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The Effects of Two Different Orthosis on Pain, Hand Strength and Function in Patients With Thumb Carpometacarpal Osteoarthritis

NCT ID: NCT03327480

Last Updated: 2017-10-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-01

Study Completion Date

2018-11-01

Brief Summary

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The investigators aimed to assess the effects of two different hand orthosis on hand functioning, pain, disability and quality of life in patients with thumb osteoarthritis

Detailed Description

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The investigators will randomized 60 patients with stage 1 or 2 thumb osteoarthritis in two groups. The investigators will prescribe a neoprene CMC orthosis for patients in Group 1 and a thermoplastic CMC orthosis for patients in Group 2. The investigators will recommend these orthosis for six weeks. They will assess pain and disability before and after the treatment.

Conditions

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Osteoarthritis Thumb

Keywords

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osteoarthritis thumb orthosis functioning

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized controlled prospective trial
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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neoprene CMC orthosis

We will prescribe a neopren CMC orthosis for patients in Group 1 and a thermoplastic CMC orthosis for patients in Group 2

Group Type EXPERIMENTAL

orthosis

Intervention Type OTHER

Group 1: neoprebe CMC orthosis Group2: thermoplastic CMC orthosis

thermoplastic CMC orthosis

We will prescribe a neoprene CMC orthosis for patients in Group 1 and a thermoplastic CMC orthosis for patients in Group 2

Group Type EXPERIMENTAL

orthosis

Intervention Type OTHER

Group 1: neoprebe CMC orthosis Group2: thermoplastic CMC orthosis

Interventions

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orthosis

Group 1: neoprebe CMC orthosis Group2: thermoplastic CMC orthosis

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being aged between 18 and 70
* Grade 1 or 2 thumb osteoarthritis

Exclusion Criteria

* The other hand disorders such as fracture and carpal tunnel syndrome
* Previous hand surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Diskapi Teaching and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Aslı Can

medical doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Aslı Can

Identifier Type: -

Identifier Source: org_study_id