Demonstrate the Effectiveness to Hemopatch in Controlling Postoperative Bleeding After Laparoscopic Cholecistectomy and in Reducing of Morbidity and Postoperative Hospital Stay
Primary Purpose
Efficacy of Hemopatch in Controlling of Postoperative Bleeding or Reducing of Postperative Morbidity After Laparoscopic Cholecistectomy
Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Hemopatch Sealing Hemostat
Sponsored by
About this trial
This is an interventional prevention trial for Efficacy of Hemopatch in Controlling of Postoperative Bleeding or Reducing of Postperative Morbidity After Laparoscopic Cholecistectomy focused on measuring Laparoscopic, Cholecistectomy, Collection, Bleeding, reoperation
Eligibility Criteria
Inclusion Criteria:
- Gallbladder stone
- Polyp/neoplasm of gallbladder
Exclusion Criteria:
- Coagulopathies,
- Medication with antiplatelet agents
- ASA > 3
- Acute cholecystitis
- Main biliaru duct stone
- Acute pancreatitis
Sites / Locations
- Regina Apostolorum Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Hemopatch Sealing Hemostat
No Hemopatch Sealing Hemostat
Arm Description
Outcomes
Primary Outcome Measures
significant reduction in postoperative hospital stay
Secondary Outcome Measures
reducing of subhepatic volume drainage
reducing of liver hematoma
reducing of postoperative complications
reducing of rates of reoperation
reducing of re-hospitalization
To assess postoperative pain by the VAS scale 1-10.
Full Information
NCT ID
NCT02777307
First Posted
May 17, 2016
Last Updated
May 18, 2016
Sponsor
Ospedale Regina Apostolorum
Collaborators
Azienda Ospedaliera San Gerardo di Monza, San Giuseppe Moscati Hospital, Ospedali Riuniti di Foggia
1. Study Identification
Unique Protocol Identification Number
NCT02777307
Brief Title
Demonstrate the Effectiveness to Hemopatch in Controlling Postoperative Bleeding After Laparoscopic Cholecistectomy and in Reducing of Morbidity and Postoperative Hospital Stay
Official Title
Efficacy of Hemopatch in Reducing of Postoperative Bleeding After Laparoscopic Cholecystectomy: Prosective and Multicenter Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
June 2016 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
May 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ospedale Regina Apostolorum
Collaborators
Azienda Ospedaliera San Gerardo di Monza, San Giuseppe Moscati Hospital, Ospedali Riuniti di Foggia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Demonstrate the effectiveness to Hemopatch in controlling postoperative bleeding or reducing of postperative fluid collection after laparoscopic cholecistectomy, morbidity and postoperative hospital stay.
Detailed Description
Prospective Multicenter Longitudinal and cohort. The sample size of 150 patients was calculated in order to obtain a statistical power adequacy or higher (Type I error - Alpha = 0.05, Type II Error - Beta = 0:20), assuming the 1-day to reduce the postoperative stay with use Hemopatch compared to the control (average stay little 3 +/- 2 days).
Primary endpoint:
- significant reduction in postoperative hospital stay
Secondary endpoints:
reduction of subhepatic blood liquid volume
reduction of liver hematoma
reduction of postooperative complications as deep surgical site
reduction rates of reoperation
reduction in readmission rates
postoperative pain on the VAS scale 1-10.
The results obtained in relation to primary and secondary objectives will be compared with a control group of case-matched.
Inclusion Criteria:
- Between the ages of 18-75 years, calculus of gallbladder (micro- and macro-lithiasis), polyp/neoplasm of gallbladder
Exclusion Criteria:
- Coagulopathies, medication with antiplatelet drugs, ASA > 3, acute cholecystitis, simultaneous calculus of main biliary duct, acute pancreatitis.
The patient will enroll if cholecystectomy is performed laparoscopically, if it is not a complication occurred intraoperative type: iatrogenic enterotomy suture intestinal, iatrogenic lesion of liver parenchyma, bile duct injury. The patient will exclude from the study if one of these intraoperative complication will occur. The patient leaves the protocol if the dissection is done through energy-devices (ultrasound or radiofrequency).
At the end of the laparoscopic cholecstectomy, Hemopatch will be inserted into the peritoneal cavity through the port of 10-12 mm and laid on the cavity of the gallbladder and a drainage will be systematically placed.
It will be given a first-generation cephalosporin antibiotic (one shot).
At 24 hours of VLC a liver ultrasound will be performed and recorded: evaluation of presence of perihepatic fluid, collection or haematoma. It will be noted the volume of drainage which will be removed in first postoperative day. In case of delay removal of drainage, it will be recorded. It will be assessed postoperative pain by VAS scales to 6-12-24 h after surgery. Re-operations and re-hospitalizations will be recorded in prospective data.
