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NCT Number: NCT01674439

Clinical Trial of Fat Grafts Supplemented With Adipose-derived Regenerative Cells

Although first reports of the clinical use of adipose-derived regenerative cells (ADRC) suggest that this approach may be feasible and effective for soft tissue augmentation, there is a lack of randomized, controlled clinical trials in the literature. Hence, this study aimed to investigate whether a novel protocol for isolation of ADRC and their use in combination with fat tissue improve the long-term retention of the grafts in patients with craniofacial microsomia.

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Key information

Age range

10 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Division of Plastic and Reconstructive Surgery

São Paulo, 01246000, Brazil

About this study

To overcome problems associated with fat grafting, such as unpredictable clinical results and a low rate of graft survival, many innovative efforts and refinements of surgical techniques have been reported. For example, condensation of living tissue and removal of unnecessary components have been performed by centrifugation, filtration or gravity sedimentation; external mechanical force has been used to expand the recipient tissue as well as the overlying skin envelope; and a recent experimental study has suggested that repeated local injections of erythropoietin might enhance retention of grafted fat.

Based on the finding that aspirated fat tissue contains a much smaller number of adipose-derived regenerative cells (ADRC) compared with intact tissue and that these cells play pivotal roles in the adipose tissue remodeling after lipoinjection, the supplementation of fat grafts with stromal vascular fraction isolated from adipose portion of liposuction aspirates has been proposed as a method to compensate its relative deficiency of ADRC.

In the literature, there are at least three experimental studies demonstrating that supplementation of adipose progenitor cells enhances the volume or weight of surviving adipose tissue, and first reports of the clinical use of ADRC suggest that this approach may be feasible and effective for soft tissue augmentation.

However, since these studies represent level of evidence IV, which correspond to the publication of case series, there is a lack of randomized, controlled clinical trials comparing this method to current standard techniques.

Hence, this study aimed to fill this gap by investigating whether a novel protocol for isolation of ADRC and their use in combination with fat tissue improve the long-term retention of the grafts in patients with craniofacial microsomia.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Unilateral craniofacial microsomia
  • 10 to 35 years old
  • Phenotype (M0, M1 or M2) and (S1 or S2) according to the OMENS-PLUS classification

Exclusion criteria

  • Previous soft tissue surgery
  • Absence of fat donor site

Treatment and study plan

Supplementation of ADRC

Procedure

Isolation of ADRC from half of the aspirated fat and supplementation of the fat grafts with these cells

Other names: Cell-assisted lipotransfer

Without supplementation of ADRC

Procedure

Standard fat graft preparation

Other names: Structural fat grafting

Primary outcomes

  1. Graft volume retention

    Time frame: 6 months postoperative

    Graft volume retention evaluated by CT-scan performed at the preoperative period and at 6-months postoperative

Secondary outcomes

  1. Number of viable cells before and after the supplementation of the grafts

    Time frame: immediate postoperative

    Number of viable cells in adipose tissue evaluated by trypan blue method immediately after surgery

Sponsors and collaborators

Lead sponsor

University of Sao Paulo

Other

Registry information

Official study title

Randomized Controlled Clinical Trial of Fat Grafts Supplemented With Adipose-derived Regenerative Cells for Facial Soft Tissue Augmentation in Patients With Craniofacial Microsomia.

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Aug 28, 2012
Registry last updated
Aug 28, 2012

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.

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