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Prospective, Multicenter, Multidisciplinary, Controlled Clinical Investigation Evaluating the Safety and Efficacy of PerClot® Polysaccharide Hemostatic System (CLOT)

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ClinicalTrials.gov Identifier: NCT02359994
Recruitment Status : Active, not recruiting
First Posted : February 10, 2015
Last Update Posted : January 17, 2019
Sponsor:
Information provided by (Responsible Party):
CryoLife, Inc.

February 3, 2015
February 10, 2015
January 17, 2019
April 2015
January 2019   (Final data collection date for primary outcome measure)
Achievement of hemostasis [ Time Frame: 7 minutes following application ]
The primary objective of this clinical investigation is to demonstrate non-inferiority in the achievement of hemostasis of the treated bleeding site at 7 minutes in subjects receiving PerClot compared to those receiving a control hemostatic device. The primary endpoint is the proportion of subjects achieving hemostasis of the treated lesion at 7 minutes in each treatment group.
Achievement of hemostasis [ Time Frame: 7 minutes following application ]
Hemostasis is defined as complete cessation of bleeding. If the surgeon visually observes complete cessation of bleeding, this will be considered successful hemostasis; If the surgeon visually observes bleeding egressing from the randomized study device, this will be considered a failure of hemostasis.
Complete list of historical versions of study NCT02359994 on ClinicalTrials.gov Archive Site
Achievement of hemostasis [ Time Frame: 5 minutes following application ]
The secondary objective of this investigation is to compare the achievement of hemostasis of the treated bleeding site at 5 minutes for subjects receiving PerClot compared to those receiving a control hemostatic device. The secondary endpoint is the proportion of subjects achieving hemostasis of the treated bleeding site at 5 minutes in each treatment group.
Not Provided
Not Provided
Not Provided
 
Prospective, Multicenter, Multidisciplinary, Controlled Clinical Investigation Evaluating the Safety and Efficacy of PerClot® Polysaccharide Hemostatic System
Prospective, Multicenter, Multidisciplinary, Controlled Clinical Investigation Evaluating the Safety and Efficacy of PerClot® Polysaccharide Hemostatic System

This is a prospective, multicenter, multidisciplinary, controlled clinical investigation evaluating the safety and efficacy of PerClot in achieving intraoperative hemostasis compared to a similar marketed hemostatic device.

Three hundred and twenty four subjects across a maximum of 25 investigational sites undergoing open elective cardiac, general, or urological surgical procedures who meet the eligibility criteria will be intraoperatively randomized to receive no more than the entire contents of up to two 5 gram bellows of either the investigational device or a control hemostatic agent on a bleeding site, whose anatomic site is smaller than or equal to 25cm² and whose anatomic application site is smaller than or equal to 47cm², when bleeding is within the pre-defined bleeding severity range after any applicable conventional means for hemostasis are attempted as specified in the intraoperative procedures.

Each investigational site is expected to enroll approximately 13-40 subjects. All investigational sites will be located in the U.S. Follow-up will occur at hospital discharge and 6 weeks post-device application. For oncologic subjects, an additional follow up will occur at 24 months post device application.

