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Clinical Trials/NCT02635932
NCT02635932
Completed
Not Applicable

Effectiveness of Trapeziometacarpal Splint

Federal University of São Paulo1 site in 1 country60 target enrollmentStarted: January 2016Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Federal University of São Paulo
Enrollment
60
Locations
1
Primary Endpoint
Change in pain scale

Overview

Brief Summary

The trapeziometacarpal osteoarthritis is a degenerative or inflammatory joint that affects the trapeziometacarpal joint (TMC) of the thumb. Its main symptom is pain that leads to difficulty in manual function and decrease the patient's quality of life. Immobilization of TMC thumb joint by bracing has been effective in reducing pain and improving function. Objective: To compare the effectiveness between day and night functional splint for patients with trapeziometacarpal osteoarthritis in improving pain and function

Detailed Description

Randomized clinical trial, and blind where selected 60 patients diagnosed with trapeziometacarpal osteoarthritis.Os patients were assessed by a blinded evaluator at the beginning of treatment and after 45, 90 and 180 days in relation to pain, thumb range of motion, strength hold, tweezers, dexterity, function and satisfaction.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with osteoarthritis in accordance with the American College of Rheumatology classification criteria (ACR); of both genders and age above 18 years; Pain in TMC articulation between 3 and 8 cm in numerical pain scale (END) 10cm

Exclusion Criteria

  • Patients with severe deformities in hand with trapeziometacarpal osteoarthritis not possible to achieve pincer movement between the first, second and third fingers
  • Deformity of the distal interphalangeal joint (IFD) of the thumb
  • Use of splint the thumb in the last six months; Have surgery scheduled on hand for the next six months
  • Allergy to the material of the splint
  • Inability to respond to the questionnaire and perform the tests
  • Geographic inaccessibility
  • Infiltration in hand in the previous 3 months
  • Changes in the use of anti-inflammatory and analgesic past 3 months
  • Physiotherapy in hand over the last 3 months
  • Have the following related diseases: carpal tunnel syndrome, carpal fractures of DeQuervain syndrome, tendonitis, fibromyalgia and chronic inflammatory arthropathy.

Outcomes

Primary Outcomes

Change in pain scale

Time Frame: baseline, after 45, 90 and 180 days

Secondary Outcomes

  • Change in Functional capacity using the Cochin Hand Functional Scale questionnaire(baseline, after 45, 90 and 180 days)
  • Change in pinch and grip strength(baseline, after 45, 90 and 180 days)

Investigators

Sponsor
Federal University of São Paulo
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Fabiana de Carvalho Silva

Physiotherapist

Federal University of São Paulo

Study Sites (1)

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