Histology and Ultrasound Pilot Study of HA Gels Adipose Tissue
Primary Purpose
Atrophy
Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Hyaluronic Acid filler
Hyaluronic Acid filler
Sponsored by
About this trial
This is an interventional basic science trial for Atrophy focused on measuring Hyaluronic Acid, histology, ultrasound, subcutaneous, adipose tissue
Eligibility Criteria
Inclusion Criteria:
- patients eligible for and requesting abdominoplasty
- patients eligible for and requesting bilateral breast reduction
Exclusion Criteria:
- Patients prone to hypertrophic scarring or keloids
- Hypersensitivity to hyaluronic acid
- Hypersensitivity to lidocaine or amide type local anaesthetics
- Autoimmune disease
- Severe, multiple allergies or anaphylactic shock
- Epilepsy
- Heart rhythm disorders
- Porphyria, congenital methemoglobinemia, glucose-6 phosphate dehydrogenase deficiencies, treatment with methaemoglobin-inducing substances.
- Previous streptococcal disease (acute rheumatic fever whether or not with heart valve involvement)
- Patients on medication which slows hepatic metabolism (such as cimetidine, beta-blockers)
- Diabetes requiring insulin treatment
- Major system disease.
- Coagulation disorders. Anticoagulation therapy. Chronic use of acetylsalicylic acid.
- Previous surgery in the areas eligible for injections.
- All contraindications to their surgical treatment (such as pregnancy or lactation).
Sites / Locations
- Universitair Ziekenhuis Brussel
- A.Z. Oudenaarde
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Hyaluronic Acid filler 1 for deep injection
Hyaluronic Acid filler 2 for deep injection
Arm Description
Injection Session 1 of Hyaluronic Acid filler 1, 3 weeks to 4 months before the surgery Injection Session 2 of Hyaluronic Acid filler 1, 5 to 9 days before the surgery
Injection Session 1 of Hyaluronic Acid filler 2, 3 weeks to 4 months before the surgery Injection Session 2 of Hyaluronic Acid filler 2, 5 to 9 days before the surgery
Outcomes
Primary Outcome Measures
tissue inflammation after injection of hyaluronic acid filler
Presence of lymphocytes and/ or histiocytes around the filler through histologic examination [Yes/No]
Secondary Outcome Measures
tissue response after injection of hyaluronic acid filler
Presence of lymphocytes and/ or histiocytes and/ or macrophages around the filler through histologic examination [Yes/No]
tissue response after injection and remodelling of hyaluronic acid filler
Presence of lymphocytes and/ or histiocytes and/ or macrophages around the filler through histologic examination [Yes/No]
tissue response after injection and remodelling of hyaluronic acid filler
Presence of lymphocytes and/ or histiocytes and/ or macrophages around the filler through histologic examination [Yes/No]
filler distribution in tissue
The height and width of the total filler spread [mm]
filler distribution in tissue
The height and width of the total filler spread [mm]
Full Information
NCT ID
NCT02868749
First Posted
July 27, 2016
Last Updated
January 22, 2019
Sponsor
Vandeputte, Joan, M.D.
Collaborators
Universitair Ziekenhuis Brussel
1. Study Identification
Unique Protocol Identification Number
NCT02868749
Brief Title
Histology and Ultrasound Pilot Study of HA Gels Adipose Tissue
Official Title
Comparative Clinical, Histological and Ultrasound Pilot Study of Two Hyaluronic Acid Gel Fillers, Designed for Deep Injection, in Adipose Tissue
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
March 22, 2017 (Actual)
Primary Completion Date
April 11, 2018 (Actual)
Study Completion Date
September 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vandeputte, Joan, M.D.
Collaborators
Universitair Ziekenhuis Brussel
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is a single-blind intra-individual comparative study to evaluate the short and medium term tissue response after the injection of 2 brands of hyaluronic acid gels (HA), designed for deep injection, that have been used for several years on a worldwide scale.
