search
Back to results

Lipomodelling for Symptomatic Peri-stomal Skin Contour Abnormalities: a Pilot and Feasibility Study (LiSPA)

Primary Purpose

Stoma

Status
Unknown status
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
Lipomodelling of symptomatic peri-stomal skin contour abnormalities
Sponsored by
Western Sussex Hospitals NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stoma focused on measuring Stoma, Peri-stomal, Lipomodelling

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients aged 18 - 100 years old
  • Patients who are able to give informed consent
  • Patients who have had a stoma (colostomy, ileostomy or urostomy) for > 1 year
  • Patients with a stoma that is likely to be permanent
  • Patients with a stoma that is not due to be reversed within the following year (length of study)
  • All patients with a stoma suffering with frequent soiling due to difficulty in stoma bag fitting will be assessed. If this is due to peri-stomal skin contour abnormalities they may be suitable for lipomodelling.
  • Preoperative assessment will be based on clinical history, clinical examination and inspection of peri-stomal area prior to registering as a participant for the trial.

Exclusion Criteria:

  • Patients unable to give informed consent or refuse to participate in this study
  • Patients who have had their stoma for less than 1 year
  • Patients with a temporary stoma that is due o be reversed within a year
  • Patients who have a stoma on which the stoma bag fits securely and is not leaking
  • Patients with allergy to any medication used in local infiltration
  • Patients with an underlying medical condition that excludes them from the study (e.g. risk of increase in bleeding such as patients on warfarin.)
  • Patients with evidence of underlying infection.

Sites / Locations

  • Worthing HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Lipomodelling

Arm Description

Lipomodelling of peri-stomal skin contour abnormalities

Outcomes

Primary Outcome Measures

Requirement for the use of extra stomal appliances
Extra appliances are usually required by patients who have stomas that constantly leak because the bag does not fit properly. After undergoing lipomodelling around the stoma the aim is for the stoma bag to fit more securely and less stoma appliances will be needed.
Quality of life
If the stoma bag is fitting more securely then an improvement in the patients quality of life is anticipated.

Secondary Outcome Measures

Frequency of soiling in 24 hours.
If the stoma bag fits more securely then there should be less soiling and leakage.
Cost analysis
If less extra stoma appliances are required then this may save money.

Full Information

First Posted
November 11, 2013
Last Updated
March 18, 2014
Sponsor
Western Sussex Hospitals NHS Trust
search

1. Study Identification

Unique Protocol Identification Number
NCT02090985
Brief Title
Lipomodelling for Symptomatic Peri-stomal Skin Contour Abnormalities: a Pilot and Feasibility Study
Acronym
LiSPA
Official Title
The Use of Lipomodelling Induced Skin Rejuvenation for the Management of Symptomatic Peri-stomal Skin Contour Abnormalities to Improve Quality of Life. A Pilot and Feasibility Study.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Unknown status
Study Start Date
September 2013 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
June 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Western Sussex Hospitals NHS Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study a technique called 'lipomodelling' is being studied to find out if it is beneficial around the stoma site in patients who have difficulty with securing their stoma bags which may lead to leakage and frequent soiling which we believe reduces quality of life. Patients with colostomy (stoma formed by bringing large bowel to the surface of the abdomen), ileostomy (small bowel) or a urostomy (urinary tract) will be recruited into this study. Lipomodelling is a technique that is commonly used elsewhere in the body but to our knowledge has not been used for this purpose. This study is a pilot study that may lead to further research in this area. Lipomodelling means taking some of your own fat that lies just beneath the surface of the skin and transferring it to another part of your body. The fat is removed by suction (liposuction), normally from your thighs or abdomen. In order to use the most important part of the fat, it is then put into a machine called a centrifuge. This spins the fat so that it splits up into three different sections. The most important section is then separated and injected in very small quantities into the required areas around your stoma. It is thought to have cells that encourage rejuvenation as well as helping to fill the area injected. Peri-stomal means the area around the stoma itself, this includes skin and underlying tissue, which will be fat and scar tissue. After any operation there will be scarring that takes some time to fully develop. Usually after a year the scar tissue will be fully formed. The scar tissue may cause the skin around the stoma to be irregular. This is described as contouring of the skin. The aim of this study is to see if lipomodelling can improve your quality of life by reducing the frequency of changing your stoma bag, reduce leakage and the need for extra-stomal appliances to try and help the stoma bag fit to your body securely.
Detailed Description
OBJECTIVE Symptomatic skin contour abnormalities often lead to frequent soiling and difficulty in stoma bag fitting. The objective of this study is to evaluate the effectiveness of peri-stomal lipomodelling in reducing the number of stoma bag changes in 24 hours and overall quality of life in this patient group. METHODS Patients will be identified by the stoma care nurses or digestive diseases or urology clinics. They will be assessed for suitability for the study. If suitable, informed consent will be taken. Quality of life questionnaires will be completed by the participant prior to the procedure and at several intervals following the procedure. Follow-up will end at 1 year post procedure. BACKGROUND Intestinal stoma formation for faecal diversion or defunctioning the bowel, is a commonly established procedure in colorectal surgical practice [1-6]. It can be performed by open as well by laparoscopic approach. However, placement of an ileoostomy or colostomy on the abdominal wall skin surface is associated with many skin complications like skin ulceration arising from excoriation and scarring, skin retraction leading to peri-stomal skin dimples and irregular margins [7-13]. This may result in the stoma appliance not fitting properly to the skin leading to frequent soiling of the skin and clothes. Soiling can cause a significant impact on the patients quality of life [14]. Soiling of the skin and clothes requires frequent change of stoma appliances, use of various fittings around stoma and under stoma bag to try to avoid soiling. Consequently, the cost of stoma management increases due to extra stoma care by stoma nurse and additional use of stoma appliances [15]. Stomas can be resited in order to try and improve the situation for the patient. This may require a major operation including a laparotomy (opening the abdomen). Due to previous surgery there is likely to be scar tissue inside the abdomen which can make this operation difficult and hazardous as there is a risk of damaging the bowel. This study aims to identify whether it is possible to reduce soiling by improving the area around the stoma so that the stoma bag can fit properly through lipomodelling. A technique that can be performed as a day case, under local anaesthetic and without a major operation. Lipomodelling, also known as autogenous fat transfer or fat transplantation, is used to correct skin deformities elsewhere (such as breast) and so may be useful in correcting peri-stomal skin deformities. We hypothesis that peri-stomal lipomodelling should improve the peri-stomal skin contour abnormality and therefore improve the fitting of the stoma bag to the skin so reduce soiling with the aim of reducing number of stoma bag changes in 24 hours and thereby improving quality of life. This technique has been applied to correct skin defects in patients undergoing breast surgery, limbs surgery, buttocks and genitals [16-19]. Recent studies demonstrated that adipose tissue harvested during lipomodelling is a very rich source of regenerative cells called adipose derived stem cells (ADSC) [20]. ADSCs are capable of self- renewal and also secrete growth factors [21]. ADSCs have been reported to enhance elasticity of scar tissue and promote healing in patients undergoing radiotherapy for breast cancer, and in complex Crohn's fistulae [22-26]. In the peri-stomal area hopefully the lipomodelling will not only fill the defect, but also improve the elasticity of the scar tissue softening the area. The objective of this prospective observational pilot study is to evaluate the effectiveness of peri-stomal lipomodelling in correcting the peri-stomal skin contour defects aiming to reduce the frequent of leakage and soiling, aiming to improve overall quality of life. Sample size: 20 patients for this phase 1 pilot study

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stoma
Keywords
Stoma, Peri-stomal, Lipomodelling

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lipomodelling
Arm Type
Experimental
Arm Description
Lipomodelling of peri-stomal skin contour abnormalities
Intervention Type
Procedure
Intervention Name(s)
Lipomodelling of symptomatic peri-stomal skin contour abnormalities
Primary Outcome Measure Information:
Title
Requirement for the use of extra stomal appliances
Description
Extra appliances are usually required by patients who have stomas that constantly leak because the bag does not fit properly. After undergoing lipomodelling around the stoma the aim is for the stoma bag to fit more securely and less stoma appliances will be needed.
Time Frame
Change is being assessed from pre and post procedure to end of follow-up at 12 months
Title
Quality of life
Description
If the stoma bag is fitting more securely then an improvement in the patients quality of life is anticipated.
Time Frame
Participants will be followed for 12 months following the procedure
Secondary Outcome Measure Information:
Title
Frequency of soiling in 24 hours.
Description
If the stoma bag fits more securely then there should be less soiling and leakage.
Time Frame
Participants will be followed for 12 months following the procedure
Title
Cost analysis
Description
If less extra stoma appliances are required then this may save money.
Time Frame
Participants will be followed for 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients aged 18 - 100 years old Patients who are able to give informed consent Patients who have had a stoma (colostomy, ileostomy or urostomy) for > 1 year Patients with a stoma that is likely to be permanent Patients with a stoma that is not due to be reversed within the following year (length of study) All patients with a stoma suffering with frequent soiling due to difficulty in stoma bag fitting will be assessed. If this is due to peri-stomal skin contour abnormalities they may be suitable for lipomodelling. Preoperative assessment will be based on clinical history, clinical examination and inspection of peri-stomal area prior to registering as a participant for the trial. Exclusion Criteria: Patients unable to give informed consent or refuse to participate in this study Patients who have had their stoma for less than 1 year Patients with a temporary stoma that is due o be reversed within a year Patients who have a stoma on which the stoma bag fits securely and is not leaking Patients with allergy to any medication used in local infiltration Patients with an underlying medical condition that excludes them from the study (e.g. risk of increase in bleeding such as patients on warfarin.) Patients with evidence of underlying infection.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anna Z Conway, MBBS
Phone
+44 7957 887394
Email
annaconway@doctors.org.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Riccardo Bonomi, MS
Phone
+44 1903 205111
Ext
85247
Email
riccardo.bonomi@wsht.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bonomi
Organizational Affiliation
Western Sussex Hospitals NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Worthing Hospital
City
Worthing
State/Province
East Sussex
ZIP/Postal Code
BN11 2DH
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anna Z Conway, MBBS, BSc, MRCS
First Name & Middle Initial & Last Name & Degree
Riccardo Bonomi, MS

12. IPD Sharing Statement

Learn more about this trial

Lipomodelling for Symptomatic Peri-stomal Skin Contour Abnormalities: a Pilot and Feasibility Study

We'll reach out to this number within 24 hrs