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Rimonabant for Cognitive Impairment in People With Post-COVID-19 Syndrome (RIMOCOVID-1)

10. november 2026 oppdatert av: Sinfatin S.L

Effects of a CB1 Receptor Antagonist/Inverse Agonist (Rimonabant) on the Improvement of Cognitive Impairment in Patients With Post-COVID-19 Syndrome (RIMOCOVID-1)

The main goal of the study is to assess the effect of rimonabant in cognitive performance in patients with Post-COVID-19 Syndrome, also known as long COVID.

The study will include 80 adults aged 18 to 75 years that will receive either rimonabant (5 mg) or placebo (a look-alike tablet that contains no drug) once daily for 90 days. Neither the participants nor the investigators will know which treatment is being given.

The study will also help to learn about the safety of rimonabant.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

RIMOCOVID-1 is a phase IIb proof-of-concept study investigating rimonabant for cognitive impairment associated with post-COVID-19 syndrome. The scientific rationale is based on the hypothesis that altered neuronal excitability contributes to central fatigue and cognitive dysfunction in this population.

Rimonabant is a selective cannabinoid type 1 (CB1) receptor antagonist/inverse agonist. CB1 receptors are involved in neurotransmission and the regulation of neuronal excitability. Neurophysiological research and previous preclinical and clinical studies in other populations provide the rationale for investigating whether CB1 receptor modulation can improve cognitive performance and associated functional limitations in people with post-COVID-19 syndrome.

The selected dose and treatment duration are informed by previous experience with low-dose rimonabant in neurological conditions. The study will evaluate whether this approach produces measurable clinical benefits while characterizing its safety and tolerability in the study population.

Given the psychiatric adverse effects previously associated with rimonabant, the protocol includes targeted screening and ongoing monitoring for depression, anxiety, suicidal ideation, and other changes in mental health. Safety surveillance includes validated questionnaires, clinical assessments, and participant diaries with weekly mood ratings. Predefined criteria guide treatment discontinuation and specialist assessment when indicated.

Participants may continue usual care and rehabilitation in accordance with the protocol's restrictions on concomitant treatments. Assessments after the scheduled end of treatment will evaluate safety and whether any observed clinical changes persist.

Studietype

Intervensjonell

Registrering (Antatt)

80

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

      • Albacete, Spania, 02006
        • Hospital Universitario de Albacete
        • Ta kontakt med:
      • Madrid, Spania, 28040
        • Hospital Clinica San Carlos HCSC
        • Ta kontakt med:
      • Toledo, Spania, 45004
        • Hospital Nacional de Paraplejicos
        • Ta kontakt med:
    • Donostia

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Age between 18 and 75 years (both inclusive).
  • Have had COVID-19 at least 3 months before joining the study.
  • Have been diagnosed with active PCS (Long COVID).
  • Have ongoing problems with memory or concentration due to long-COVID syndrome.
  • Show signs of cognitive impairment in study assessments.
  • Be willing to complete study assessments.
  • Be able to understand and speak Spanish.
  • Provide written consent to participate.

Exclusion Criteria:

  • Have an active or recent COVID-19 infection.
  • Have a high risk of suicide.
  • Have severe mental health conditions, a pprevious suicide attempt.
  • Have neurological conditions that may affect memory or concentration.
  • Have other medical conditions that could explain their symptoms.
  • Have severe lung, heart, liver, kidney, or bone disease
  • Have a body mass index (BMI) greater than 40 kg/m²
  • Are unable to walk or attend study visits.
  • Use substances or medications that may affect memory or concentration.
  • Are taking medicines that may interact with the study treatment.
  • Have a known allergy to rimonabant.
  • Have taken part in another clinical trial within the last month.
  • Are pregnant or breastfeeding.
  • Are able to become pregnant or father a child and are not using effective contraception.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Rimonabant 5 mg

Participants receive rimonabant 5 mg orally once daily for 90 days.

Rimonabant 2.5 mg tablets. Two tablets are taken together orally once a day in fasted conditions, providing a total daily dose of 5 mg. Treatment duration is 90 days.

