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Early Treatment of Post-stroke Spasticity With Botulinum Toxin (BTX_ST-ITA14)

21 de mayo de 2020 actualizado por: Nicola Smania, MD, Clinical Professor, Universita di Verona

Role of Early Treatment With Botulinum Toxin in Adult Patients With Post-stroke Spasticity: an Observational Multicenter Study

This was a multicentric observational study with the aim to evaluate the effect of early treatment with botulinum toxin type A (BoNT-A) on post-stroke spasticity in adult patients. All patients enrolled (86 patients) after a baseline clinical assessment (modified Ashworth scale, motricity index, Fughl Meyer assessment and modified Rankin' scale) undergoes to a BoNT-A injection following the evidence-based clinical practice. Subsequently, at 4, 12 and 24 weeks they underwent the same clinical evaluation as a follow-up. Results are under statistical evaluation.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Descripción detallada

This was a multicentric observational study with the aim to evaluate the effect of early treatment with botulinum toxin type A (BoNT-A) on post-stroke spasticity in adult patients. All centres involved are in Italy. The inclusion and exclusion criteria are described in detail in the correspondent section. The main outcome measure was to assess how the time elapsed from the acute event can influence the effectiveness of the focal treatment of spasticity with BoNT-A in adult patients with cerebral stroke. Secondary outcomes were to evaluate the spasticity' grade and the level of functioning using a clinical assessment (modified Ashworth scale, motricity index, Fughl Meyer assessment, Modified Rankin' scale).

The patients were enrolled from 10 centres that agreed to participate in this study (Azienda Ospedaliera Universitaria Integrata of Verona - coordinating centre; Azienda Ospedaliero Universitaria Ospedali Riuniti of Foggia; Azienda Ospedaliero-Universitaria of Ferrara; Azienda Ospedaliero-Universitaria Pisana; Azienda Ospedaliero Universitaria "Maggiore della Carità" of Novara; Azienda Ospedaliera Universitaria - Ospedali Riuniti of Ancona; Azienda Ospedaliera "Cardinale G. Panico" of Tricase; Fondazione Santa Lucia IRCCS of Rome; Azienda Ospedaliero-Universitaria Sant'Andrea of Rome; Ospedale "Ca' Foncello" of Treviso). No patients were enrolled from the last two centers that have expressed their waiver to participate when the study was already started.

Each patient (whether hospitalized or outpatient) included in the study underwent to a baseline evaluation in which near and remote pathological history were recorded (main concomitant pathologies, drug therapy in progress, previous major surgery, date of the stroke) and the following evaluation scales were administered: modified Ashworth scale (MAS), MI (motricity index), FMA (Fughl Meyer assessment) and Modified Rankin' scale (MRS). After that received a BoNT-A injection to treat the spasticity focally following the evidence-based clinical practice.

Each patient subsequently performed a follow-up evaluation at 4, 12 and 24 weeks after the date of inoculation through the execution of a specialist visit (physiatric/neurological) and the administration of the following evaluation scales: MAS, MI, FMA and MRS. For the duration of the study, each patient may undergo integrated rehabilitation treatment at the discretion of each of the investigators of each centre involved in the study according to the guidelines and common clinical practice.

The estimation of the sample size was hypothesized with the aim to observe a frequency of 75% in the number of patients who will show a reduction of one point at the MAS. If there is a correlation between the time elapsed since the acute event and the reduction in the degree of spastic hypertonia after the first administration of BoNT-A, to obtain an OR = 0.5, assuming DS = 1 and R2 = 0, with α = 0.05 and β = 0.20 (study power = 80%), 90 patients will be needed. Assuming a drop-out rate of 10%, a total of 100 patients will need to be enrolled in the study.

Descriptive statistics were produced (frequency histograms; position or central trend indices: average, median; variability or sample dispersion indices: standard deviation, interquartile range; sample distribution profile estimate: Shapiro-Wilk test; construction of the intervals of confidence) as regards demographic (age, gender, the time elapsed from a stroke) and clinical (MAS, MI, FMA and MRS score at baseline, 4, 12 and 24 weeks after BoNT-A injection).

In order to evaluate the role of the time elapsed from the acute event on the therapeutic efficacy of the first administration of BoNT-A 4 weeks after the inoculation (primary endpoint), a logistic regression analysis was performed in order to evaluate the effects of time since the acute event (independent variable) on the reduction of spastic hypertonia defined in dichotomous terms (dependent variable): RESPONDER (patient who will have obtained a reduction of at least 1 point in MAS of the degree of spastic hypertonia after 4 weeks from the administration) and NON RESPONDER (patient who has not obtained a reduction of at least 1 point in MAS of the degree of spastic hypertonia 4 weeks after administration), considering as possible any covariates the gender and age of the patient at the time of the acute event.

As regards the evaluation of secondary endpoints, the analysis of correlation (Pearson correlation index; Spearman correlation coefficient) was carried out in order to evaluate the association between the effects of the time elapsed from the acute event and the change in the score at MAS 4, 12 and 24 weeks after BoNT inoculation, as well as on the variation of the score at MI, FMA and MRS at 4, 12 and 24 weeks from the administration of BoNT-A.

The statistical analysis will be performed using the Statistical Package for Social Science SPSS® version 20.0 software for Macintosh (SPSS Inc., Chicago, IL, USA). Statistical significance will set at P <0.05.

Results are under statistical evaluation.

