- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06439459
Skin Dermal Regeneration After Stromal Vascular Fraction Transplantation (SDR-SVF)
Quantitative Measurements of the Skin Dermal Regeneration After Stromal Vascular Fraction Transplantation
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is a prospective, exploratory investigation aimed at exploring the efficacy of stromal vascular fraction (SVF) transplantation in treating exhaustion of dermal regenerative capacity during skin expansion. The dermal thickness, texture, and perfusion before and after SVF transplantation would be recorded and analyzed by a series of quantitative devices including laser 3D scanner, Doppler ultrasound, VISIA skin analyzer, CK skin analyzer, and indocyanine green angiography.
The trial aims to include patients experiencing dermal exhaustion during the process of skin soft tissue expansion. We will extract SVF components from autologous adipose tissue and injected intradermally into the expanded skin. The changes of dermis of expanded skin were recorded before the treatment (baseline), and at 4 weeks and 8 weeks follow-up timepoints after SVF transplantation. More specifically, skin surface area was measured using laser 3D scan; skin thickness and texture were detected by Doppler ultrasound, VISIA skin analyzer and CK skin analyzer; skin blood perfusion was analyzed using indocyanine green angiography.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Huangpu
-
Shanghai, Huangpu, China, 200011
- Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- had undergone tissue expansion treatment;
- show signs of deterioration of skin texture during expansion, including stretch marks or thinning of the dermis (<2mm) with no improvement after suspending expansion for 2 weeks;
- require further expansion to achieve the size for defect reconstruction.
Exclusion Criteria:
- Patients with serious underlying diseases such as cardiovascular or cerebrovascular disease, peripheral vascular disease, or impaired liver or kidney function;
- Patients with a long history of smoking and alcohol use who have not quit smoking or drinking;
- Patients allergic to iodine or iodine-containing preparations;
- Patients with psychiatric disorders, lack of insight, or those who cannot accurately express themselves or cooperate;
- Patients with contraindications for SVF transplantation, such as ulceration or infection of the expanded skin;
- Patients with severely loose skin or insufficient subcutaneous fat tissue;
- Patients who request to withdraw informed consent and exit the clinical trial.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Stromal vascular fraction transplantation
Subcutaneous fat was harvested from either the abdomen or the posterior inner thigh region and then digested with 600 U of collagenase (Shanghai Qiaoyuan Biological Pharmaceutical Co., Ltd, Shanghai, China) at 37°C and 150rpm for three hours. After enzymatic digestion, the lower aqueous phase liquid was aspirated to acquire the stromal vascular fraction (SVF). The SVF cell-pellet was washed and adjusted to 2×10^6 cells/mL. The skin was marked with methylene blue and a total of 0.5ml (around 1×10^6 cells) were transplanted intradermally at the center of each 2cm×2cm squares. The expander was inflated two times a week using constant pressure inflation method, where the intracapsular pressure was monitored using a pressure meter and the inflation was halted when the pressure reached 100 mmHg. This procedure was repeated until adequate skin area was achieved for subsequent facial restoration surgery. |
Stromal vascular fraction was extracted from subcutaneous fat harvested from either the abdomen or the posterior inner thigh region. The SVF cell-pellet was washed and was adjusted to 2×10^6 cells/mL. The skin was marked with methylene blue and a total of 0.5ml (around 1×10^6 cells) were transplanted intradermally at the center of each 2cm×2cm squares. The expander was inflated two times a week using constant pressure inflation method, where the intracapsular pressure was monitored using a pressure meter and the inflation was halted when the pressure reached 100 mmHg. This procedure was repeated until adequate skin area was achieved for subsequent facial restoration surgery. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dermal thickness
Time Frame: Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Using Doppler ultrasound to measure the full-thickness of skin dermis of the expanded skin.
The measurements were conducted at the center of the expanded skin and other four points (above, below, left, right) around the center.
