Clinical Trials Logo

Scleroderma clinical trials

View clinical trials related to Scleroderma.

Filter by:
  • Withdrawn  
  • Page 1

NCT ID: NCT04656704 Withdrawn - Scleroderma Clinical Trials

Hyaluronidase in Treating Oral Microstomia in Patients With Sclerosing Skin Disease

Start date: January 1, 2020
Phase: Early Phase 1
Study type: Interventional

The principal objective is to measure the degree to which oral microstomia caused by sclerosing skin disease improves after treating patients with local hyaluronidase injections. Investigator will determine improvements in oral aperture by measuring the centimeters of the height of oral opening. The secondary objectives are: Investigator will aim to assess changes in quality of life and functionality, by serial calculations of the Mouth Handicap in Systemic Sclerosis (MHISS). In addition, investigator would like to investigate how many treatments are required prior to treatment efficacy plateauing. Since there is minimal data on the use of hyaluronidase for oral microstomia, it is not yet clear how many treatments are ideally required for maximal effect. Patients will be brought in monthly for photographs, examination, assessment, and treatment. Our hypothesis is that hyaluronidase injections will significantly improve patients' ability to open their mouths and oral functionality. It remains unclear how many treatments will be required for maximal effect.

NCT ID: NCT03270722 Withdrawn - Dysphagia Clinical Trials

Functional Luminal Imaging Probe (FLIP) Topography Use in Patients With Scleroderma and Trouble Swallowing

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

FLIP topography has been FDA cleared to evaluate a variety of esophageal conditions, but has never been evaluated in patients with scleroderma. The investigators hope to evaluate this technology in patients who have scleroderma and various esophageal symptoms, and compare to non-scleroderma patients.

NCT ID: NCT02680717 Withdrawn - Scleroderma Clinical Trials

Comparative Effectiveness Trial in the Treatment of Pediatric Plaque Morphea

Start date: March 2016
Phase: Phase 1
Study type: Interventional

This is a study designed to evaluate the comparative effectiveness of topical medications for the treatment of circumscribed morphea.

NCT ID: NCT02588625 Withdrawn - Scleroderma Clinical Trials

A Double-Blinded Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986020 Versus Placebo in Diffuse Cutaneous Systemic Sclerosis (dcSSc)

Start date: February 2016
Phase: Phase 2
Study type: Interventional

This is a two part study. The purpose of Part A is to determine if BMS-986020 is effective in treatment of diffuse cutaneous systemic sclerosis using one dose of BMS-986020. The purpose of Part B is to determine if BMS-986020 is effective in treatment of diffuse cutaneous systemic sclerosis using two different doses of BMS-986020.

NCT ID: NCT02328625 Withdrawn - Scleroderma Clinical Trials

Scleroderma Treatment With Celution Processed ADRCs Registry

STAR
Start date: April 2015
Phase: N/A
Study type: Observational [Patient Registry]

This registry study will assess the safety and performance of the Celution Device in the processing of an autologous graft consisting of adipose derived regenerative cells (ADRCs) in the treatment of hand scleroderma.

NCT ID: NCT02166229 Withdrawn - Systemic Sclerosis Clinical Trials

Divalproex Sodium in the Treatment of the Cutaneous Manifestations of Scleroderma

Start date: June 2014
Phase: Phase 1/Phase 2
Study type: Interventional

To investigate the ability of divalproex sodium, a histone deacetylase inhibitor, to improve the digital manifestations of scleroderma including digital edema, calcinosis cutis, digital ulcers, and joint contractures.

NCT ID: NCT01639573 Withdrawn - Scleroderma Clinical Trials

Campath-1h Phase I/II Pilot Trial as Immunoablative Therapy for Refractory Systemic Sclerosis

CAMPATH-1H
Start date: April 2011
Phase:
Study type: Observational

This phase I/II pilot trial seeks to demonstrate that prolonged administration of Campath-1H without prior marrow or stem cell harvesting can result in immunoablation similar to that achieved by hematopoietic stem cell transplantation (HSCT) from either bone marrow or peripheral blood stem cell sources in children and adolescents with severe treatment refractory systemic sclerosis (SSc).

NCT ID: NCT01497743 Withdrawn - Scleroderma Clinical Trials

Probiotics in Patients With Moderate-to-severe Distention/ Bloating From Systemic Sclerosis

PRISS
Start date: February 2012
Phase: Phase 4
Study type: Interventional

Organs of the gastrointestinal tract include the mouth, throat, stomach, intestines, and anus. Patients with scleroderma often have GIT disorders. GIT disorders can be severely debilitating and even life-threatening. Some problems associated with GIT disorders may include heartburn, loss of voice or hoarseness, ulcers (open sores), difficulty swallowing, constipation, diarrhea, malabsorption (impaired absorption of nutrients from the GI tract), diminished peristalsis (decreased in the wavelike motion in the muscles of the intestines), and the inability to control your bowel movements. Probiotics are the "good bacteria" normally found in your digestive tract. Our group is looking at whether or not taking daily probiotics (lactobacillus) can help alleviate some of these symptoms in scleroderma patients that have GIT disorders.