Detailed Description
The study will be disclosed to patients who present with an indication for either abdominoplasty or bilateral breast reduction with a Wise pattern skin excision (inverted T inframammary scar) Informed consent will be obtained from volunteers at their next consultation, during which the preoperative preparation is finalised and the surgery is booked.
Participants will receive injections for the first time three weeks to four months before the operation and for the second time five to nine days before the operation, in tissue that will be removed during the surgery.
In each session, through one single access point, a linear retrograde, subcutaneous injection will be performed with 0,5 ml of each of the studied hyaluronic acid gels, each in an opposite direction, each parallel to the skin surface.
Both sessions will be monitored by ultrasound examination. After the injections, the 2 cm of injected area which is most remote from the entrance point of the cannula will be remodelled by finger pressure and tissue pinching, to simulate remodelling as commonly performed after filler injection.
At the beginning of the operation, the injected subcutaneous fat will be removed with the overlying skin, to be sent for histologic examination.
The objective of the histologic examination is to assess the tissue response at one week versus three weeks to four months after the injection, as well as to assess the spread of the products, with and without remodelling after injection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrophy
Keywords
Hyaluronic Acid, histology, ultrasound, subcutaneous, adipose tissue
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hyaluronic Acid filler 1 for deep injection
Arm Type
Experimental
Arm Description
Injection Session 1 of Hyaluronic Acid filler 1, 3 weeks to 4 months before the surgery
Injection Session 2 of Hyaluronic Acid filler 1, 5 to 9 days before the surgery
Arm Title
Hyaluronic Acid filler 2 for deep injection
Arm Type
Active Comparator
Arm Description
Injection Session 1 of Hyaluronic Acid filler 2, 3 weeks to 4 months before the surgery
Injection Session 2 of Hyaluronic Acid filler 2, 5 to 9 days before the surgery
Intervention Type
Device
Intervention Name(s)
Hyaluronic Acid filler
Intervention Description
Linear retrograde, subcutaneous injection of 0,5 ml of hyaluronic acid gel in one side of the abdomen or one breast, 3 weeks to 4 months before the surgery.
Intervention Type
Device
Intervention Name(s)
Hyaluronic Acid filler
Intervention Description
Linear retrograde, subcutaneous injection of 0,5 ml of hyaluronic acid gel in other side of the abdomen or other breast, 5 to 9 days before the surgery.
Primary Outcome Measure Information:
Title
tissue inflammation after injection of hyaluronic acid filler
Description
Presence of lymphocytes and/ or histiocytes around the filler through histologic examination [Yes/No]
Time Frame
3 weeks to 4 months after injection
Secondary Outcome Measure Information:
Title
tissue response after injection of hyaluronic acid filler
Description
Presence of lymphocytes and/ or histiocytes and/ or macrophages around the filler through histologic examination [Yes/No]
Time Frame
1 week after injection
Title
tissue response after injection and remodelling of hyaluronic acid filler
Description
Presence of lymphocytes and/ or histiocytes and/ or macrophages around the filler through histologic examination [Yes/No]
Time Frame
3 weeks to 4 months after injection
Title
tissue response after injection and remodelling of hyaluronic acid filler
Description
Presence of lymphocytes and/ or histiocytes and/ or macrophages around the filler through histologic examination [Yes/No]
Time Frame
1 week after injection
Title
filler distribution in tissue
Description
The height and width of the total filler spread [mm]
Time Frame
3 weeks to 4 months after injection
Title
filler distribution in tissue
Description
The height and width of the total filler spread [mm]
Time Frame
1 week after injection
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
patients eligible for and requesting abdominoplasty
patients eligible for and requesting bilateral breast reduction
Exclusion Criteria:
Patients prone to hypertrophic scarring or keloids
Hypersensitivity to hyaluronic acid
Hypersensitivity to lidocaine or amide type local anaesthetics
Autoimmune disease
Severe, multiple allergies or anaphylactic shock
Epilepsy
Heart rhythm disorders
Porphyria, congenital methemoglobinemia, glucose-6 phosphate dehydrogenase deficiencies, treatment with methaemoglobin-inducing substances.
