Skip to main content
OpenTrials
Completed

NCT Number: NCT04387825

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Instituto Nacional de Ciencias Medicas y Nutricion salvador Zubiran

México, 14080, Mexico

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

ADSVF application in the right hand

Drug

40 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

Other names: Medical treatment

Primary outcomes

  1. Pain before the treatment and every day during one week after the treatment, and each 28 days after de first week until the 168 day

    Time frame: 168 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

  2. Frequency of Raynaud Phenomenon

    Time frame: 168 days

    Frequency, number of events per day/week;

  3. Duration of Raynaud Phenomenon

    Time frame: 168 days

    Duration of minutes in every event.

Secondary outcomes

  1. Digital Total active Motion

    Time frame: 168 days

    Goniometry, kapandjy Test

  2. Digital oximetry

    Time frame: 168 days

    Transcutaneous Oximetry

  3. Digital Ulcers

    Time frame: 168 days

    Number of ulcers

  4. Health status and disability index

    Time frame: 168 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

  5. Hand Function

    Time frame: 168 days

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

  6. Health-related quality of life, before de treatment and at the end of the study

    Time frame: 168 days

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

  7. Vascularity of the nail bed

    Time frame: 168 days

    Videocapillaroscopy by field

  8. Skin affection of the hand

    Time frame: 168 days

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

Sponsors and collaborators

Lead sponsor

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Other

Collaborators

  • National Council of Science and Technology, Mexico

Registry information

Official study title

Lipograft Safety Enriched With Vascular Stromal Fraction Derived From Adipose Tissue, to Treatment of Digital Joint Fibrosis and Refractory Ischemic Digital Ulcers Caused by Systemic Sclerosis

Important dates

Study start
2015
Primary completion
2019
Study completion
2020
First posted
May 14, 2020
Registry last updated
May 15, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.