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Fat Grafting Technique for Fecal Incontinence

Primary Purpose

Fecal Incontinence

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Fat Grafting for Fecal Incontinence
Sponsored by
Melanie Salerno, RN
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fecal Incontinence

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age: >18 < 65 years
  2. Sex: females
  3. Affected by fecal incontinence (moderate to severe) independently from the etiology and previous treatments
  4. No restrictions to follow-up for 24 months after treatment
  5. Willing and able to provide informed consent

Exclusion Criteria:

  1. Present diagnosis of cancer (not in remission)
  2. Patients with uncorrected rectal prolapse
  3. Overflow incontinence
  4. Patients with neurogenic bowel or spinal cord injuries
  5. Any patients unable to give informed consent, including members of vulnerable populations
  6. Patients with concomitant pelvic floor disorders, like paradoxical puborectalis contraction or pelvic floor dysfunction
  7. Chronic diarrhea
  8. Patients with chronic steroid use
  9. Patients 17 and under
  10. Anal Sepsis (abscess and/or fistula)
  11. Inability to undergo the intended diagnostic tests and follow-up
  12. Pregnancy
  13. Diagnosis of Diabetes Mellitus 1 and 2

Sites / Locations

  • LifespanRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Patients with Fecal Incontinence

Arm Description

Patients will have the opportunity to undergo adipose tissue harvesting and targeted local Injection under ultrasound guidance in muscle defects in the intersphincteric space, all around the remaining portions of the external anal sphincter, and along the course of the pudendal nerves bilaterally

Outcomes

Primary Outcome Measures

Resolution of Fecal Incontinence Measured by patient reported outcomes on questionnaires
Comparison of pre and post procedure outcomes via outcomes questionaires
Resolution of Fecal Incontinence Measured by Physical Exam
Comparison of pre and post procedure outcomes via Endoanal Ultrasound and Physiology Testing

Secondary Outcome Measures

Incident of treatment related adverse events
Site reported adverse events designated as related to treatment

Full Information

First Posted
March 18, 2019
Last Updated
July 7, 2020
Sponsor
Melanie Salerno, RN
Collaborators
Lifespan
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1. Study Identification

Unique Protocol Identification Number
NCT03882632
Brief Title
Fat Grafting Technique for Fecal Incontinence
Official Title
Evaluation of Fat Grafting Technique Using Autologous Micro-fragmented Autologous Adipose Tissue Lipogems in Fecal Incontinence
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 11, 2019 (Actual)
Primary Completion Date
April 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Melanie Salerno, RN
Collaborators
Lifespan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Fecal Incontinence affects an estimated 2-20% of the general population, and up to 50% of the elderly and institutionalized population. Patients with incontinence tend to suffer in silence; they often do not seek help because of embarrassment and stigma. They often become confined to their homes because they are afraid of having an "accident". Although this is not a life-threatening condition, the psychological, emotional, and social impact can be devastating.
Detailed Description
The purpose of this study is to evaluate reconstructive lipoplasty with micro-fragmented autologous adipose tissue (Lipogems®) in female patients with fecal incontinence. Our hypothesis is that placing approximately up to 90 cc of Lipogems® will yield an effective increase in surviving material (over normal fat injection) due to the refinement of the process and result in decreased fecal incontinence over the long term. Human Adipose Tissue (Fat) possesses regenerative properties in its stromal vascular fraction (SVF). SVF contains nests of pericytes and human MSC mesenchymal stem cells). MSCs are multipotent cells (also called stromal multipotent cells), that possess the ability to differentiate into various tissues, such as bone, tendon, articular cartilage, ligaments, muscle, and fat. Upon fragmentation of adipose tissue using Lipogems®, viable elements are preserved with pericyte identity within an intact stromal vascular niche. It is hypothesized that upon trauma or disruption of this adipose tissue, the regenerative cells within the intact perivascular niche interact via micro vesicles with the microenvironment at the transplant site to promote angiogenesis, neuronal sprouting and fibroblast production thereby stimulating increased vasculature (circulation, nerve regeneration, muscle growth and tone in the urethral sphincter and in the urethral muscles). If these changes are observed, long lasting regenerative changes occur and should be long lasting versus the shorter live effects of the bulking effect by undisrupted fat tissue. This is a pilot study of 10 subjects will be treated with local injections of Lipogems® and followed for up to two years. Subjects will receive a full history and examination by a single colorectal surgeon. A clear history of their incontinence frequency, Wexner Incontinence Score, Fecal Incontinence Quality of Life Scale, surgical history, and childbirth history will be collected for all registered patients in order to categorize the study participant according to incontinence-type. All patients will undergo anal physiology testing and endoanal ultrasound. Pre and post measurements will be recorded and compared for objective evaluation. Patients will be evaluated subjectively with the Wexner incontinence Score and Fecal Incontinence Quality of Life Scale. Patients will have the opportunity to undergo adipose tissue harvesting and targeted local Injection under ultrasound guidance in muscle defects in the intersphincteric space, all around the remaining portions of the external anal sphincter, and along the course of the pudendal nerves bilaterally. This will be done in the procedure room or operating room with IV sedation and local anesthesia. This will all occur in the same setting on the same day.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fecal Incontinence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patients with Fecal Incontinence
Arm Type
Experimental
Arm Description
Patients will have the opportunity to undergo adipose tissue harvesting and targeted local Injection under ultrasound guidance in muscle defects in the intersphincteric space, all around the remaining portions of the external anal sphincter, and along the course of the pudendal nerves bilaterally
Intervention Type
Device
Intervention Name(s)
Fat Grafting for Fecal Incontinence
Other Intervention Name(s)
Fat Grafting
Intervention Description
Autologous adiopse tissue harvesting/grafting using Lipogems
Primary Outcome Measure Information:
Title
Resolution of Fecal Incontinence Measured by patient reported outcomes on questionnaires
Description
Comparison of pre and post procedure outcomes via outcomes questionaires
Time Frame
2 years
Title
Resolution of Fecal Incontinence Measured by Physical Exam
Description
Comparison of pre and post procedure outcomes via Endoanal Ultrasound and Physiology Testing
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Incident of treatment related adverse events
Description
Site reported adverse events designated as related to treatment
Time Frame
2 years

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Female Patients
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: >18 < 65 years Sex: females Affected by fecal incontinence (moderate to severe) independently from the etiology and previous treatments No restrictions to follow-up for 24 months after treatment Willing and able to provide informed consent Exclusion Criteria: Present diagnosis of cancer (not in remission) Patients with uncorrected rectal prolapse Overflow incontinence Patients with neurogenic bowel or spinal cord injuries Any patients unable to give informed consent, including members of vulnerable populations Patients with concomitant pelvic floor disorders, like paradoxical puborectalis contraction or pelvic floor dysfunction Chronic diarrhea Patients with chronic steroid use Patients 17 and under Anal Sepsis (abscess and/or fistula) Inability to undergo the intended diagnostic tests and follow-up Pregnancy Diagnosis of Diabetes Mellitus 1 and 2
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Melanie Salerno
Phone
4014447148
Email
melanie.salerno@brownphysicians.org
Facility Information:
Facility Name
Lifespan
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melanie Salerno, RN
Phone
401-444-7148
Email
melanie.salerno@brownphysicians.org
First Name & Middle Initial & Last Name & Degree
Leslie Roth, MD

12. IPD Sharing Statement

Learn more about this trial

Fat Grafting Technique for Fecal Incontinence

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