Tipo de estudio

De observación

Inscripción (Actual)

86

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Verona, Italia, 37124
        • Section of Clinical Neurology, Department Neurological, Neuropsychological, Morphological and Movement Sciences, University of Verona, Verona, Italy

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra de probabilidad

Población de estudio

Adult patients with the occurrence of post-stroke spastic hypertonia involving the main muscle groups of the affected side.

Descripción

Inclusion Criteria:

  • Diagnosis of spasticity as a consequence of cerebral stroke (ischemic or hemorrhagic) documented radiologically by brain CT or MRI;
  • Presence of spastic hypertonia in the main muscle groups of the affected side with an intensity equal to or greater than MAS 1+/4;
  • Presence of paresis in the affected side with weakness of the main muscle groups equal to or less than 2 according to the MRC scale;
  • Time elapsed since cerebral stroke less than 12 months;
  • No prior focal treatment of spasticity with botulinum toxin.

Exclusion Criteria:

  • Participation in other ongoing clinical studies
  • Presence of joint limitation or muscle contractures to the main muscle groups of the affected side quantifiable as a score of 4/4 at the MAS
  • Therapy with antispastic drugs (baclofen, dantrolene, tizanidine, benzodiazepines, clonidine, phenothiazine)
  • Other neurological (previous cerebral strokes, Parkinson's disease, multiple sclerosis, medullary pathologies, extrapyramidal syndromes) or orthopaedic (severe osteoarthritis, previous arthroplasty with residual joint limitation or fracture healed with angular defects) diseases involving the affected side and able to influence the results of the study.

Particularly vulnerable populations

The following cannot be included in the study:

  • women of childbearing age who do not use contraceptives
  • pregnant women
  • women in the breastfeeding period
  • patients in an emergency situation

Criteria for anticipated exit from the study:

  • Relapse of disease during the study period
  • Withdrawal of informed consent to participate in the study
  • Inability to perform the first follow-up evaluation 4 weeks after BoNT-A administration

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Enrolled patients

Each patient (whether hospitalized or outpatient) included in the study underwent to a baseline evaluation in which near and remote pathological history were recorded (main concomitant pathologies, drug therapy in progress, previous major surgery) and the following evaluation scales were administered: modified Ashworth scale (MAS), MI (motricity index), FMA (Fughl Meyer assessment) and Modified Rankin' scale (MRS).

Each patient will subsequently undergo to a follow-up evaluation at 4, 12 and 24 weeks after the date of inoculation through the execution of a specialist visit (physiatric/neurological) and the administration of the following evaluation scales: MAS, MI, FMA and MRS. For the duration of the study, each patient may undergo integrated rehabilitation treatment at the discretion of each of the investigators of each centre involved in the study according to the guidelines and common clinical practice.

There are no experimental interventions. The procedures are in line with normal clinical practice.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Time elapsed
Periodo de tiempo: T1 (4 weeks)

In order to evaluate the role of the time elapsed since the acute event on the therapeutic efficacy of the first administration of BoNT-A, the reduction of spastic hypertonia will be considered as the primary endpoint.

Patients who gain a reduction of at least 1 point at the modified Ashworth scale (MAS) were defined as "responder". Who did not achieve that amelioration was classified as "non-responders".

T1 (4 weeks)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Modified Ashworth scale (MAS)
Periodo de tiempo: T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)

Evaluation of the spasticity grade's at 4 - 12 - 24 weeks from the BoNT-A injection.

MAS is a scale graded in 5 points (0 no increase in muscle tone; 4 rigid in flexion or extension).

T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)
Motricity index (MI)
Periodo de tiempo: T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)

Evaluation of the motricity using the MI at 4 - 12 - 24 weeks from the BoNT-A injection.

Motricity Index is an ordinal scale that evaluates motor and functional capacity at the level of the limbs in patients with neurological pathologies. The movements evaluated are 6 in all (3 for each limb) and are:

  • for the arm (pinch grip, elbow flexion, shoulder abduction)
  • for the leg (ankle dorsiflexion, knee extension, hip flexion) To each movement assessed the points attributed may range from 0 "no movement" to 33 "normal pinch grip" or "normal power" for upper and lower extremities respectively.
T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)
Fughl Meyer assessment (FMA)
Periodo de tiempo: T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)
The Fugl-Meyer Assessment (FMA) is a stroke-specific, performance-based impairment index. It is designed to assess motor functioning, balance, sensation and joint functioning in patients with post-stroke hemiplegia. The scale is comprised of five domains (motor functioning in the upper and lower extremities; sensory functioning, evaluates light touch on two surfaces of the arm and leg, and position perception for 8 joints; balance, contains 7 tests, 3 seated and 4 standing; the joint range of motion, 8 joints; joint pain). Lowest is the total for each domain, worse is the correspondent function.
T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)
Modified rankin scale (MRS)
Periodo de tiempo: T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)
The Modified Rankin Scale (MRS) defines the physical and mental capacity to adapt to neurological deficits. The scale is divided into 6 degrees, from 0 (no deficit) to 5 (severe disability).
T0 (baseline); T1 (4 weeks); T2 (12 weeks); T3 (24 weeks)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Nicola Smania, MD, Universita di Verona

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

27 de julio de 2015

Finalización primaria (Actual)

31 de diciembre de 2018

Finalización del estudio (Actual)

31 de diciembre de 2018

Fechas de registro del estudio

Enviado por primera vez

15 de mayo de 2020

Primero enviado que cumplió con los criterios de control de calidad

21 de mayo de 2020

Publicado por primera vez (Actual)

28 de mayo de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

28 de mayo de 2020

Última actualización enviada que cumplió con los criterios de control de calidad

21 de mayo de 2020

Última verificación

1 de mayo de 2020

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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