiopulmonary AG; 🇩🇪 Rastatt, Germany