Pilot Study to Determine Effects of Salsalate in Type 1 Diabetes and Painful Peripheral Neuropathy

NCT ID: NCT01480297

Last Updated: 2015-04-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 8 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-11-30
• Study Completion Date: 2014-09-30

Brief Summary

This 12 week study will examine the effects of daily Salsalate treatment on markers of neuropathic pain and intra-epidermal nerve fiber density. the study is being done in people with type 1 diabetes with signs and symptoms of peripheral neuropathy.

Detailed Description

This project will be used to establish preliminary data for a planned NIH-sponsored multicenter study of the effects of salsalate on diabetic neuropathy (DN) in people with type 1 diabetes. Diabetic peripheral neuropathy (DN) ultimately affects one-half of the patients with type 1 diabetes (T1DM) and is a major cause of disability, high mortality, and poor quality of life. Although intensive glucose control has proven efficacy in delaying or preventing DN in T1DM and type 2 diabetes (T2DM), most people with diabetes do not reach and maintain glycemic levels needed to achieve these benefits. In addition, many patients with diabetes still develop diabetic complications, including DN, despite good glucose control. For DN, no disease modifying treatment other than glycemic control is available. Therefore, it is essential to identify new drug targets and to treat DN as early as possible in its course.

The investigators planned, multi-center study will be the first to determine the effect of an anti-inflammatory agent, salsalate, on DN development and progression, and on DN pain in type 1 diabetes. This proof-of-concept pilot study will measure the effects of short term (12 week) treatment with Salsalate on novel and on established measures of peripheral neuropathy. Ultimately, this may permit measurement of treatment effects over a shorter period of time than by using established measures such as nerve conduction studies. Salsalate, a prodrug form of salicylate, is used to treat osteoarthritis and other rheumatologic conditions. It is highly effective in modulating the IKKβ/NF-κB pathway, with a large margin of safety, and has a glucose lowering effect in patients with type 2 diabetes. The IKKβ/NF-κB pathway is unique in that it is implicated in both the pathogenesis of nerve fiber loss as well as pain in DN. The proposed study design employs a quantifiable early measure of DN, IENFD of the thigh, allowing for accurate assessment of actual nerve fiber density over time.

In the pilot study, biomarkers of pain found in IENF's as well as IENFD will be measured pre and post 3 months of treatment with Salsalate, 3 grams daily.

Conditions

Peripheral Neuropathy; Type 1 Diabetes

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Salsalate

All subjects will take Salsalate, 3 grams daily (as 3 divided doses of 1 gram with breakfast, lunch and dinner).

Group Type: EXPERIMENTAL

Salsalate

Intervention Type: DRUG

Salsalate 3 grams daily (1 gram TID with meals)

Interventions

Salsalate

Salsalate 3 grams daily (1 gram TID with meals)

Intervention Type: DRUG

Other Intervention Names

Salsalate (Amneal Pharmaceuticals)

Eligibility Criteria

Inclusion Criteria

• Type 1 diabetes (T1D)
• Peripheral neuropathy with symptoms of pain, or with other uncomfortable symptoms (e.g., burning, prickling).
• 18 to 70 years old
• Stable insulin treatment program for at least the past 3 months.
• Abnormal nerve conduction studies (based on study screening examination)
• Willing and able to take an oral (by mouth) medication 3 times per day for 3 months.
• WOMEN using an appropriate method of contraception during the course of the study (hormonal, IUD, or diaphragm.
• Willing and able to provide written informed consent for study participation.

Exclusion Criteria

• Neuropathy from a cause other than diabetes.
• Allergy to salsalate or similar medications (aspirin, non-steroidal anti-inflammatory medicines like ibuprofen and naproxen).
• Currently on blood thinning agents such as Coumadin, Heparin, Plavix, Pradaxa, high-dose aspirin (more than 325 mg daily).
• Any severe low blood sugar episodes in the past 6 months (needed assistance to treat).
• Diabetic ketoacidosis in the past 6 months.
• Severe neuropathy, or have had an ulcer or amputation on either foot or either leg.
• Creatinine level (a measure of kidney function is greater than 1.4 mg/dl (for women) or greater than 1.5 mg/dl (for men) or your estimated GFR is under 60.
• Albumin in your urine or other signs of reduced kidney function.
• Liver enzymes (including ALT, AST and Bilirubin) levels are more than 2 and ½ times the upper limit of normal.
• Blood platelets are less than 100,000 at the time of screening.
• Organ transplant (lung, kidney, heart, pancreas, liver).
• Chronic immunosuppressive therapy, for example, daily prednisone or other steroids, methotrexate, Imuran, CellCept. This includes daily, or recurrent use of oral steroids used to treat asthma.
• Regular NSAID medications (e.g., Naproxen, Ibuprofen) use. If used occasionally, you will be asked to not use them during the study.
• History of drug or alcohol abuse, or if you take more than 10 alcoholic drinks per week.
• History of stomach ulcers or bleeding from your bowel.
• Heart attack, heart bypass surgery, heart failure or a stroke EVER.
• Current treatment for any cancer (other than basal cell or squamous cell skin cancer).
• Treatment with lithium.
• Ever had Reyes' syndrome.
• Pregnant, nursing, or planning to become pregnant during the time of the study.
• Allergic to lidocaine or epinephrine (used for numbing skin prior to biopsies).
• Keloid scarring in the past.
• Receiving other experimental treatments.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Michigan

OTHER

Sponsor Role: lead

Responsible Party

Rodica Pop-Busui

Associate Professor of Internal Medicine

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Rodica Pop-Busui, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Michigan, Department of Internal Medicine

Locations

University of Michigan

Ann Arbor, Michigan, United States

Countries

United States

Other Identifiers

SALP

Identifier Type: -

Identifier Source: org_study_id