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Effect of Rimonabant on Hand Function in Patients With Spinal Cord Injury (RIMOHANDOPEN)

20 de octubre de 2026 actualizado por: Sinfatin S.L

Exploratory Study on the Effect of Rimonabant on Hand Function in Patients With Spinal Cord Injury (RIMOHANDOPEN)

This is an one arm study to be conducted in spinal cord injury patients. The goal of this clinical trial is to learn if rimonabant improves hand motor and performance function in patients with cervical spinal cord injury. It will also learn about the safety of rimonabant.

Participants will: Take 5 mg of rimonabant every day for 90 days. Visit the clinic once every 15-30 days for checkups and tests.

Descripción general del estudio

Estado

Activo, no reclutando

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

8

Fase

  • Fase 2
  • Fase 1

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

    • Toledo
      • Toledo, Toledo, España
        • Hospital Nacional de Parapléjicos

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 a 75 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Age between 18 and 75 years.
  2. At least 2 months since spinal cord injury.
  3. Cervical spinal cord injury (C1-C8) with AIS A-D.
  4. Muscle strength should be within a range of 5 to 40 points on the UEMS score.
  5. Capacity to provide informed consent.

Exclusion Criteria:

  1. High suicide risk assessed by C-SSRS.

  2. History of severe psychiatric disorders, major depression or prior suicide attempts.

  3. Treatment with anticoagulants or strong CYP3A4 inhibitors or inducers (inhibitors such as ketoconazole, itraconazole, ritonavir, telithromycin, clarithromycin, or nefazodone, and inducers such as rifampicin, phenytoin, phenobarbital, carbamazepine, or St. John's Wort).

  4. Body Mass Index (BMI) > 40 kg/m².

  5. Pregnancy or breastfeeding.

  6. Fertile men or women who cannot guarantee the use of highly effective contraceptive methods, as defined by the European HMA-CTFG guidelines-i.e., those with a failure rate of less than 1 % per year when used consistently and correctly (1).

    A woman is considered fertile if she is physiologically capable of becoming pregnant, from menarche until postmenopausal, unless permanently sterile. Permanent sterilization methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy. A woman is considered postmenopausal after spontaneous amenorrhea for at least 12 consecutive months with no alternative medical cause. An elevated follicle-stimulating hormone (FSH) level in the postmenopausal range may be used to support the diagnosis in women not using hormonal contraception or hormone replacement therapy. However, in the absence of 12 months of amenorrhea, a single FSH measurement is not sufficient.

    Acceptable highly effective contraceptive methods include:

    • Combined hormonal contraception (containing estrogen and progestogen) associated with ovulation inhibition, administered orally, vaginally, or transdermal.
    • Progestogen-only hormonal contraception associated with ovulation inhibition (oral, injectable, or implantable).
    • Intrauterine device (IUD).
    • Intrauterine hormone-releasing system (IUS).
    • Bilateral tubal occlusion.
    • Vasectomized partner: provided this is the participant's sole sexual partner and the vasectomy has been medically confirmed as successful.
    • Sexual abstinence: refraining from heterosexual intercourse during the entire treatment and follow-up period.
  7. Uncontrolled hypothyroidism, or a history of severe bone, liver, or kidney disease.

  8. Inability to attend hospital visits.

  9. Known allergy to rimonabant or any of the excipients used.

  10. Participation in another clinical trial with pharmacological intervention within the month prior to enrolment.

  11. Any other condition that, in the opinion of the investigator, makes the subject's participation in the study unrecommended, such as severe heart failure or uncontrolled diabetes.

  12. Contraindications for transcranial magnetic stimulation (TMS), such as metal implants in the head, pacemakers, epileptic seizures in the last two years, or other implanted electronic devices.

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

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment

This arm will receive two tablets of rimonabant 2.5 mg (total of 5 mg), once daily for 90 days

Two tablets of rimonabant 2.5 mg (5 mg per day).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

The Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) evaluates upper-limb sensorimotor and prehension function. Five subtests are assessed for each upper limb: dorsal sensation (0-12), palmar sensation (0-12), strength (0-50), prehension ability (0-12), and prehension performance (0-30). The maximum score is 116 points per upper limb. Higher scores indicate better upper-limb sensorimotor and prehension function.