Placebo komparator: Placebo

Participants receive matching placebo orally once daily for 90 days.

Placebo tablets matching the appearance of the rimonabant tablets. Two tablets are taken together orally once daily in fasted conditions. Treatment duration is 90 days.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Symbol Digit Modalities Test (SDMT)
Tidsramme: Baseline to end of follow-up (day 135)

The SDMT assesses cognitive processing speed using the validated Spanish version of the test. Participants must match symbols to their corresponding numbers within 90 seconds. The raw score is the number of correct responses, ranging from 0 to 110; higher scores indicate better performance. Age- and education-adjusted scores are calculated using Spanish normative data.

Baseline to end of follow-up (day 135)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Borg CR10 Scale
Tidsramme: Baseline to end of follow-up (day 135)

The Borg CR10 Scale assesses perceived exertion after the 6MWT. Scores range from 0 (no exertion) to 10 (maximal exertion). Higher scores indicate greater perceived exertion.

Baseline to end of follow-up (day 135)
Fatigue Severity Scale (FSS)
Tidsramme: Baseline to end of follow-up (day 135)

The Fatigue Severity Scale assesses fatigue severity and its impact on daily functioning during the preceding week. It consists of nine items rated from 1 to 7. The mean score ranges from 1 to 7. Higher scores indicate greater fatigue severity.

Baseline to end of follow-up (day 135)
Complutense Verbal Learning Test (TAVEC)
Tidsramme: Baseline to end of follow-up (day 135)

The TAVEC assesses verbal learning and episodic memory through repeated word-list learning, interference, delayed recall, and recognition tasks. Age-adjusted standardized scores characterize verbal learning and memory performance.

Baseline to end of follow-up (day 135)
Frontal Assessment Battery (FAB)
Tidsramme: Baseline to end of follow-up (day 135)

The Frontal Assessment Battery assesses executive function through six subtests. The total score ranges from 0 to 18. Higher scores indicate better executive functioning.

Baseline to end of follow-up (day 135)
Medical Outcomes Study Sleep Scale (MOS-SS)
Tidsramme: Baseline to end of follow-up (day 135)

The MOS Sleep Scale assesses sleep quality and sleep-related problems during the preceding four weeks. Scaled domain scores range from 0 to 100. Higher sleep-problem scores indicate worse sleep, whereas higher sleep-adequacy scores indicate better sleep adequacy.

Baseline to end of follow-up (day 135)
Brain Fog Scale
Tidsramme: Baseline to end of follow-up (day 135)

The Brain Fog Scale assesses subjective cognitive symptoms, including mental clouding, slowed thinking, and difficulties with concentration and attention. Higher total scores indicate greater perceived cognitive impairment.

Baseline to end of follow-up (day 135)
Sustained Attention to Response Task (SART)
Tidsramme: Baseline to end of follow-up (day 135)

The SART assesses sustained attention and inhibitory control through a computerized go/no-go task. Participants respond to frequent non-target digits and withhold responses to the infrequent target digit 3. Recorded variables include reaction time, commission errors (responses to the target), and omission errors (missed responses to non-targets). Reaction time reflects response speed, while higher error counts indicate poorer sustained attention or inhibitory control.

Baseline to end of follow-up (day 135)
Stroop Test
Tidsramme: Baseline to end of follow-up (day 135)

The Stroop Test assesses cognitive inhibition and processing speed through congruent and incongruent conditions. Recorded variables include reaction time and the number of errors in each condition. Longer reaction times indicate slower performance, while higher error counts indicate poorer accuracy.

Baseline to end of follow-up (day 135)
Beck Depression Inventory-II (BDI-II)
Tidsramme: Baseline to end of follow-up (day 135)

The Beck Depression Inventory-II assesses depressive symptom severity over the preceding two weeks. It consists of 21 items scored from 0 to 3. The total score ranges from 0 to 63. Higher scores indicate more severe depressive symptoms.

