search
Back to results

Protocol for the Infusion of Buffy Coat-derived Cryopreserved Platelets in Patients With Severe Thrombocytopenia (MICE)

Primary Purpose

Thrombocytopenia, Primary Thrombocytopenia,Unspecified, Thrombocytopenia Chemotherapy Induced

Status
Terminated
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Transfusion of Pooled Platelets Cryopreserved In DMSO
Sponsored by
Napolitano Mariasanta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Thrombocytopenia focused on measuring Cryopreserved platelets, thrombocytopenia, DMSO

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Cryopreserved buffy coat pooled platelets will be infused, after being thawed, in inpatients at U.O. of Hematology -Policlinic "P. Giaccone"-Palermo, falling into one of the following categories:

  • Stable clinical conditions and no complications with platelets ≤ 10,000/microliter;
  • With active bleeding and ≤ 20,000 platelets/microliter;
  • In the presence of: high blood pressure, high fever, rapid drop in platelets, infection, chemotherapy, coagulation abnormalities with ≤ 20,000 platelets/microliter.

Exclusion Criteria:

Patients

  • Suffering from congenital immunodeficiency
  • Allogeneic bone marrow transplant candidates
  • Bone Marrow Donors for transplantation
  • Undergoing bone marrow transplant or
  • Suffering from Hodgkin's disease and treated with purine analogues (Fludarabine, cladribine)

Sites / Locations

  • AOUP "P.Giaccone"-Hematology Unit

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patients with severe thrombocytopenia

Arm Description

Intervention Patients with severe thrombocytopenia with an active bleeding, in preparation for surgery, or after chemotherapy (prophylaxis of bleeding),will receive transfusion of Pooled Platelets Cryopreserved In DMSO With a New System

Outcomes

Primary Outcome Measures

Efficacy of infused cryopreserved platelets (changes in platelets count will be determined at 1 hour and 24 hours post-transfusion)
To evaluate the availability of cryopreserved platelets after transfusion, the correct count (the number of platelets poured and the body surface, BMI, recipient) of platelets will be determined at 1 hour and 24 hours post transfusion, respectively

Secondary Outcome Measures

Safety of cryopreserved platelets
Any transfusion-related side effect (i.e. idiosyncrasy, allergy, toxicity) will be monitored

Full Information

First Posted
January 7, 2014
Last Updated
October 17, 2017
Sponsor
Napolitano Mariasanta
Collaborators
Regione Sicilia
search

1. Study Identification

Unique Protocol Identification Number
NCT02032134
Brief Title
Protocol for the Infusion of Buffy Coat-derived Cryopreserved Platelets in Patients With Severe Thrombocytopenia
Acronym
MICE
Official Title
Experimental Protocol for the Infusion of Platelets,Cryopreserved With Dimethyl Sulphoxide (DMSO) and Obtained From Multiple Donors Buffy Coats, in Patients With Severe Thrombocytopenia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
recruitment failure within the interval of available CRY BC-PLTs for the study
Study Start Date
July 2015 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Napolitano Mariasanta
Collaborators
Regione Sicilia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The increasing need for blood components and the increasingly careful donor selection procedures, make the availability of blood components very reduced, in particular for platelets that are currently administered preferably "fresh" or cryopreserved, only in emergency conditions. Exceeding this limit through the spread of use of cryopreserved platelets in the common clinical practice, might help clinicians to avoid wasting valuable products and face periods of particular shortage of donors Some studies already published in the literature over the last decade (1,2) have demonstrated the safety and efficacy of autologous cryopreserved platelets . The main objective of the proposed study is to evaluate the efficacy and safety of platelets, cryopreserved with DMSO using a a new method, in patients with severe thrombocytopenia. This is the in vivo phase of a study where availability and efficacy of cryopreserved platelets has been assessed in vitro.
Detailed Description
The primary objective of the study is to evaluate the hemostatic efficacy and safety in the recipients of platelets obtained from buffy coat of multiple donors (five), cryopreserved with DMSO using a new patented method, up to 9 months from the collection. Further goals are the registration of any related- adverse event (idiosyncrasy, allergy, toxicity)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thrombocytopenia, Primary Thrombocytopenia,Unspecified, Thrombocytopenia Chemotherapy Induced
Keywords
Cryopreserved platelets, thrombocytopenia, DMSO