From start of study treatment (day 0) until end of follow-up (day 120).

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Six-Minute Walk Test (6MWT).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The Six-Minute Walk Test (6MWT) assesses functional walking capacity and endurance by measuring the total distance the participant is able to walk during six minutes. Greater distance walked indicates better walking endurance and functional capacity

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Ten-Meter Walk Test (10MWT).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The Ten-Meter Walk Test (10MWT) assesses walking performance by measuring the time required to walk 10 meters at a comfortable or maximal pace. Shorter completion times indicate faster walking performance.

Walking speed over 10 meters is reported in meters/second.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Berg Balance Scale (BBS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The Berg Balance Scale comprises 14 tasks scored from 0 to 4.

Total scores range from 0 to 56; higher scores indicate better balance.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Walking Index for Spinal Cord Injury II (WISCI-II).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Assesses walking ability according to physical assistance, braces and assistive devices.

Scores range from 0 to 20; higher scores indicate greater walking independence.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Finger Tapping Test (FTT).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Motor speed and coordination are assessed as the number of finger taps completed during the predefined test interval.

Higher values indicate better motor speed/performance.

From start of study treatment (day 0) until end of follow-up (day 120).
Box and Block Test (BBT).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Gross manual dexterity is assessed as the number of blocks transferred between compartments in 60 seconds.

Higher values indicate better manual dexterity.

From start of study treatment (day 0) until end of follow-up (day 120).
Nine-Hole Peg Test (9HPT).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Fine manual dexterity is assessed as the time, in seconds, required to place and remove nine pegs.

Lower completion times indicate better manual dexterity.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Dynamometry.
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Maximum handgrip force is measured using a handheld dynamometer.

Higher values indicate greater handgrip strength.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Upper Extremity Motor Score (UEMS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

UEMS evaluates five key upper-limb muscle groups bilaterally, each scored from 0 to 5.

Total score ranges from 0 to 50; higher scores indicate greater upper-limb motor strength.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Functional Reach Test (FRT).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Measures the maximum forward reaching distance without loss of stability.

Higher values indicate greater functional reach and dynamic balance.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Borg Category-Ratio 10 (Borg CR10).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Perceived exertion is assessed using the Borg CR10 Scale.

Scores range from 0 to 10, with higher scores indicating greater perceived exertion/fatigue.

From start of study treatment (day 0) until end of follow-up (day 120).
Visual Analogue Scale for Fatigue (VAS-F).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Used to assess the participant's subjective perception of fatigue intensity. Participants rate their perceived fatigue following the Finger Tapping Test (FTT).

Scores range from 0 to 10, with higher scores indicating greater perceived fatigue.

Changes from baseline will be evaluated during treatment and follow-up.

From start of study treatment (day 0) until end of follow-up (day 120).
Fatigue Severity Scale (FSS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

To evaluates fatigue severity. Scores ≥ 4 indicate clinically significant fatigue.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Multidimensional Fatigue Inventory (MFI-20).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Measures five dimensions of fatigue, offering a comprehensive assessment of fatigue impact.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Breathing test.
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

To assess the participant's respiratory function and lung capacity.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Oximetry.
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Non-invasively measures blood oxygen saturation and heart rate

From start of study treatment (day 0) until end of follow-up (day 120).
International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120)

The ISNCSCI are systematically assesses motor and sensory function to detemine the neurological level and completenees of spinal cord injury.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120)
Motor Evoked Potentials (MEPs).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Transcranial magnetic stimulation (TMS) is used to assess corticospinal excitability and motor pathway integrity by recording motor evoked potentials (MEPs). Changes in MEPs from baseline will be assessed throughout treatment and follow-up.

From start of study treatment (day 0) until end of follow-up (day 120).
Somatosensory Evoked Potentials (SEPs).
Periodo de tiempo: From start of study treatment (day 0) until end of follow-up (day 120).

Somatosensory evoked potentials (SEPs) are recorded following peripheral nerve electrical stimulation to assess sensory pathway conduction and integrity through cortical responses.

