Pilot Study Evaluating the Efficacy of AlloMEM After Loop Ileostomy (AlloMem)
Primary Purpose
Colon Cancer, Rectal Cancer
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
AlloMEM™
Sponsored by
About this trial
This is an interventional prevention trial for Colon Cancer focused on measuring Ileostomy, Stenosis, Surgical Wound Dehiscence, Peritoneal, Colorectal Surgery
Eligibility Criteria
Inclusion Criteria:
- Between 18 - 85 years old at the time of ileostomy formation
- Scheduled to undergo planned diverting loop ileostomy
Exclusion Criteria:
- Patients undergoing emergency surgery
- Patients with abdominal or pelvic abscess present at time of initial surgery
- Patients with a history of pulmonary embolism or deep vein thrombosis (DVT) within 1 year of surgery
Sites / Locations
- University Hospitals Case Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Human Peritoneal Membrane: AlloMEM™
Arm Description
For use as a homologous tissue where native peritoneum is absent or traumatized. By decreasing adhesions and providing a peritoneal remodeling capacity, both the time needed for ileostomy closure and the risk of enterotomy or seromyotomy would be reduced. The combination could lead to decreased complication rates and therefore decreased morbidity for the surgical patients requiring an ileostomy.
Outcomes
Primary Outcome Measures
If there is a decrease on adhesion formation of AlloMEM™ used in formation of a temporary loop ileostomy.
Change in adhesion formation will be analyzed via the primary outcome of ileostomy mobilization time during ileostomy closure and the secondary outcome of an adhesion grading scale.
Secondary Outcome Measures
Decrease in operative time and a promotion of peritoneal remodeling
The objective of this study is therefore, to investigate whether the use of HPM in a temporary loop ileostomy is beneficial to patients. Benefit will be defined, for purposes of this study, as a decrease in adhesions resulting in decreased operative time during ileostomy closure, with promotion of peritoneal remodeling
Full Information
NCT ID
NCT01113736
First Posted
April 12, 2010
Last Updated
May 6, 2022
Sponsor
University Hospitals Cleveland Medical Center
Collaborators
Proxy Biomedical Limited
1. Study Identification
Unique Protocol Identification Number
NCT01113736
Brief Title
Pilot Study Evaluating the Efficacy of AlloMEM After Loop Ileostomy
Acronym
AlloMem
Official Title
Pilot Study Evaluating the Efficacy of AlloMEM in Prevention of Intraperitoneal Adhesions & Peritoneal Regeneration After Loop Ileostomy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospitals Cleveland Medical Center
Collaborators
Proxy Biomedical Limited
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The objective of this study is to investigate whether the use of Human Peritoneal Membrane (HPM) in a temporary loop ileostomy is beneficial to patients. Benefit will be defined, for purposes of this study, as a decrease in adhesions resulting in decreased operative time during ileostomy closure, with promotion of peritoneal remodeling.
Detailed Description
A loop ileostomy is a common procedure used to divert fecal matter from anastomotic sites after abdominal surgeries. Major complications from creation and subsequent closure of a temporary loop ileostomy include: stoma retraction, stoma prolapsed, stenosis, herniation, intra-abdominal abscess, anastomotic leak, wound dehiscence. Small-bowel obstruction (SBO) was the most common complication. SBO is caused by adhesions in the surgical site, with narrowing or angulation of the intestine causing obstruction. Prevention of these adhesions may reduce the frequency with which SBO is seen after this surgery. Furthermore, surgery to close the ileostomy is complicated by the presence of adhesions which make dissection of the ileostomy difficult, and increase the risk of injury of the small intestine during dissection, prolonging the operation time in an effort to minimize risk to the patient.
AlloMEM™ is human peritoneal membrane designated by the Food and Drug Administration (FDA) for use as a homologous tissue where native peritoneum is absent or traumatized. The AlloMem™ is not regulated as a device and no 510k submission has been made by the FDA. AlloMem™ is allogeneic freeze-dried, irradiated human peritoneal membrane used as a soft tissue wound covering solely regulated under 361 HCT/P because by FDA definition it is: minimally manipulated; intended for homologous use only; does not involve the combination of cell or other tissues, and does not rely on the metabolic function of cells for its primary function. Two animal studies have shown that AlloMEM™ can help prevent intra-abdominal adhesions and provides the biological framework for peritoneal remodeling. By decreasing adhesions and providing a peritoneal remodeling capacity, both the time needed for ileostomy closure and the risk of enterotomy or seromyotomy would be reduced. The combination could lead to decreased complication rates and therefore decreased morbidity for the surgical patients requiring an ileostomy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer, Rectal Cancer
Keywords
Ileostomy, Stenosis, Surgical Wound Dehiscence, Peritoneal, Colorectal Surgery
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Human Peritoneal Membrane: AlloMEM™
Arm Type
Experimental
Arm Description
For use as a homologous tissue where native peritoneum is absent or traumatized. By decreasing adhesions and providing a peritoneal remodeling capacity, both the time needed for ileostomy closure and the risk of enterotomy or seromyotomy would be reduced. The combination could lead to decreased complication rates and therefore decreased morbidity for the surgical patients requiring an ileostomy.
Intervention Type
Biological
Intervention Name(s)
AlloMEM™
Other Intervention Name(s)
Human Peritoneal Membrane
Intervention Description
To investigate whether the use of HPM in a temporary loop ileostomy is beneficial to patients.
Primary Outcome Measure Information:
Title
If there is a decrease on adhesion formation of AlloMEM™ used in formation of a temporary loop ileostomy.
Description
Change in adhesion formation will be analyzed via the primary outcome of ileostomy mobilization time during ileostomy closure and the secondary outcome of an adhesion grading scale.
Time Frame
Average 1 hour during formation of ileostomy
Secondary Outcome Measure Information:
Title
Decrease in operative time and a promotion of peritoneal remodeling
Description
The objective of this study is therefore, to investigate whether the use of HPM in a temporary loop ileostomy is beneficial to patients. Benefit will be defined, for purposes of this study, as a decrease in adhesions resulting in decreased operative time during ileostomy closure, with promotion of peritoneal remodeling
Time Frame
During 3 month ileostomy closure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Between 18 - 85 years old at the time of ileostomy formation
Scheduled to undergo planned diverting loop ileostomy
Exclusion Criteria:
Patients undergoing emergency surgery
Patients with abdominal or pelvic abscess present at time of initial surgery
Patients with a history of pulmonary embolism or deep vein thrombosis (DVT) within 1 year of surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Conor P. Delaney, MD, PhD
Organizational Affiliation
University Hospitals Cleveland Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospitals Case Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
19628227
Citation
Jin J, Voskerician G, Hunter SA, McGee MF, Cavazzola LT, Schomisch S, Harth K, Rosen MJ. Human peritoneal membrane controls adhesion formation and host tissue response following intra-abdominal placement in a porcine model. J Surg Res. 2009 Oct;156(2):297-304. doi: 10.1016/j.jss.2009.04.010. Epub 2009 May 13.
Results Reference
background
PubMed Identifier
23670746
Citation
Keller DS, Champagne BJ, Stein SL, Ermlich BO, Delaney CP. Pilot study evaluating the efficacy of AlloMEM for prevention of intraperitoneal adhesions and peritoneal regeneration after loop ileostomy. Surg Endosc. 2013 Oct;27(10):3891-6. doi: 10.1007/s00464-013-3004-6. Epub 2013 May 14.
Results Reference
derived
Learn more about this trial
Pilot Study Evaluating the Efficacy of AlloMEM After Loop Ileostomy
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