Baseline to end of follow-up (day 135)
Hospital Anxiety and Depression Scale (HADS)
Tidsramme: Baseline to end of follow-up (day 135)

The Hospital Anxiety and Depression Scale assesses symptoms of anxiety and depression over the preceding week. It consists of 14 items scored from 0 to 3. The combined total score ranges from 0 to 42. Higher scores indicate greater symptom severity.

Baseline to end of follow-up (day 135)
Six-Minute Walk Test (6MWT)
Tidsramme: Baseline to end of follow-up (day 135)

The Ten-Meter Walk Test assesses walking performance by measuring the time required to walk 10 meters, expressed in seconds. Shorter completion times indicate faster walking performance.

Baseline to end of follow-up (day 135)
Timed Up and Go (TUG) Test
Tidsramme: Baseline to end of follow-up (day 135)

The Timed Up and Go Test assesses functional mobility by measuring the time required to rise from a chair, walk three meters, turn, return to the chair, and sit down. Completion time is expressed in seconds. Shorter times indicate better functional mobility.

Baseline to end of follow-up (day 135)
Patient Global Impression of Change (PGIC)
Tidsramme: End of treatment (day 90) and End of follow-up (day 135)

The Patient Global Impression of Change assesses the participant's overall perception of improvement or worsening compared with their condition at baseline. Participants report whether their overall condition has improved, remained unchanged, or worsened.

End of treatment (day 90) and End of follow-up (day 135)
EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)
Tidsramme: Baseline and End of follow-up (day 135)

The EQ-5D-5L assesses health-related quality of life across five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five response levels, from no problems to extreme problems or inability to perform the activity. Higher dimension levels indicate greater health problems.

Baseline and End of follow-up (day 135)
Overall Mood Scale
Tidsramme: Baseline to end of follow-up (day 135)

The Overall Mood Scale assesses the participant's overall mood using a numerical rating from 0 (very poor mood) to 10 (excellent mood). Participants complete the rating at baseline and weekly in their diary. Higher scores indicate better mood.

Baseline to end of follow-up (day 135)
Treatment-Emergent Adverse Events AEs
Tidsramme: First dose of study medication to end of follow-up (day 135)

Safety is assessed by the number of participants experiencing at least one adverse event beginning after the first administration of study medication. Events are classified by severity and relationship to study medication. Serious adverse events, adverse events of special interest, and events leading to withdrawal are summarized separately.

First dose of study medication to end of follow-up (day 135)
Visual Analogue Scale (VAS)
Tidsramme: Baseline to end of follow-up (day 135)

The VAS assesses self-perceived health using a 10-cm horizontal line. The left end represents very poor health, and the right end represents very good health. Participants mark the point that best reflects their perceived health status. Positions closer to the right end indicate better perceived health.

Baseline to end of follow-up (day 135)
Cognitive Fatigue Rate
Tidsramme: Baseline to end of follow-up (day 135)

Cognitive fatigue is assessed using the Cognitive Fatigue Index derived from the SDMT (CFI-SDMT), which reflects the relative change in correct responses between the initial and final 30-second intervals of the 90-second test. Negative values indicate declining performance. Measures include the CFI-SDMT score and the percentage of participants presenting cognitive fatigue, defined as a decline in performance of more than 10% between these intervals.

Baseline to end of follow-up (day 135)
Responder Rates
Tidsramme: Baseline to end of follow-up (day 135)

Responder rates are reported separately as the percentage of participants achieving an increase of at least 4 points in the SDMT total raw score from baseline and the percentage achieving an improvement of at least 10% in the CFI-SDMT from baseline.

Baseline to end of follow-up (day 135)

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Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

6. november 2026

Primær fullføring (Antatt)

1. mars 2028

Studiet fullført (Antatt)

1. mars 2028

Datoer for studieregistrering

Først innsendt

3. november 2026

Først innsendt som oppfylte QC-kriteriene

10. november 2026

Først lagt ut (Faktiske)

12. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

12. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

10. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • RIMOCOVID-1
  • 2023 (U.S. NIH-stipend/kontrakt)
  • 2023-507870-42 (EudraCT-nummer)

Plan for individuelle deltakerdata (IPD)

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Studerer et amerikansk FDA-regulert medikamentprodukt

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Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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