Previous streptococcal disease (acute rheumatic fever whether or not with heart valve involvement)
Patients on medication which slows hepatic metabolism (such as cimetidine, beta-blockers)
Diabetes requiring insulin treatment
Major system disease.
Coagulation disorders. Anticoagulation therapy. Chronic use of acetylsalicylic acid.
Previous surgery in the areas eligible for injections.
All contraindications to their surgical treatment (such as pregnancy or lactation).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joan H Vandeputte, MD
Organizational Affiliation
A.Z Oudenaarde (Oudenaarde General Hospital)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitair Ziekenhuis Brussel
City
Brussel
ZIP/Postal Code
B-1090
Country
Belgium
Facility Name
A.Z. Oudenaarde
City
Oudenaarde
ZIP/Postal Code
B-9700
Country
Belgium
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
pilot study on 5 patients: min, max, average measurements will be published
Citations:
PubMed Identifier
21272119
Citation
Flynn TC, Sarazin D, Bezzola A, Terrani C, Micheels P. Comparative histology of intradermal implantation of mono and biphasic hyaluronic acid fillers. Dermatol Surg. 2011 May;37(5):637-43. doi: 10.1111/j.1524-4725.2010.01852.x. Epub 2011 Jan 27.
Results Reference
background
PubMed Identifier
16485276
Citation
Hirsch RJ, Narurkar V, Carruthers J. Management of injected hyaluronic acid induced Tyndall effects. Lasers Surg Med. 2006 Mar;38(3):202-4. doi: 10.1002/lsm.20283.
Results Reference
background
PubMed Identifier
18547183
Citation
Arlette JP, Trotter MJ. Anatomic location of hyaluronic acid filler material injected into nasolabial fold: a histologic study. Dermatol Surg. 2008 Jun;34 Suppl 1:S56-62; discussion S62-3. doi: 10.1111/j.1524-4725.2008.34244.x.
Results Reference
background
PubMed Identifier
24077012
Citation
Micheels P, Sarazin D, Besse S, Sundaram H, Flynn TC. A blanching technique for intradermal injection of the hyaluronic acid Belotero. Plast Reconstr Surg. 2013 Oct;132(4 Suppl 2):59S-68S. doi: 10.1097/PRS.0b013e31829a02fb.
Results Reference
background
PubMed Identifier
26918965
Citation
Franca Wanick FB, Almeida Issa MC, Luiz RR, Soares Filho PJ, Olej B. Skin Remodeling Using Hyaluronic Acid Filler Injections in Photo-Aged Faces. Dermatol Surg. 2016 Mar;42(3):352-9. doi: 10.1097/DSS.0000000000000659.
Results Reference
background
PubMed Identifier
20048624
Citation
Shaw RB Jr, Katzel EB, Koltz PF, Kahn DM, Girotto JA, Langstein HN. Aging of the mandible and its aesthetic implications. Plast Reconstr Surg. 2010 Jan;125(1):332-342. doi: 10.1097/PRS.0b013e3181c2a685.
Results Reference
background
PubMed Identifier
17519724
Citation
Rohrich RJ, Pessa JE. The fat compartments of the face: anatomy and clinical implications for cosmetic surgery. Plast Reconstr Surg. 2007 Jun;119(7):2219-2227. doi: 10.1097/01.prs.0000265403.66886.54.
Results Reference
background
PubMed Identifier
24479675
Citation
Pilsl U, Rosmarin W, Anderhuber F. The premaxillary space: a location for filler injection? Dermatol Surg. 2014 Mar;40(3):301-4. doi: 10.1111/dsu.12431. Epub 2014 Jan 30.
Results Reference
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Histology and Ultrasound Pilot Study of HA Gels Adipose Tissue
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