Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

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

20. Oktober 2026 aktualisiert von: 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.

Studienübersicht

Status

Aktiv, nicht rekrutierend

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

8

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Toledo
      • Toledo, Toledo, Spanien
        • Hospital Nacional de Parapléjicos

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 75 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
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).

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP).
Zeitfenster: 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).

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Six-Minute Walk Test (6MWT).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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.
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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)

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Columbia-Suicide Severity Rating Scale (C-SSRS).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).
Zeitfenster: 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).

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

13. Mai 2026

Primärer Abschluss (Geschätzt)

1. August 2027

Studienabschluss (Geschätzt)

1. August 2027

Studienanmeldedaten

Zuerst eingereicht

20. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

22. September 2026

Zuerst gepostet (Tatsächlich)

25. September 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

21. Oktober 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

20. Oktober 2026

Zuletzt verifiziert

1. Oktober 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • Rimohandopen
  • 2025 (US NIH Stipendium/Vertrag)
  • 2025-524279-22-00 (Ctis)

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .