Pocket Haematoma Prevention in Patients Who Required Implantation/Replacement of a Pacemaker or Implantable Cardiac Defibrillator. The PHP Study. (PHP)
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|ClinicalTrials.gov Identifier: NCT01127984|
Recruitment Status : Completed
First Posted : May 21, 2010
Last Update Posted : February 11, 2011
The aim of this study is to demonstrate the efficacy of fibrin sealant (Tissucol-Baxter) in preventing pocket haematoma and subsequent complications in patients undergoing pacemaker or ICD implantation/replacement which cannot discontinue dual antiplatelet therapy (i.e. ASA and clopidogrel, ASA and prasugrel) or anticoagulant therapy (i.e. warfarin, heparin, low molecular weight heparin).
Fibrin-based sealant is available for local haemostasis. A recent study (Milic DJ et al, 2005 Europace, 7: 374-379) has shown the efficacy of the fibrin sealant in prevention of pacemaker pocket haematoma in 40 patients undergoing pacemaker implantation who are receiving anticoagulant treatment.
Patients with dual antiplatelet therapy (DAT) are prone to a high risk of bleeding during surgical procedures. Thus, the routine use is the discontinuation of DAT al least 4-7 days before the intervention. This practice may result in a high risk of thrombotic events in patients with coronary stenting.
Recently, in our Center we started the use of a fibrin sealant for local haemostasis (Tissucol Baxter), and the investigators observed a reduction in the incidence of pocket haematoma complication, the need of vacuum drainage system, and the reduction of hospital stay.
|Condition or disease||Intervention/treatment||Phase|
|Pacemaker Implantation Pocket Hematoma and Bleeding Antiplatelet Therapy or Oral Anticoagulants||Drug: tissucol Procedure: drainage system||Phase 4|
Purpose of the study. The purpose of this study is to demonstrate the efficacy of a fibrin sealant (Tissucol-Baxter) in prevention pocket haematoma and subsequent complications in patients who required implantation/replacement of a pacemaker or ICD wich cannot discontinue dual antiplatelet or anticoagulant therapy.
Target. The primary endpoint is to test the impact of pocket haematoma in patients treated with tissucol compared to a conventional treatment with vacuum drainage system without dual antiplatelet or anticoagulant therapy discontinuation.
The secondary endpoint is to compare the length of hospitalization between the two groups.
Type of study. Prospective, randomized, single center, open label.
Materials and methods. Will be consecutively enrolled approximately 100 patients.
Inclusion criteria: patients over the age of eighteen who require an initial implantation or replacement of a device (pacemaker, biventricular pacemaker, ICD) treated with:
- dual antiplatelet therapy (clopidogrel or prasugrel or ticlopidine, and acetylsalicylic acid) or
- anticoagulants (warfarin or heparin or low molecular weight heparin). Patients Do not discontinue the antiplatelet or anticoagulant therapy.
According to a randomization list, patients will be assigned to tissucol treatment or vacuum drainage system:
- 50 patients: treated with local application of tissucol in the pocket of pacemaker/ICD;
- 50 patients: treated with vacuum drainage system.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||100 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Pocket Haematoma Prevention in Patients Who Required Implantation/Replacement of a Pacemaker or Implantable Cardiac Defibrillator (ICD) During Dual Antiplatelet or Anticoagulant Therapy. A Prospective Randomized Trial. The PHP Study.|
|Study Start Date :||December 2009|
|Actual Primary Completion Date :||January 2011|
|Actual Study Completion Date :||January 2011|
Experimental: treatment with tissucol
patients treated with tissucol, local application in the pocket of PM / ICD
dosage: 2 or 5 ml Frequency: 1 application Duration: 5 minutes
Other Name: local tissucol application
Active Comparator: vacuum drainage system
patients treated with application of vacuum drainage system.
Procedure: drainage system
application of vacuum drainage system
Other Name: vacuum drainage system
- Complications of pocket device: haematoma and bleeding.Pocket haematoma is defined as palpable swelling of the device pocket exceeding the size of the generator.Bleeding is defined as > 100 ml amount of fluid collected in the drainage system. [ Time Frame: 45 days after intervention ]
- The duration of the hospital stay [ Time Frame: 45 days after intervention ]
- The number of outpatient visits following the hospitalization [ Time Frame: 45 days after intervention ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01127984
|Division of Invasive Cardiology 1, Careggi Hospital|
|Florence, Italy, 50134|
|Principal Investigator:||Emilio V Dovellini, MD||Division of Invasive Cardiology, Careggi Hospital|