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients with severe thrombocytopenia
Arm Type
Other
Arm Description
Intervention Patients with severe thrombocytopenia with an active bleeding, in preparation for surgery, or after chemotherapy (prophylaxis of bleeding),will receive transfusion of Pooled Platelets Cryopreserved In DMSO With a New System
Intervention Type
Biological
Intervention Name(s)
Transfusion of Pooled Platelets Cryopreserved In DMSO
Other Intervention Name(s)
New Cryopreservation kit (Promedical ®), Buffy Coat Pooled Platelets Cryopreserved In DMSO
Intervention Description
Patients with severe thrombocytopenia will be admitted as in patients at the Hematology Unit of the Policlinic "P. Giaccone"- Palermo, if they require platelet transfusion (for bleeding, in preparation for surgery, after chemotherapy); they will receive buffy coat derived cryopreserved platelets,after thawing
Primary Outcome Measure Information:
Title
Efficacy of infused cryopreserved platelets (changes in platelets count will be determined at 1 hour and 24 hours post-transfusion)
Description
To evaluate the availability of cryopreserved platelets after transfusion, the correct count (the number of platelets poured and the body surface, BMI, recipient) of platelets will be determined at 1 hour and 24 hours post transfusion, respectively
Time Frame
1 Hour and 24 hours post-transfusion
Secondary Outcome Measure Information:
Title
Safety of cryopreserved platelets
Description
Any transfusion-related side effect (i.e. idiosyncrasy, allergy, toxicity) will be monitored
Time Frame
During transfusion and within 48 hours after transfusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cryopreserved buffy coat pooled platelets will be infused, after being thawed, in inpatients at U.O. of Hematology -Policlinic "P. Giaccone"-Palermo, falling into one of the following categories: Stable clinical conditions and no complications with platelets ≤ 10,000/microliter; With active bleeding and ≤ 20,000 platelets/microliter; In the presence of: high blood pressure, high fever, rapid drop in platelets, infection, chemotherapy, coagulation abnormalities with ≤ 20,000 platelets/microliter. Exclusion Criteria: Patients Suffering from congenital immunodeficiency Allogeneic bone marrow transplant candidates Bone Marrow Donors for transplantation Undergoing bone marrow transplant or Suffering from Hodgkin's disease and treated with purine analogues (Fludarabine, cladribine)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sergio Siragusa, MD
Organizational Affiliation
Hematology Unit- University of Palermo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mariasanta Napolitano, MD
Organizational Affiliation
Hematology Unit- University of Palermo
Official's Role
Principal Investigator
Facility Information:
Facility Name
AOUP "P.Giaccone"-Hematology Unit
City
Palermo
State/Province
Regione Sicilia
ZIP/Postal Code
90127
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
12493312
Citation
Wautier JL. Safety and usefulness of autologous cryopreserved platelets. Lancet. 2002 Dec 14;360(9349):1985. doi: 10.1016/S0140-6736(02)11893-9. No abstract available.
Results Reference
background
PubMed Identifier
22781890
Citation
Liu GQ, Ding HF, Lu XJ, Xu M, Xing J, Zhao X, Han F, Shang YH. [The efficacy and safety of autologous cryopreserved platelet transfusion in management of thrombocytopenia after chemotherapy in hematological malignancy]. Zhonghua Nei Ke Za Zhi. 2012 Mar;51(3):188-91. Chinese.
Results Reference
background
PubMed Identifier
15183900
Citation
Heal JM, Blumberg N. Optimizing platelet transfusion therapy. Blood Rev. 2004 Sep;18(3):149-65. doi: 10.1016/S0268-960X(03)00057-2.
Results Reference
background
PubMed Identifier
1339584
Citation
Murphy MF, Brozovic B, Murphy W, Ouwehand W, Waters AH. Guidelines for platelet transfusions. British Committee for Standards in Haematology, Working Party of the Blood Transfusion Task Force. Transfus Med. 1992 Dec;2(4):311-8. doi: 10.1111/j.1365-3148.1992.tb00175.x.
Results Reference
background
PubMed Identifier
22671278
Citation
Dumont LJ, Cancelas JA, Dumont DF, Siegel AH, Szczepiorkowski ZM, Rugg N, Pratt PG, Worsham DN, Hartman EL, Dunn SK, O'Leary M, Ransom JH, Michael RA, Macdonald VW. A randomized controlled trial evaluating recovery and survival of 6% dimethyl sulfoxide-frozen autologous platelets in healthy volunteers. Transfusion. 2013 Jan;53(1):128-37. doi: 10.1111/j.1537-2995.2012.03735.x. Epub 2012 Jun 7.
Results Reference
background
PubMed Identifier
23003345
Citation
Meyer E, Delaney M, Lin Y, Morris A, Pavenski K, Tinmouth A, Murphy M, Slichter SJ, Heddle N, Dumont LJ. A reporting guideline for clinical platelet transfusion studies from the BEST Collaborative. Transfusion. 2013 Jun;53(6):1328-34. doi: 10.1111/j.1537-2995.2012.03906.x. Epub 2012 Sep 25.
Results Reference
background
PubMed Identifier
21214584
Citation
Dumont LJ, Dumont DF, Unger ZM, Siegel A, Szczepiorkowski ZM, Corson JS, Jones MK, Christoffel T, Pellham E, Bailey SL, Slichter SJ; BEST Collaborative. A randomized controlled trial comparing autologous radiolabeled in vivo platelet (PLT) recoveries and survivals of 7-day-stored PLT-rich plasma and buffy coat PLTs from the same subjects. Transfusion. 2011 Jun;51(6):1241-8. doi: 10.1111/j.1537-2995.2010.03007.x. Epub 2011 Jan 7.
Results Reference
background
PubMed Identifier
31753773
Citation
Napolitano M, Mancuso S, Raso S, LoCoco L, Arfo PS, De Francisci G, Dieli F, Caccamo N, Reina A, Dolce A, Agliastro R, Siragusa S. Buffy coat-derived platelets cryopreserved using a new method: Results from a pivotal clinical trial on thrombocytopenic patients with acute leukaemia. Transfus Apher Sci. 2019 Dec;58(6):102666. doi: 10.1016/j.transci.2019.10.008. Epub 2019 Nov 5.
Results Reference
derived

Learn more about this trial

Protocol for the Infusion of Buffy Coat-derived Cryopreserved Platelets in Patients With Severe Thrombocytopenia

We'll reach out to this number within 24 hrs