Not Provided
Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Blood Loss, Surgical
  • Device: PerClot Polysaccharide Hemostatic System
    During the intraoperative period, the subject will be evaluated for bleeding; only those who meet the intraoperative inclusion criterion will be enrolled into the study. After confirmation of the intraoperative eligibility criteria, the subject will be randomized to receive an adjunct application of PerClot or the control device. The prescribed hemostatic agent will be applied according to its Instructions for Use.
  • Device: Arista AH
    During the intraoperative period, the subject will be evaluated for bleeding; only those who meet the intraoperative inclusion criterion will be enrolled into the study. After confirmation of the intraoperative eligibility criteria, the subject will be randomized to receive an adjunct application of PerClot or the control device. The prescribed hemostatic agent will be applied according to its Instructions for Use.
  • Experimental: Cardiac Surgery
    For cardiac procedures, the site of evaluation for satisfaction of intraoperative eligibility criteria will be any bleeding sites on the epicardium, along an aortic anastomotic suture line, or an aortotomy suture line. For example, the surgeon will perform dissection of adhesions per his or her conventional methods and bleeding will be controlled using means continually employed by the surgeon prior to surgical closure. Prior to application along an aortic anastomotic suture line or an aortotomy suture line, suture line gaps > 2mm and large needle holes > 2mm will be ligated prior to assessment of intraoperative eligibility criteria. Any bleeding site on the epicardium, or along an aortic anastomotic suture line, or an aortotomy suture line meeting the eligibility criteria will be evaluated for satisfaction. PerClot should be applied after drug reversal and the patient is taken off by-pass.
    Interventions:
    • Device: PerClot Polysaccharide Hemostatic System
    • Device: Arista AH
  • Experimental: General Surgery

    For liver resection procedures, the resected liver surface will be the site of evaluation. The surgeon will perform resection of the diseased portion of the liver per his/her conventional methods. Bleeding from discrete vessels will be controlled using means conventionally employed by the surgeon. Vessels > 2mm in diameter will be ligated and any observed bile leaks controlled prior to assessment of intraoperative eligibility criteria.

    For total splenectomy procedures, the site of evaluation for satisfaction of the intraoperative eligibility criteria will be the retroperitoneal surface. The surgeon will perform the splenectomy per his/her conventional methods. Vessels > 2mm in diameter will be ligated prior to assessment of intraoperative eligibility criteria.

    Any bleeding site on the retroperitoneal surface/cavity or exposed parenchymal surface will be evaluated for satisfaction of the eligibility criteria.

    Interventions:
    • Device: PerClot Polysaccharide Hemostatic System
    • Device: Arista AH
  • Experimental: Urologic Surgery

    For on-clamp partial nephrectomies, the site of evaluation will be the kidney bed surface. The surgeon will perform resection of the kidney per his or her conventional methods. Vessels > 2mm in diameter will be ligated and entries into the collecting system controlled prior to assessment of intraoperative eligibility criteria. Any bleeding site on the kidney bed will be evaluated for satisfaction of the eligibility criteria after clamp release.

    For radical nephrectomies, the site of evaluation will be the retroperitoneal surface/cavity. The surgeon will perform the procedure per his or her conventional methods. Vessels > 2mm in diameter will be ligated prior to assessment of intraoperative eligibility criteria. Any bleeding site on the retroperitoneal surface/cavity will be evaluated for satisfaction of the eligibility criteria.

    Interventions:
    • Device: PerClot Polysaccharide Hemostatic System
    • Device: Arista AH
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
324
Same as current
March 2019
January 2019   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Preoperative inclusion:

    • Subject is undergoing one of the following open elective cardiac, general, or urological surgical procedures: Cardiac procedure (Epicardium); Cardiac procedure (aortic anastomosis or aortotomy suture line); Liver resection; Total splenectomy; On-clamp partial nephrectomy; or Radical nephrectomy.
    • Subject is willing and able to give prior written informed consent for investigation participation; and
    • Subject is > 22 years of age.
  • Intraoperative inclusion:

    • Subject is undergoing one of the following elective procedures: Cardiac procedure (Epicardium); Cardiac procedure (Aortic Anastomosis or Aortotomy suture line); Liver resection; Total splenectomy; On-clamp partial nephrectomy; or Radical nephrectomy.
    • Subject in whom all visible vessels or suture holes greater than or equal to 2mm in diameter have been ligated;
    • Subject in whom there is bleeding at the specified area for each surgical procedure after any applicable conventional means for hemostasis are attempted as specified by the intraoperative protocol;
    • Subject in whom the anatomic site is equal to or less than 25cm²;
    • Subject in whom the anatomic application site is equal to or less than 47cm²; and
    • Subject in whom the bleeding flux from the identified lesion is > 0.000040[g/(cm²•s)] and ≤0.013[g/(cm²•s)].

