A Study of Hyaluronan for the Treatment of Osteoarthritis in the Thumb

Phase 3

Completed

Conditions: Osteoarthritis

Interventions: Drug: Bupivicaine (local anesthesia injection)
Drug: Kenalog (triamcinolone; corticosteroid injection)
Drug: Synvisc (Hylan G-F20; hyaluronan injection)

Registration Number: NCT00398866

Lead Sponsor: Hospital for Special Surgery, New York

Brief Summary: Hyaluronan is a man-made preparation of a protein complex that occurs naturally in joints and that is often low in people with osteoarthritis. Although hyaluronan has been used in millions of people with knee osteoarthritis, it is not yet FDA approved for use in the thumb. The purpose of this study is to determine the safety and effectiveness of hyaluronan in relieving arthritis symptoms at the base of the thumb and to compare it to corticosteroids and local anesthetic.

The principle hypothesis is that treating osteoarthritis at the carpometacarpophalangeal (CMC) joint with injectable hyaluronan will results in greater pain relief, higher patient satisfaction, and better functional outcomes than treating with placebo injections (local anesthetic) or with corticosteroid injections. Treating CMC osteoarthritis with corticosteroid injections will result in greater pain relief, higher patient satisfaction, and better functional outcomes than treating with placebo injections. Patients with worse pre-treatment function will have less improvement and worse post-treatment results after administration of corticosteroid or hyaluronan.

Detailed Description: Osteoarthritis involves a wearing down of the cartilage within a joint. It can affect any joint in the body, but it most commonly affects joints in the hands, hips, knees, and spine. Over the last few years, a new medicine called hyaluronan has been used for treating osteoarthritis. Hyaluronan is a man-made preparation of a protein complex that occurs naturally in joints and that is often low in people with osteoarthritis. Although hyaluronan has been used in millions of people with knee osteoarthritis, it is not yet FDA approved for use in the thumb. The purpose of this study is to determine the safety and effectiveness of hyaluronan in relieving arthritis symptoms at the base of the thumb and to compare it to corticosteroids and local anesthetic. Specifically, the study will evaluate pain relief, patient satisfaction, and functional outcomes among participants.

Participation in this study will last 26 weeks. Screening will include a questionnaire and an x-ray of the affected thumb. Eligible participants will then be randomly assigned to one of three treatments: two hyaluronan injections, one corticosteroid injection plus one local anesthetic injection, or two local anesthetic injections. Participants will receive the injections at the base of their thumb, and the first injection will be followed by the second injection a week later. There will be five study visits that will occur at baseline and Weeks 2, 4, 12, and 26. All study visits will include questionnaires, and except for the Week 2 study visit, they will also include an examination and evaluation of the affected thumb. Photographs of the thumb will be taken at baseline. The injections will occur at baseline and Week 2. At Weeks 8 and 20, questionnaires will be mailed to participants for them to complete. Upon completing the study, participants will have the option of receiving continued treatment with another round of hyaluronic injections.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 200

Inclusion Criteria

Presence of osteophytes or sclerosis at the carpometacarpal (CMC) joint
Complaint of unacceptable pain despite modification of activity and a therapeutic dose of nonsteroidal anti-inflammatory drugs (NSAIDS), if tolerated
If bilateral disease, only the most severely involved hand (as defined by the visual analog scale [VAS] for pain) will be entered in the study
Able to follow instructions and complete questionnaires
Failed conservative therapy with NSAIDS or COX-2 inhibitors
Unable to tolerate COX-2 inhibitors

Exclusion Criteria

Previous traumatic dislocation, ligament tear, or fracture of the thumb in the affected hand
Previous hand surgery on the affected hand
Known hand comorbidities (e.g., active carpal tunnel syndrome, de Quervains tenosynovitis, etc.)
Systemic rheumatic disease
Bleeding diatheses or anti-coagulation
Allergies to steroids, chicken products, bupivicaine, or adhesive (e.g., double-sided tape)
Current use of oral or intravenous steroids
Active systemic malignancies
Hyaluronan injection in the target CMC joint in the last 6 months
Steroid or hyaluronan injection in any other joint in the last 6 months
Insulin dependent diabetes mellitus (IDDM)
Active infection
Pain in the index joint that is more than 40 out of 100 on a VAS Pain scale
End Stage CMC osteoarthritis, equivalent to bone on bone, Kellgren and Lawrence Stage IV
Grade 3 or 4 Eaton and Litter (E+L) Classification
E+L 3: Advanced joint distraction, subchondral cysts, and sclerosis
E+L 4: Involvement of several joint surfaces

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Bupivicaine (local anesthesia injection)	Bupivicaine (local anesthetic)
2	Kenalog (triamcinolone; corticosteroid injection)	Corticosteroid (trimcinolone (Kenalog) 40 mg)
3	Synvisc (Hylan G-F20; hyaluronan injection)	Synvisc

Primary Outcome Measures

Name	Time	Method
Pain Visual Analogue Scale (VAS)	Baseline, 26 Weeks	Pain intensity measured on a Visual Analog Scale with scores ranging from 0 to 100, with 100 = severe pain.

Secondary Outcome Measures

Name	Time	Method
Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire	Baseline, 26 Weeks	Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire measures degree of disability on a scale of 0 to 100, with a higher score indicating greater disability.