The average value is taken to represent the dermal thickness of the patient's expanded skin.
|
Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skin surface area
Time Frame: Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Using the HSCAN771 handheld laser 3D scanner and the VIVID910 3D laser scanning system to measure the surface area of the expanded skin.
|
Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skin texture (dermal rupture)
Time Frame: Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Using the VISIA skin analyzer to visualize the distribution of dermal marks, which is an indication of dermal rupture.
Briefly, photographs of the patient's expanded skin were taken from three standard angles: front, left side, and right side.
Use the VISIA instrument to generate texture imaging of the expanded skin, selecting the expanded skin and surrounding normal skin as the region of interest.
Employ the instrument's built-in red area analysis function to analyze the distribution of dermal marks in the expanded skin.
|
Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
|
Skin texture (elasticity)
Time Frame: Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Using the elasticity probe (Cutometer® MPA 580) of CK Skin analyzer to measure the elasticity of the expanded skin.
Represent skin softness through the skin viscoelasticity parameter R2 (R2 = Ua/Uf, where Ua is the total elastic and plastic recovery, and Uf is the total elastic and plastic deformation).
An R2 value closer to 1 indicates better skin elasticity.
The measurements were conducted at the center of the expanded skin and other four points (above, below, left, right) around the center.
Each point is measured three times, and the average value is taken to represent the measurement for that point.
|
Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
|
Skin perfusion
Time Frame: Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Indocyanine green (ICG) angiography was used to detect the blood perfusion of the expanded skin.
Briefly, the detector of SPY imaging system was adjusted to approximately 20 cm from the surface of the flap.
A white light photograph of the expanded skin was taken.
Without changing the detector position, indocyanine green imaging was performed as follows: Inject 2 ml of ICG solution (2.5 mg/ml) intravenously and fluorescence signals from the expanded skin were collected by SPY imaging system.
The integrated SPY-Q software was used for the analysis of the arterial and venous perfusion of the expanded flap.
|
Baseline: before SVF transplantation (Baseline); Follow-up: 4 and 8 weeks after SVF transplantation
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Shanghai9th-SDR-SVF-ZT
- 22MC1940300 (Other Grant/Funding Number: Science and Technology Commission of Shanghai Municipality)
- shslczdzk00901 (Other Grant/Funding Number: Shanghai Municipal Key Clinical Specialty)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Skin Regeneration
-
Shanghai Ninth People's Hospital Affiliated to...Not yet recruiting
-
Nanjing First Hospital, Nanjing Medical UniversityRecruitingLaser | Exosome | Skin RegenerationChina
-
Shanghai Jiao Tong University School of MedicineUnknownTissue Expansion; | Skin Regeneration; | Reconstruction; | Bone Marrow Mononuclear CellsChina
-
Future University in EgyptCompleted
-
Universidad Complutense de MadridCompletedBone Regeneration
-
Aesculap AGRecruitingBone RegenerationSpain
-
Dr R Viswa ChandraRecruiting
-
Institute of Liver and Biliary Sciences, IndiaCompletedLiver RegenerationIndia
-
Saint-Joseph UniversityUnknownBone RegenerationLebanon
Clinical Trials on Stromal vascular fraction transplantation
-
AntriaCompleted
-
Robert W Alexander, MDRegeneris Medical; Global Alliance for Regenerative MedicineUnknownOsteoarthritis | Back Pain | Tendinopathy | Tendinosis | Degenerative Joint Disease | Rheumatoid NoduleUnited States
-
Kasiak Research Pvt. Ltd.UnknownCritical Limb IschemiaIndia
-
Sohag UniversityNot yet recruitingAndrogenic Alopecia
-
Xijing HospitalRecruiting
-
Esbjerg Hospital - University Hospital of Southern...Odense University HospitalCompleted
-
Mayo ClinicWithdrawnBronchoesophageal Fistula | Tracheoesophageal Fistula | Tracheoesopharyngeal FistulaUnited States
-
Assistance Publique Hopitaux De MarseilleCompleted
-
Istituto Ortopedico RizzoliCompletedTendinopathy | Patellar Tendinopathy | Patellar TendinitisItaly