Statistical analyzes were performed using the software SPSS for Mac, 22nd edition (SPSS Software, Inc., IL, Chicago). The differences in the distributions will be calculated using the chi-square test or Fisher exact test, depending on the number of cases in the various subgroups and by comparing means (Student t-test, one-way ANOVA test).
The p < 0.1 will be used as the cut-off for statistical significance in the selection of variables of multivariate analysis in order not to drop important potential predictors.
The statistical significance is conventionally defined with p <0.05 in all cases considered.
All eligible patients will be adequately informed and informed consent will be signed. The Study will be conducted according to ethical requirements, following the Declaration of Helsinki, and good clinical practice.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Efficacy of Hemopatch in Controlling of Postoperative Bleeding or Reducing of Postperative Morbidity After Laparoscopic Cholecistectomy
Keywords
Laparoscopic, Cholecistectomy, Collection, Bleeding, reoperation
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Hemopatch Sealing Hemostat
Arm Type
Experimental
Arm Title
No Hemopatch Sealing Hemostat
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Hemopatch Sealing Hemostat
Intervention Description
Place of Hemopatch Sealing Hemostat after laparoscopic cholecistectomy
Primary Outcome Measure Information:
Title
significant reduction in postoperative hospital stay
Time Frame
1 year
Secondary Outcome Measure Information:
Title
reducing of subhepatic volume drainage
Time Frame
1 year
Title
reducing of liver hematoma
Time Frame
1 year
Title
reducing of postoperative complications
Time Frame
1 year
Title
reducing of rates of reoperation
Time Frame
1 year
Title
reducing of re-hospitalization
Time Frame
1 year
Title
To assess postoperative pain by the VAS scale 1-10.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Gallbladder stone
Polyp/neoplasm of gallbladder
Exclusion Criteria:
Coagulopathies,
Medication with antiplatelet agents
ASA > 3
Acute cholecystitis
Main biliaru duct stone
Acute pancreatitis
Facility Information:
Facility Name
Regina Apostolorum Hospital
City
Albano Laziale
State/Province
Rome
ZIP/Postal Code
00041
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea Liverani, MD
Phone
+39693298501
Email
aliverani@reginaapostolorum.it
12. IPD Sharing Statement
Citations:
PubMed Identifier
24729905
Citation
Lewis KM, McKee J, Schiviz A, Bauer A, Wolfsegger M, Goppelt A. Randomized, controlled comparison of advanced hemostatic pads in hepatic surgical models. ISRN Surg. 2014 Mar 4;2014:930803. doi: 10.1155/2014/930803. eCollection 2014.
Results Reference
result
PubMed Identifier
25085811
Citation
Lewis KM, Spazierer D, Slezak P, Baumgartner B, Regenbogen J, Gulle H. Swelling, sealing, and hemostatic ability of a novel biomaterial: A polyethylene glycol-coated collagen pad. J Biomater Appl. 2014 Nov;29(5):780-8. doi: 10.1177/0885328214545500. Epub 2014 Aug 1.
Results Reference
result
PubMed Identifier
25239500
Citation
Imkamp F, Tolkach Y, Wolters M, Jutzi S, Kramer M, Herrmann T. Initial experiences with the Hemopatch(R) as a hemostatic agent in zero-ischemia partial nephrectomy. World J Urol. 2015 Oct;33(10):1527-34. doi: 10.1007/s00345-014-1404-4. Epub 2014 Sep 20.
Results Reference
result
PubMed Identifier
25106082
Citation
Lewis KM, Schiviz A, Hedrich HC, Regenbogen J, Goppelt A. Hemostatic efficacy of a novel, PEG-coated collagen pad in clinically relevant animal models. Int J Surg. 2014;12(9):940-4. doi: 10.1016/j.ijsu.2014.07.017. Epub 2014 Aug 6.
Results Reference
result
PubMed Identifier
21627788
Citation
Stokes ME, Ye X, Shah M, Mercaldi K, Reynolds MW, Rupnow MF, Hammond J. Impact of bleeding-related complications and/or blood product transfusions on hospital costs in inpatient surgical patients. BMC Health Serv Res. 2011 May 31;11:135. doi: 10.1186/1472-6963-11-135.
Results Reference
result
PubMed Identifier
20004553
Citation
Keus F, Wetterslev J, Gluud C, Gooszen HG, van Laarhoven CJ. Trial sequential analyses of meta-analyses of complications in laparoscopic vs. small-incision cholecystectomy: more randomized patients are needed. J Clin Epidemiol. 2010 Mar;63(3):246-56. doi: 10.1016/j.jclinepi.2009.08.023. Epub 2009 Dec 11.
Results Reference
result
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Demonstrate the Effectiveness to Hemopatch in Controlling Postoperative Bleeding After Laparoscopic Cholecistectomy and in Reducing of Morbidity and Postoperative Hospital Stay
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