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Lipoma clinical trials

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NCT ID: NCT05351164 Active, not recruiting - Clinical trials for Lipomatosis, Multiple Symmetrical

Evaluation of Safety and Efficiency of Metreleptin Treatment for Patients With Multiple Symmetric Lipomatosis (MSL)

Start date: August 1, 2023
Phase: Phase 2
Study type: Interventional

Patients (homozygous MFN2 [gene that provides instructions to produce the Mitofusin 2 protein] R707W) will be treated with Metreleptin, and effects on body composition, metabolic parameters and safety will be assessed over a 6 month intervention period. Additional safety will be assessed for 1 more year (up to 1.5 years total) in which adverse event data will be collected.

NCT ID: NCT04821583 Not yet recruiting - Clinical trials for Symmetric Lipomatoses, Multiple

Hydrocortisone Treatment for Symmetric Lipomatosis Associated With Neuropathy (SLN): an N-of-1 Study Hydrocortisone Treatment for Symmetric Lipomatosis Associated With Neuropathy (SLN): an N-of-1 Study

N-of-1 SLN
Start date: June 1, 2021
Phase: Phase 3
Study type: Interventional

A young women with Symmetric Lipomatosis associated with Neuropathy (SLN) was seen at the department of Internal Medicine - Endocrinology and at the department of Neurology at the Erasmus MC, Rotterdam, the Netherlands. The patient presented with balance problems due to neuropathy and prominent cervical and genital lipomas. In the past, the patient had been treated with steroids for a short period. The patient noticed that, as a 'side effect', during this treatment period the lipomas shrank and that the balance problems nearly disappeared. The complaints reappeared after withdrawal of the steroids. In the current study, the usefulness of steroid treatment in this single patient will be investigated in an N-of-1 trial. Primary objective: to determine the efficacy of hydrocortisone treatment for neuropathy on an individual level in a patient with SLN as assessed with the Rasch-built Overall Disability Scale (RODS).

NCT ID: NCT04236700 Recruiting - Labial Lipoma Clinical Trials

Buccal Evaluation of Mobile Beach Workers

Start date: November 22, 2019
Phase:
Study type: Observational

Tumors in the oral region occur more frequently in men over 40, but can affect people of both gender and all ages, even children. The prevention of oral cancer acquires relevance in public health, particularly if the investigators consider that the preventive approach is compatible with the nature of this disease, as the mouth favors easy visual access. The objective of this study is evaluation the prevalence of oral and perioral injuries in workers who were exposed to the sun on the beaches, investigating possible associations of a sociodemographic, occupational and general health nature.

NCT ID: NCT04229030 Completed - Clinical trials for Dercum's Disease Lipomas

RZL-012 for Dercum's Disease Lipomas

Start date: July 30, 2020
Phase: Phase 2
Study type: Interventional

Thirty-eight (38) subjects will be included in the study. Subjects will be randomized in a ration of 1:1 to be treated with RZL-012 or placebo. Subjects will be injected with a different doses of RZL-012 according to their lipomas sizes. The total of 38 subjects will be enrolled in 3 clinical sites.

NCT ID: NCT03900078 Completed - Soft Tissue Sarcoma Clinical Trials

Incisional Negative Pressure Wound Therapy for Resection of Soft Tissue Tumors

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

This study is aimed to examine the value of incisional negative pressure therapy after resection of soft tissue tumors. Its a prospective randomized trial comparing incisional negative pressure to standard wound dressings.

NCT ID: NCT02753361 Completed - Lipomas Clinical Trials

Ultra-sounded Guided Regional Blockade for Lipoma Excision

Start date: May 2016
Phase: N/A
Study type: Interventional

There is limited information on using the ultrasonography for block placement concerning lipoma excision. A new type of regional blockade, performed under ultrasound, can ensure proper block placement with accurate local anesthetics deposition. Investigators hypothesized that ultrasound guidance can reduce the number of needle passes to complete the block placement. Investigators will compare namely ultrasound guided regional blockade and traditional method regarding the number of needle passes to complete the block placement.

NCT ID: NCT02722681 Recruiting - Clinical trials for Lipoma of Spinal Cord

Developing a Biomarker for Monitoring Clinical Outcomes in Children With Spinal Lipoma.

Start date: February 2016
Phase: N/A
Study type: Observational

'Spinal lipoma' is a condition, present from before birth, in which fatty tissue (lipoma) is attached to the lower end of the spinal cord, tethering it within the vertebral canal. The cord normally moves up and down with respiration, whereas tethering prevents this movement, and can lead to progressive neurological deterioration. The cord and spinal nerves become stretched and their blood supply is damaged irreversibly. Disability may include weakness or pain in the lower body, and urinary disorders in young children. Treatment is surgical, to remove the lipoma and mobilise the spinal cord, with 60 such operations performed per year at Great Ormond Street Hospital. This project aims to develop lipidomic biomarkers in order to predict which children with spinal lipoma are at highest risk of neurological deterioration, and require early surgery, while providing evidence to adopt a more conservative approach for those at lower risk.

NCT ID: NCT02249052 Completed - Lipoma Clinical Trials

Double Blind Study to Evaluate the Efficacy of Collagenase Histolyticum in the Treatment of Lipoma

Start date: August 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether collagenase is effective in reducing the surface area of a subcutaneous benign lipoma.

NCT ID: NCT01613313 Completed - Lipoma Clinical Trials

A Dose Escalation Study Using Collagenase Clostridium Histolyticum in the Treatment of Lipoma

Start date: May 2012
Phase: Phase 2
Study type: Interventional

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.

NCT ID: NCT00624416 Completed - Lipoma Clinical Trials

Association of Beta-2 Adrenergic Agonist and Corticosteroid Injection in the Treatment of Lipomas

Start date: October 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test whether injected medications will increase the amount of fat released by a fat cell. We will compare prednisolone (a synthetic cortisone) combined with isoproterenol (a drug given for asthma) versus using isoproterenol alone. We will also test if injections of isoproterenol and prednisolone will shrink the size of lipomas, which are benign fatty tumors.