Osteoarthritis of the Small Joints of the Hand Clinical Trial
Official title:
Proof of Concept: Clinical Validation Study of Personalized Orthopedic Splints With 3D Technology in Patients With Rhizarthrosis
| NCT number | NCT04678622 |
| Other study ID # | BIOFERULA3D |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | July 27, 2018 |
| Est. completion date | December 31, 2018 |
| Verified date | December 2020 |
| Source | Optimus3D S.L. |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
Osteoarthritis of the hand is a chronic joint disease that usually affects one or more of the finger joints and it is a major cause of disability. Radiology and the Eaton-Littler classification (Stages I-II-III-IV) are used for its diagnosis. The treatment of stages I, II and in some cases of stage III, is based on pharmacological and rehabilitation measures, including the use of orthoses or splints. The development of Biosplint 3D will allow a qualitative leap forward in the search for an intelligent solution for patients with rhizarthrosis (Degenerative alteration of the trapezius-metacarpal joint (TMJ) characterized by a progressive deterioration of the articular surfaces and new bone formation in them). The aim of the study is to assess the feasibility of applying a personalized splint versus a conventional one. It is not a design aimed at evaluating the efficacy of such treatment. It is a prospective study with two arms, open with 1:1 allocation. The study includes a recruitment visit and two follow-up visits, one at a month and a final visit at 3 months. Patients with a new diagnosis of osteoarthritis of the trapeziometacarpal joint are included. One group of patients wears the usual splint indicated by the personalized doctors of the Service and the other group wears the 3D bi-splint. The main variable is pain, which will be measured by a visual analog scale (VAS). In addition, the DASH questionnaire (Disabilities of the Arm, Shoulder and Hand) and questions about patient satisfaction with the use of splints will be used.
| Status | Completed |
| Enrollment | 39 |
| Est. completion date | December 31, 2018 |
| Est. primary completion date | August 27, 2018 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 75 Years |
| Eligibility | Inclusion Criteria: - Clinical diagnosis of osteoarthritis of the trapeziometacarpal joint. - Radiological stage of Eaton-Littler classification I / II. - Patients in whom the placement of a discharge splint is clinically indicated. - Score between 3 and 7 on the VAS pain scale (range 0 to 10). Exclusion Criteria: - Previous treatment of osteoarthritis of the trapeziometacarpal joint. - Refuses to participate in the study. - Disabilities that prevent the completion of the questionnaires. - Presence of severe deformations in the hand. - Presence of other alterations, such as carpal tunnel syndrome, tendonitis or chronic inflammatory arthropathies. |
| Country | Name | City | State |
|---|---|---|---|
| Spain | Hospital Universitario Basurto | Bilbao | Vizcaya |
| Spain | Optimus 3D S.L. | Vitoria | Alava |
| Lead Sponsor | Collaborator |
|---|---|
| Optimus3D S.L. | Biocruces Bizkaia Health Research Institute |
Spain,
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | There are no relevant differences between the two orthoses in terms of fist force and clamp force. | By gripping force, using a dynamometer in the consultation. | It is performed at the second visit (one month after) and at the third follow-up visit (end of the study), which will take place at the third month of follow-up (between 11-14 weeks). | |
| Primary | Pain measured: Change of pain in patients with clasic orthrosis compared to the orthrosis designed using 3D technology | By visual analog scale from 0 (no pain) to 10 (unbereable pain) | Pain measurement by visual analog scale is performed at the baseline visit, at the second visit (one month later) and at the third follow-up visit (end of the study) which will take place at the third month of follow-up (between 11-14 weeks). | |
| Secondary | 3D orthoses change functionality | By DASH (10) scale consists of 30 items. In addition, there are 2 optional modules, with 4 items each one of them, that will measure the impact of an upper limb injury when playing musical instruments and when doing sports or working. Each item is scored from 1 to 5, with increasing values depending on the intensity of the symptoms. The score of the items is added to obtain a total score, which can range between 30 and 150 points and which is transformed into a scale from 0 (best possible score) to 100 (worst possible score).
The DASH scale makes it possible to assess the disability perceived by the patient to perform various activities, including activities of daily living and symptoms such as pain, stiffness or loss of strength. |
Functionality is performed at the baseline visit, at the second visit (one month after) and at the third follow-up visit (end of the study), which will take place at the third month of follow-up (between 11-14 weeks). | |
| Secondary | Satisfaction and compliance are equally superior in the 3D orthosis. | By satisfaction scale composed of 6 items (each of them scored from 0 to 10):
What is your level of satisfaction with the splint? Has the splint helped decrease your pain? Has the splint helped you maintain your daily activities? Has your quality of life improved? How comfortable was the use of the splint? How easy was it to follow the instructions for using the splint? |
Satisfaction is performed at the second visit (one month after) and at the third follow-up visit (end of the study), which will take place at the third month of follow-up (between 11-14 weeks). |