- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02500303
Influence of Diabetes on Lower Limb Amputation
Rehabilitation & Function Following Lower Limb Amputation: the Influence of Diabetes
Studieoversigt
Detaljeret beskrivelse
This research has been designed to ask the following question: What are the factors that influence the rehabilitation and functional outcomes following LEA, in the long term in both those with and without diabetes.
Therefore this study will be a prospective observational analysis of all those who undergo a LEA in one year within the Greater Glasgow & Clyde area with follow up at 6, 12 & 18 months from date of amputation.
- Primary Endpoint Comparison of rehabilitation and functional outcomes in those with diabetes to those without diabetes, up to 18 months post LEA.
Secondary endpoints
- At discharge from rehabilitation, the characteristics of those who proceed to limb fitting following LEA to those who do not will be defined.
- At discharge from rehabilitation, the characteristics of those with diabetes that do not proceed to limb fitting following LEA compared to those who do.
- At discharge from rehabilitation to 18 months post LEA, a comparison of the characteristics in those with and without diabetes.
- From six months post LEA, at 6 monthly intervals (6,12 & 18 months), a comparison of the health status, social circumstances, mobility and quality of life measures in those with and without diabetes.
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiesteder
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Glasgow, Det Forenede Kongerige, G11 6NT
- Western Infirmary
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Over 18 years of age with a major amputation above the ankle.
Exclusion Criteria:
- Amputation for tumour, trauma, congenital abnormalities
- Amputation at hip disarticulation or trans-pelvectomy level
- Adults with incapacity
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Mortality
Tidsramme: 3 years
|
Date of Death if applicable
|
3 years
|
|
Limb fitting
Tidsramme: 3 years
|
Dtae of receiving prosthetic limb
|
3 years
|
|
Length of stay
Tidsramme: 3 years
|
Length of time in hospital as an in patient
|
3 years
|
|
Readmission
Tidsramme: 3 years
|
Date of readmission to hospital
|
3 years
|
|
Further surgery
Tidsramme: 3 years
|
Number and level of further amputations
|
3 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
EQ-5D-5L
Tidsramme: 3 years
|
Quality of life measure
|
3 years
|
|
Reintegration to normal living index
Tidsramme: 3 years
|
3 years
|
|
|
Prosthetic Limb User Mobility
Tidsramme: 3 years
|
As assessed by the prosthetic limb user survey mobility scale
|
3 years
|
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Co-morbidities
Tidsramme: 3 years
|
Functional co-morbidity index
|
3 years
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Studieleder: Lorna Paul, PhD, University of Glasgow
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- GN13DI563
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