Trials / Completed
CompletedNCT05850104
Comparison of Classical Prosthesis and Silicone Prosthesis
Comparison of Classical Prosthesis and Silicone Prosthesis in Patients With Chopart Amputation
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 24 (actual)
- Sponsor
- Gaziler Physical Medicine and Rehabilitation Education and Research Hospital · Academic / Other
- Sex
- Male
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to investigate the effects of classical Chopart prosthesis and silicone prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation.
Detailed description
The purpose of this study is to investigate the effects of classical Chopart prosthesis and silicone prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation. This study will be useful for prescribing the appropriate prosthesis in patients with Chopart amputation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | the effects of classical Chopart prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation. | the effects of classical Chopart prosthesis and silicone prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation. |
| OTHER | the effects of silicone prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation. | the effects of silicone prosthesis on socket comfort, satisfaction level and quality of life in patients with unilateral Chopart amputation. |
Timeline
- Start date
- 2023-05-24
- Primary completion
- 2023-11-24
- Completion
- 2023-11-24
- First posted
- 2023-05-09
- Last updated
- 2024-03-19
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT05850104. Inclusion in this directory is not an endorsement.