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Clinical Trial Summary

The purpose of this research is to evaluate the safest and most effective dose of a Food and Drug Administration (FDA) approved drug (XIAFLEX) in the treatment of lipoma (fatty tumors of varying sizes that occur commonly in the adult population). The fat in the lipoma is like normal fat except that it is enclosed in a balloon-like structure which is made of collagen (fibrous tissue). Treatment of the lipoma with an injection of XIAFLEX (a protein that breaks down collagen fibers) may dissolve the collagen/fibrous strands thereby decreasing the size of the lipoma or removing it.


Clinical Trial Description

Lipomas are common mesenchymal, benign, fatty tumors of varying sizes that occur in the general adult population. They usually present as painful or annoying lumps that are palpable and often visible in the subcutaneous tissue. Many subcutaneous lipomas are asymptomatic and are removed for non-medical reasons. However, they may cause the subject pain or discomfort or interfere with normal activity.

Spontaneous remission of lipomas has not been reported. A lipoma, once it presents itself, remains there for the lifetime of a person who carries it and may stay small or become larger. Alternative treatments of the lipoma are surgery or liposuction. If a large excision is performed there is the problem of having a very large scar and the accompanying issues of healing a large scar, or possible formation of a hematoma followed by consolidation of the hematoma and the remnants of a mass of scar tissue. This is often painful and more problematic than the original lipoma. liposuction also has the potential for hematoma formation followed by scar mass residual.

To avoid the complications listed above, a non-invasive method of treatment, such as enzyme mediated disassociation of adipose tissue, would be desirable. The primary aim of this study is to perform a step-wise approach in dosing to evaluate the safety and efficacy of clostridium histolyticum as a non-operative treatment for lipoma. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01613313
Study type Interventional
Source Gerut, Zachary, M.D.
Contact
Status Completed
Phase Phase 2
Start date May 2012
Completion date October 2013

See also
  Status Clinical Trial Phase
Completed NCT00624416 - Association of Beta-2 Adrenergic Agonist and Corticosteroid Injection in the Treatment of Lipomas Phase 1/Phase 2
Completed NCT00608842 - Phase 2 Study for the Treatment of Superficial Lipomas Phase 2
Completed NCT00422188 - Deoxycholic Acid Injection for the Treatment of Superficial Lipomas Phase 1
Completed NCT03900078 - Incisional Negative Pressure Wound Therapy for Resection of Soft Tissue Tumors N/A
Completed NCT02249052 - Double Blind Study to Evaluate the Efficacy of Collagenase Histolyticum in the Treatment of Lipoma Phase 2