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

20 października 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Aktywny, nie rekrutujący

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Szacowany)

8

Faza

  • Faza 2
  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Toledo
      • Toledo, Toledo, Hiszpania
        • Hospital Nacional de Parapléjicos

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 75 lat (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

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 studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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).

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP).
Ramy czasowe: 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).

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Six-Minute Walk Test (6MWT).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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.
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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)

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Columbia-Suicide Severity Rating Scale (C-SSRS).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).
Ramy czasowe: 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).

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

13 maja 2026

Zakończenie podstawowe (Szacowany)

1 sierpnia 2027

Ukończenie studiów (Szacowany)

1 sierpnia 2027

Daty rejestracji na studia

Pierwszy przesłany

20 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

22 września 2026

Pierwszy wysłany (Rzeczywisty)

25 września 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

21 października 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

20 października 2026

Ostatnia weryfikacja

1 października 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • Rimohandopen
  • 2025 (Grant/umowa NIH USA)
  • 2025-524279-22-00 (Ctis)

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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