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Safety Of Fat Micrografts With Adipose-Derived Stromal Vascular Fraction In Hands Of Patients With Systemic Sclerosis

Phase 2
Completed
Conditions
Systemic Sclerosis
Interventions
Drug: ADSVF application in the right hand
Registration Number
NCT04387825
Lead Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Brief Summary

Systemic sclerosis (SS) causes microvascular alteration in the hand and subsequently pain, skin fibrosis, and osteoarticular deformities. These injuries initiate functional decline of the hand and decrease patient quality of life.

Local application of adipose-derived stromal vascular fraction (ADSVF) has been proposed as an emerging treatment. There are reports about the good results obtained after ADSVF treatment in this kind of patients. For these reasons , we aimed to evaluate the safety and clinical effect of application of fat micrografts enriched with ADSVF to the hands of patients with SS.

Detailed Description

The regenerative properties of adipose stem cells (ASCs) existing in the mixed cell fraction obtained by enzymatic digestion of adipose tissue, termed adipose-derived stromal vascular fraction (ADSVF), were initially described in 2002. These cells have the characteristics of being multipotent and exerting local angiogenic, anti-inflammatory, antifibrotic, immunomodulatory, and regenerative effects after application. ASCs express their angiogenic properties most effectively in a hypoxic environment.

For the above reasons, and because of its abundance in fat, easy acquisition, and almost immediate availability for use, ADSVF has positioned itself as an alternative for repair and regeneration of ischemic tissue.

Application of decanted fat, centrifuged fat, and ADSVF, has consistently and significantly improved pain, Raynaund Phenomen, and healing of digital ulcers in the hands of patients with SS, and thus improved their quality of life. Other inconsistent benefits have also been reported, such as decreased digital circumference, improvement in digital mobility and strength, improvement in formation of new subungual capillaries, and improvement in function through evaluation of the Cochin scale.

Based on the above findings, and because changes in the hands of patients with SS may arise through loss of adipocytes and defective stem cell function, we designed the present study with the aim of evaluating the safety, reproducibility, and clinical effects of application of fat micrografts enriched with ADSVF to the hands of patients affected with SS in a controlled clinical trial.

The experimental and control groups each contained 10 patients diagnosed with SS according to the criteria of the American College of Rheumatology and the LeRoy-Medsger criteria.

It was decided to carry out the treatment on the most affected hand of the patients, which was the right hand in the entire experimental group. ADSVF-enriched fat micrografts were applied to the experimental group. Evolution and medical therapy effects were observed in the control group.

The fat was obtained by liposucction and the ADSVF was processed in laboratory.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Patients diagnosed with SS, according to the criteria of the American College of Rheumatology and those of LeRoy-Medsger.
  • Over 18 years old,
  • BMI> 18 kg / m2.
  • Patients received stable vasoactive and immunosuppressive therapies, for at least 1 month before being enrolled in the study, and this was continued unchanged throughout the study.
Exclusion Criteria
  • infected digital ulcers
  • comorbidities that could affect hand function
  • alcoholism
  • drug abuse
  • history of family cancer
  • Patients with hyperbaric therapy one month before
  • Botulinum toxin one month before
  • surgical sympathectomy one month before

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental groupADSVF application in the right hand40 ml of fat was mixed with 2 ml of ADSVF and placed in 1-ml and 3-ml syringes. Using a 19-gauge blunt cannula (0.8 mm), 0.5 ml was applied to the radial and ulnar edge of each metacarpal phalangeal (MP) and interphalangeal (IP) joint in contact with each neurovascular digital pedicle and 3 ml was applied to each side of the metacarpal trapezius joint, together with 10 ml distributed subcutaneously throughout the palm of the hand and 10 ml evenly distributed on the back of the hand
Primary Outcome Measures
NameTimeMethod
Pain before the treatment and every day during one week after the treatment, and each 28 days after de first week until the 168 day168 days

Evaluation with Numerical Pain Rating Scale(NPRS) before, and after the intervention. The minimum value is 0 and maximum is 10. High value is worst

Frequency of Raynaud Phenomenon168 days

Frequency, number of events per day/week;

Duration of Raynaud Phenomenon168 days

Duration of minutes in every event.

Secondary Outcome Measures
NameTimeMethod
Digital Total active Motion168 days

Goniometry, kapandjy Test

Digital oximetry168 days

Transcutaneous Oximetry

Digital Ulcers168 days

Number of ulcers

Health status and disability index168 days

Evaluated by Sclerosis Health assessment Questionnarie (SHAQ) scale, before and at the end of the study. The value are from 0 to 3. A result \>1.25 is worst

Hand Function168 days

Cochin Scale, the values are from 0 to 90, higher values means poor function

Health-related quality of life, before de treatment and at the end of the study168 days

Short Form 36 (SF-36) scale. High values is poor patient health

Skin affection of the hand168 days

Modified Rodnan scale, the values are from 0 to 51. High values higher skin fibrosis

Vascularity of the nail bed168 days

Videocapillaroscopy by field

Trial Locations

Locations (1)

Instituto Nacional de Ciencias Medicas y Nutricion salvador Zubiran

🇲🇽

Mexico, Mexico

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