Novel Use of (Oral) Ketotifen for the Treatment of Fibromyalgia: A Pilot Study — KetoforFMS  

Fibromyalgia Clinical Trial

Official title: Novel Use of Ketotifen (Mast Cell Stabilizer) in Fibromyalgia: A Pilot Study

Status Active, not recruiting

Clinical Trial Summary

The purpose of this 10-week study is to determine the effects of a medication called Ketotifen on inflammation (blood) markers; pain sensitivity; and fibromyalgia-related pain.

Ketotifen works by inhibiting (to prevent or slow down) certain substances in the body that are known to cause inflammation. It is an antihistamine that reduces the harmful effects of histamine. The ophthalmic (eye drops) formulation of ketotifen has been approved by the Food and Drug Administration (FDA) and has been available in the United States for more than a decade. Oral (taken by mouth) ketotifen has been in available in other countries for several decades. Commonly prescribed for the maintenance treatment of asthma and allergic rhinitis, ketotifen has long track record of safety. To date, the oral form of ketotifen has not been approved by the FDA, therefore this study is referred to as an "investigational drug study." Prior to opening recruitment an "investigational new drug" (IND) application which included scientific data and information regarding human safety plans was submitted to and approved by the FDA.

Clinical Trial Description

Approximately 46 subjects will be participating in this research. Each subject will be randomized (like flipping a coin) to one of two groups; approximately 23 volunteers will be randomized to receive the active medication and 23 will receive the placebo. Both groups will be "blinded" (will not know) to which group they have been assigned.

The study will be conducted at the Indiana University Clinical Research Center for Pain (CRCP), located on the IUPUI campus in the National Institute of Fitness and Sport building,at 250 University Blvd.,Suite 118 Indianapolis, Indiana, 46202.

To summarize: The subject will be asked to visit the CRCP on four separate occasions:

Initial Screening, Week 1, Week 2, and Week 10. This study also includes, answering questionnaires, a blood samples drawn on two separate occasions, taking study medication, maintaining a written medication diary and agreeing to remain in weekly contact with the study team to answer a short side effect questionnaire. The side effect questionnaire will be conducted from week 1-4 and then once every 2 weeks from week 4-10.

Study Overview:

Week 0 (clinic visit 1):

1. Informed consent and initial screening questionnaire,

2. Review of all current medications

3. Light physical assessment, e.g. blood pressure, height, weight

4. The investigators will obtain a urine sample for a urine pregnancy test (UPT) and screening blood samples (approximately 17.5 ml /3.3 teaspoonfuls) from a vein in the subject's arm

5. Complete short thumb pressure testing in order to set the testing parameters for futures tests (week 1 and week 10)

6. Receive 'pain score' wrist monitor with instructions to record his/her pain level three times each day for one week

7. Receive a one-week medication packet along with instructions to take one tablet twice a day for seven days along with entering dosing information in a medication diary.

Week 1 (clinic visit 2):

1. Submit his/her pain score wrist monitor

2. Submit his/her medication diary for review and return any unused medication

3. Complete the self-assessment questionnaires via computer

4. Undergo a thumb pressures pain sensitivity test

5. If qualified to continue, the subject will receive the next 7-day supply of either a placebo or the active medication, ketotifen 1 mg. along with verbal and written instructions and a medication diary.

Week 2 (visit 3):

1. The investigators will assess the subject's willingness to continue study participation.

2. Review medication diary and medication side-effect/benefit checklist along with any unused study medication. If the subject has not experienced any bothersome side effect and agree to continue,he/she will be issued the next level of either the placebo or the active medication Ketotifen (2 mg.).

3. To assure the subjects' safety, the project coordinator or a member of the research team will complete a medication side-effect questionnaire. The subject will be asked to schedule a weekly check-in call for week 3 and 4 and once every 2 weeks from week 4 to week 10 (weeks 6, 8, and 10)

Week 10 (visit 4):

1. One week prior to this visit, the subject will receive a 'pain score' wrist monitor via an express delivery service (e.g., FedEx) and will be asked to enter his/her pain level three times a day for one week. Then return it during this visit.

2. Review medication side effect/benefit checklist, medication diary and return any unused medication.

3. Completion of self-assessment questionnaires via computer

4. Obtain exit blood samples (approximately 17.5 ml /3.3 teaspoonfuls) from a vein in his/her arm.

5. Undergo a thumb pressures pain sensitivity test. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Fibromyalgia
• Myofascial Pain Syndromes

• NCT number: NCT01553318
• Study type: Interventional
• Source: Indiana University
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: March 2012
• Completion date: March 2013