From start of study treatment (day 0) until end of follow-up (day 120).
Spinal Cord Independence Measure III (SCIM-III).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The Spinal Cord Independence Measure III (SCIM-III) assesses functional independence in activities of daily living, mobility, and sphincter management and provides an overall measure of functional recovery. Higher scores indicate greater functional independence.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Medical Outcomes Study Sleep Scale (MOS-SS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The Medical Outcomes Study Sleep Scale (MOS-SS) assesses multiple aspects of sleep during the previous four weeks, including sleep quality, sleep disturbances, somnolence, and sleep adequacy.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Patient Global Impression of Change score (PGIC).
Periodo de tiempo: Visit 03 (day 30), visit 06 (day 90) and follow-up (day 120)

The Patient Global Impression of Change (PGIC) assesses the participant's subjective perception of overall improvement or deterioration since the beginning of the study.

Visit 03 (day 30), visit 06 (day 90) and follow-up (day 120)

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Columbia-Suicide Severity Rating Scale (C-SSRS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60) and visit 06 (day 90).

Is used to monitor suicidal ideation and behavior. A suicidality alert is defined in the protocol as a positive C-SSRS response indicating suicidal ideation with intent, preparatory behavior, or suicide attempt. The outcome will report the number of participants meeting the protocol-defined suicidality criteria

Baseline, visit 03 (day 30), visit 05 (day 60) and visit 06 (day 90).
Adverse Events (AEs).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Is an adverse event with onset after the first administration of rimonabant. The outcome will report the number of participants experiencing at least one TEAE. Events will be assessed for intensity, seriousness, and relationship to the investigational medicinal product and coded by System Organ Class and Preferred Term.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Serious Adverse Events (SAEs).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The outcome will report the number of participants experiencing at least one serious adverse event meeting the protocol-defined seriousness criteria, including death, life-threatening events, hospitalization or prolongation of hospitalization, significant disability or incapacity, congenital anomaly/birth defect, or other clinically important medical events.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Adverse Events of Special Interest (AESIs).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The outcome will report the number of participants experiencing at least one protocol-defined adverse event of special interest. Particular attention is given to psychiatric events and clinically relevant changes in mental status because of the known psychiatric risk profile of rimonabant.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
The Visual Analogue Scale for Pain (VAS-P).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Assesses the participant's subjective perception of pain intensity. Changes from baseline will be used to identify clinically significant changes in pain during treatment and follow-up.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Modified Ashworth Scale (MAS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Is used to assess changes in muscle spasticity during the study. Higher grades indicate greater muscle tone/spasticity

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
The Penn Spasm Frequency Scale (PSFS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Is used to assess changes in the frequency of muscle spasms during the study. Higher scores indicate a greater frequency of muscle spasms.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Beck Depression Inventory-II (BDI-II).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Is used to monitor depressive symptoms during the study. Higher scores indicate greater severity of depressive symptoms. According to the protocol, a score ≥20 triggers a moderate psychiatric alert and a score ≥29 triggers a high psychiatric alert requiring confirmation and specialist assessment.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).
Hospital Anxiety and Depression Scale (HADS).
Periodo de tiempo: Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

The Hospital Anxiety and Depression Scale (HADS) assesses anxiety or depression symptoms. Higher scores indicate greater symptom severity. According to the protocol, a subscale score (either anxiety or depression) ≥11 triggers a moderate alert and ≥15 a high psychiatric alert.

Baseline, visit 03 (day 30), visit 05 (day 60), visit 06 (day 90) and follow-up (day 120).

Colaboradores e Investigadores

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

Patrocinador

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)

13 de mayo de 2026

Finalización primaria (Estimado)

1 de agosto de 2027

Finalización del estudio (Estimado)

1 de agosto de 2027

Fechas de registro del estudio

Enviado por primera vez

20 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

22 de septiembre de 2026

Publicado por primera vez (Actual)

25 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

21 de octubre de 2026

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

20 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • Rimohandopen
  • 2025 (Subvención/contrato del NIH de EE. UU.)
  • 2025-524279-22-00 (Ctis)

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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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