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Outcomes of the leg amputee of vascular origin welcomed in the hospital

Clinical outcomes of lower extremity amputees of vascular origin admitted to the hospital environment: randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10kch7gy
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-05-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amputation

Interventions

100 individuals in the immediate postoperative phase of lower extremity amputation at ICSC will participate in the study. Participants will be allocated into two groups: intervention group (GI) - perf
control group (CG) - the physiotherapeutic functional reception intervention will not be performed. Randomization will occur in chronological order of amputation, interspersing 5 individuals for each
SP2.157.108

Sponsors

Universidade do Estado de Santa Catarina
Lead Sponsor
Universidade do Estado de Santa Catarina
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Syme, boyd, pirigoff, chopart, stripe, transmetatarsal and finger disarticulation, both unilateral and bilateral, in the immediate postoperative period; amputation for vascular cause; both sexes; age 18 years or older

Exclusion criteria

Exclusion criteria: The intervention group will be adopted as exclusion criteria: individuals with hemodynamic instability

Design outcomes

Primary

MeasureTime frame
Presentation of the expected outcome to know the sociodemographic and clinical profile, based on the method of data collection in electronic medical records. We will observe the prevalence of the variables: sex; age; marital status; schooling; originating municipality; race and occupational status. Clinical information: total length of hospital stay (days); length of hospital stay to perform the amputation procedure; postoperative time to hospital discharge (days); reason for hospital admission; clinical diagnosis of hospitalization; associated comorbidities; pasta; stature; type of amputation; amputation laterality; smoking; alcoholism; practice of physical activity; use of walking aids. After selecting the data, the body mass index and its respective classification will be calculated according to the mass and height collected in the individual's medical record. From a descriptive analysis of the data, it will be possible to trace the clinical and sociodemographic profile of this individual.;Presentation of the expected outcome functional status through the application of the modified barthel index. Based on the modified barthel index, it is possible to assess activities of daily living, divided into ten categories: food; bathing, clothing, personal hygiene, intestinal eliminations, bladder eliminations, use of the toilet, chair-bed transfer, ambulation and stairs. For each item there are five response options, 1. dependent; 2. full assistance; 3. partial assistance; 4. minimal assistance; 5. independence. The classification is performed by scores that in the sum can vary from 0 to 100. The interpretation of the result is done through the cut-off points, as follows: 100 points - totally independent; 99 to 76 points - mild dependence; 75 to 51 points - moderate dependence; 50 to 26 points - severe dependence; 25 or less points - total dependence; values ??less than or equal to 20 points - increased probability of mortality.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactSoraia da Luz

Universidade do Estado de Santa Catarina

soraia.luz@udesc.br+55 (48) 3321-8670

Outcome results

None listed

Source: REBEC (via WHO ICTRP)