Exclusion Criteria:

  • Preoperative Exclusion Criteria

    • Subject with known sensitivity to starch or starch-derived materials;
    • Subject who has a clinically significant coagulation disorder or disease, defined as a platelet count <100,000 per microliter, International Normalized Ratio >1.5, or a PTT more than 1.5 times outside the laboratory's normal reference range;
    • Subject who used corticosteroids (excluding inhalers, eye-drops, and dermatologic corticosteroids) within 6 weeks prior to surgery;
    • Subject who has been treated with an investigational product and has not completed the entire follow-up period for that investigational product;
    • Subject who is pregnant (as confirmed by pregnancy test), planning on becoming pregnant during the follow-up period, or actively breast-feeding; and
    • Subject with poor blood glucose control as per glycosylated hemoglobin > 9%.
  • Intraoperative Exclusion Criteria

    • Subject undergoing a cardiac procedure in which there is no aortic anastomosis or aortotomy suture line to evaluate using the bleeding severity scale (i.e., not for treatment at the distal coronary artery bypass graft anastomosis);
    • Subject in whom any major intraoperative bleeding incidences during the surgical procedure occurred (i.e., subject with assignment of an American College of Surgeons Advanced Trauma Life Support Hemorrhage Class of II, III, or IV Hemorrhage);
    • Subject who has an active or potential infection at the surgical site, or whose surgical wound is defined as a wound classification of CO (Contaminated) or D (Dirty or Infected) based upon the Center for Disease Control and Prevention's wound classification system; and
    • Subject who has undergone platelet receptor GP IIb/IIIa antagonist therapy less than 48 hours prior to surgery.
Sexes Eligible for Study: All
22 Years and older   (Adult, Older Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT02359994
PCT1101.011-C(02/15)
Yes
Not Provided
Not Provided
CryoLife, Inc.
CryoLife, Inc.
Not Provided
Principal Investigator: Michael House, MD Indiana University
Principal Investigator: Marc Moon, MD Washington University School of Medicine
Principal Investigator: William Chapman, MD Washington University School of Medicine
Principal Investigator: Ronald P Kaufman, MD Albany Medical College
Principal Investigator: Edward Chen, MD Emory University
Principal Investigator: Robin Kim, MD University of Utah
Principal Investigator: Derek DuBay, MD Medical University of South Carolina
Principal Investigator: Adam Yopp, MD University of Texas Southwestern Medical Center
Principal Investigator: Michael Argenziano, MD Columbia University
Principal Investigator: K. Scott Coffield, MD Baylor Scott and White Research Institute
Principal Investigator: Sean Castellucci, DO Manatee Medical Research Institute
Principal Investigator: Viraj Master, MD Emory University
Principal Investigator: Kiran Turaga, MD University of Chicago
Principal Investigator: Carlo B Ramirez, MD Thomas Jefferson University
Principal Investigator: Keith B Allen, MD St. Luke's Hospital
Principal Investigator: Elaine Tseng, MD San Francisco VA
Principal Investigator: Michael Jessen, MD University of Texas Southwestern Medical Center
Principal Investigator: Michael D'Angelica, MD Memorial Sloan Kettering Cancer Center
Principal Investigator: Jonathan Silberstein, MD, MPH Tulane University School of Medicine
Principal Investigator: S.Chris Malaisrie, MD Northwestern University
Principal Investigator: Charles St. Hill, MD University of Nevada, Las Vegas
Principal Investigator: Douglas Scherr, MD Weill Cornell Urology
Principal Investigator: Thomas Guzzo, MD University of Pennsylvania Perelman School of Medicine
Principal Investigator: Aaron Milbank, MD Minnesota Urology
CryoLife, Inc.
March 2018

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP