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Hand Orthosis for Hand Osteoarthritis
N/A
Waitlist Available
Led By Grace H Lo, MD MSc
Research Sponsored by Baylor College of Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 week follow up
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing two options for people with hand osteoarthritis. The goal is to reduce pain and prevent further damage to the hands. Participants will receive one of the options, both expected to be beneficial. The study will monitor their progress over several months.
Who is the study for?
This trial is for individuals with hand osteoarthritis who experience frequent pain in their fingers, have at least three affected joints, and are patients at the Michael E. DeBakey VA Medical Center in Houston, Texas. People planning or having had finger joint surgery, pregnant women, or those with inflammatory arthritis like gout or rheumatoid arthritis cannot participate.
What is being tested?
The study tests two different treatments for hand osteoarthritis to see which one might better alleviate pain and prevent further damage. Participants will be randomly assigned to one of these treatments without choosing which one they receive.
What are the potential side effects?
Since the intervention involves a hand orthosis (a type of brace), potential side effects may include discomfort from wearing the device, skin irritation under the brace, and possible restriction of movement leading to stiffness.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 week follow up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 week follow up
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
The primary structure endpoint will be change in sum of the Kellgren and Lawrence score of all Distal InterPhalangeal Joints in the hand that was placed in an orthosis over 24 weeks.
Visual analog scale (VAS) for pain in the more symptomatic hand that includes the most symptomatic DIP joint by 24 weeks of use of traction therapy with standard of care treatment for hand OA to establish efficacy of traction therapy.
Secondary study objectives
Functional Dexterity Test
Grip Strength
PinchStrength
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Treatment arm with experimental orthosisExperimental Treatment1 Intervention
Group II: Treatment arm with control orthosisActive Control1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
NSAIDs work by inhibiting cyclooxygenase (COX) enzymes, which are involved in the production of prostaglandins that cause inflammation and pain. By reducing prostaglandins, NSAIDs help alleviate pain and decrease inflammation in osteoarthritis (OA) patients.
Corticosteroid injections reduce inflammation by suppressing the immune response, inhibiting multiple inflammatory pathways, and thereby decreasing swelling and pain in the affected joints. Understanding these mechanisms is crucial for OA patients as it helps them and their healthcare providers make informed decisions about managing symptoms and improving quality of life.
Comparative effectiveness of pharmacologic interventions for knee osteoarthritis: a systematic review and network meta-analysis.Pathophysiology and first-line treatment of osteoarthritis.
Comparative effectiveness of pharmacologic interventions for knee osteoarthritis: a systematic review and network meta-analysis.Pathophysiology and first-line treatment of osteoarthritis.
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Who is running the clinical trial?
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)NIH
495 Previous Clinical Trials
1,089,459 Total Patients Enrolled
51 Trials studying Osteoarthritis
47,003 Patients Enrolled for Osteoarthritis
Baylor College of MedicineLead Sponsor
1,022 Previous Clinical Trials
6,029,387 Total Patients Enrolled
3 Trials studying Osteoarthritis
414 Patients Enrolled for Osteoarthritis
Grace H Lo, MD MScPrincipal InvestigatorBaylor College of Medicine
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Your pain level must be at least 40 out of 100 on a pain scale.You have had surgery on your fingertips.You have experienced pain most days of the month for at least one month over the past year.You are pregnant.You experience frequent and severe pain in at least one finger joint (DIP).You have at least 3 joints affected by distal interphalangeal (DIP) nodal hand OA.Heberden's nodes are present on physical exam.You are enrolled to receive medical care at the Michael EYou have a history of or currently have inflammatory joint conditions like gout, psoriatic arthritis, or rheumatoid arthritis.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment arm with control orthosis
- Group 2: Treatment arm with experimental orthosis
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Osteoarthritis Patient Testimony for trial: Trial Name: NCT04784065 — N/A
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