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Polyneuropathies clinical trials

View clinical trials related to Polyneuropathies.

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NCT ID: NCT00507936 Completed - Clinical trials for Diabetic Neuropathies

Safety and Efficacy Study in Subjects With Diabetic Neuropathic Pain

Start date: August 2007
Phase: Phase 2
Study type: Interventional

This study will compare the efficacy and the safety of ABT-894 (1mg, 2mg or 4mg capsules) administered BID to placebo in the treatment of DNP. Another treatment arm will be Duloxetine 60mg administered once daily (QD). Approximately 275 subjects will be enrolled into the study at approximately 50 sites in both the United States and Europe. The study will be divided into the following periods: Screening/Washout (21 days) followed by a Baseline Visit, an 8-week Treatment Period and a 1-week Follow-up Visit.

NCT ID: NCT00501202 Completed - Clinical trials for Diabetic Polyneuropathy

Study for Safety and Effectiveness of RWJ-333369 (Carsibamate) for the Treatment of Diabetic Peripheral Neuropathy (DPN).

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety, effectiveness, and tolerability of 200 mg of RWJ-333369 given twice daily by mouth compared with placebo in the treatment of Diabetic Peripheral Neuropathy (DPN).

NCT ID: NCT00483730 Completed - Clinical trials for Symptomatic Diabetic Peripheral Polyneuropathy

Actovegin® Versus Placebo in Patients With Diabetic Polyneuropathy (AV-007-IM)

Start date: December 2006
Phase: Phase 3
Study type: Interventional

To assess clinical efficacy and safety of Actovegin in type 2 diabetic patients with symptomatic diabetic peripheral polyneuropathy after 250 ml i.v. infusions once daily for 20 days followed by oral treatment 600 mg × 3 daily for 140 days.

NCT ID: NCT00476931 Completed - Clinical trials for Diabetes Mellitus, Type 2

Clinical Trial of SB-509 in Subjects With Diabetic Neuropathy

Start date: May 2007
Phase: Phase 2
Study type: Interventional

The purpose of the study is to study the clinical effects of the investigational drug, SB-509 versus placebo in patients with diabetic neuropathy.

NCT ID: NCT00409175 Completed - Clinical trials for Familial Amyloid Polyneuropathy

Safety and Efficacy Study of Fx-1006A in Patients With Familial Amyloidosis

Start date: January 2007
Phase: Phase 2/Phase 3
Study type: Interventional

This study will examine whether Fx-1006A is effective in halting the progression of Familial Amyloid Polyneuropathy (FAP). Deposition of TTR amyloid is associated with a variety of human diseases. Deposition of amyloid fibrils of variant TTR (primarily V30M) in peripheral nerve tissue produces the condition called FAP. The prevention of the formation of amyloid by stabilization of the TTR native state should constitute an effective therapy for amyloid diseases. Therapeutic intervention with a TTR stabilizer drug, such as Fx-1006A, is hypothesized to stop progression of the disease in FAP patients. FAP is a uniformly fatal disease and Fx-1006A is intended to halt the relentless neurological deterioration FAP patients experience. This Phase 2/3 study will enroll early to mid-stage FAP patients in order to interrupt and stabilize the disease at a point in time where progression of motor and autonomic dysfunction can be maximally effected. Male and female patients with FAP with documented V30M TTR mutation will receive Fx-1006A or placebo once daily for a period of eighteen (18) months.

NCT ID: NCT00406458 Completed - Clinical trials for Diabetes Mellitus, Type 2

Clinical Trial of SB-509 in Subjects With Diabetic Neuropathy

Start date: November 2006
Phase: Phase 2
Study type: Interventional

The purpose of the study is to study the clinical effects of the investigational drug, SB-509 versus placebo in patients with diabetic neuropathy.

NCT ID: NCT00328601 Completed - Clinical trials for Diabetic Polyneuropathy

Assessment of Efficacy and Safety of Thioctic Acid in the Oral Treatment of Symptomatic Diabetic Neuropathy (SYDNEY 2)

Start date: February 2005
Phase: Phase 3
Study type: Interventional

The primary objective of the trial is to determine the optimal dose of orally (tablet) administered thioctic acid in the treatment of symptoms of diabetic polyneuropathy (dPNP). It is expected that at least one of the three dosages to be tested (600, 1200, or 1800 mg tablets) of orally administered thioctic acid improves the symptoms of dPNP as compared to placebo. Secondary objectives are evaluations of other variables pertinent to dPNP, safety, and tolerability.

NCT ID: NCT00307749 Completed - Clinical trials for Diabetic Polyneuropathy

Safety and Efficacy of MCC-257 in the Treatment of Diabetic Polyneuropathy

Start date: March 2006
Phase: Phase 2
Study type: Interventional

The primary objectives of the study are to evaluate the efficacy and safety of three doses of MCC-257 in patients with mild to moderate diabetic polyneuropathy

NCT ID: NCT00294671 Completed - Clinical trials for Familial Amyloid Polyneuropathy

The Effect of Diflunisal on Familial Amyloidosis

Start date: February 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if diflunisal can prevent progressive lower leg nerve damage in patients with familial amyloidosis polyneuropathy. Funding Source - FDA OOPD; NINDS

NCT ID: NCT00289497 Completed - Diabetes Clinical Trials

TempTouch IR Thermometry & Diabetic Patient Self-Care

Start date: June 2000
Phase: Phase 2/Phase 3
Study type: Interventional

Foot ulcers develop in diabetics with neuropathy because of cumulative injury over the course of several days. These patients do not feel pain, and do not recognize their foot is being injured until a wound develops. Areas about to ulcerate become inflamed and “hot spots” can be identified. This study’s purpose is to evaluate the effectiveness of a home infrared temperature probe designed to forewarn patients that an area on the foot is inflamed so they can take preventive measures. The study will evaluate the incidence of diabetic foot ulcers among high-risk patients, evaluate the cost of home temperature monitoring compared to standard therapy, and evaluate patient satisfaction. 180 diabetics at high-risk of having foot complications will be randomized into 3 treatment arms: 1) standard therapy consisting of regular foot care; 2) standard therapy plus recording of a structured foot evaluation using a hand mirror; and 3) standard therapy plus infrared home temperature assessment to identify “hot spots.” Device patients will measure temperatures at 6 sites on the foot each day. When temperatures are elevated >4°F patients will contact the research nurse and decrease activity. The primary study outcome will be incident foot ulcers and Charcot fractures.