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NCT Number: NCT06591091

Clemastine for Improving White Matter and Boosting Antidepressant Response in Late-life Depression

The goal of this study is to find out if the antihistamine, clemastine, can make the white matter in the brain better in older adults with depression. The study will also determine whether this improvement can make antidepressant treatment work better, reduce depressive symptoms, and improve memory and thinking.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Illinois College of Medicine

Chicago, Illinois, 60612, United States

Location status: Recruiting

Location contact

Olusola Ajilore, MD, PhD

CONTACT

[email protected]

312-413-4562

About this study

Geriatric depression, also known as late-life depression, is a type of major depression that affects people who are 60 years old or older. It can be difficult to treat and often comes back after treatment. It can also lead to problems with memory and thinking. Some studies have found that problems with the white matter in the brain can make it harder to treat depression in older adults. White matter helps with communication in the brain. A new study suggests that a medicine called clemastine might be able to improve the white matter in the brain. Clemastine is usually used as an antihistamine, but it might also help the brain repair itself. The goal of this study is to find out if clemastine can make the white matter in the brain better in older adults with depression. The study will also determine whether this improvement can make antidepressant treatment work better, reduce depressive symptoms, and improve memory and thinking. The study will involve two groups of participants. One group will receive the standard antidepressant treatment along with a placebo, while the other group will receive the standard antidepressant treatment along with clemastine. The investigators will compare the effects of these two treatments over a period of 12 weeks. The investigators will measure the improvement in white matter using special brain imaging techniques. The investigators will also assess the participants' mood, memory, and thinking abilities, and keep track of any side effects or problems caused by the treatments. Overall, this study has the potential to contribute valuable insights into the treatment of geriatric depression, alleviate depressive symptoms, enhance cognitive function, and potentially open up new avenues for future research and therapeutic approaches.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 60 years
  • Diagnosis of major depressive disorder, single or recurrent episode (DSM5)
  • Symptom Severity: MADRS ≥ 15
  • Seeking antidepressant treatment
  • Cognition score of MoCA >24
  • Fluent in English or Spanish

Exclusion criteria

  • Other Axis I psychiatric disorders, except for simple phobia or anxiety disorders present uniquely during the depressive episode (e.g., generalized anxiety disorder (GAD) or panic disorder symptoms)
  • History of alcohol or drug dependence or abuse in the last year
  • History of a developmental disorder or history of IQ (intelligence quotient) <70
  • Acute suicidality ideation within the past month as determined by the Columbia Suicide Severity Rating Scale (C-SSRS)
  • Acute grief (<1 month)
  • Current or past psychosis
  • Primary neurological disorder, including dementia, clinical stroke, brain tumor, epilepsy, etc.
  • Presence of unstable medical illness requiring urgent treatment
  • Any MRI contraindication
  • Electroconvulsive Therapy (ECT) in last 6 months

Treatment and study plan

Clemastine Fumarate

Drug

Listed in arm/group description

Other names: Clemastine, Tavist Allergy

Placebo

Drug

Listed in arm/group description

Primary outcomes

  1. Frequency, Intensity and Burden of Side Effects Rating Scale

    Time frame: 12 weeks

    The investigator will examine the safety of clemastine using the Frequency, Intensity, and Burden of Side Effects Rating Scale (FIBSER).

    The FIBSER is scored from 0-6, with higher scores indicating worse outcomes

  2. Montgomery-Asberg Rating Scale for Depression

    Time frame: 12 weeks

    The investigators will examine the effectiveness of an antidepressant plus clemastine (5.36 mg twice daily) compared to antidepressant plus placebo on clinical outcomes as indexed by the Montgomery-Asberg Rating Scale for Depression (MADRS).

    The MADRS is scored from 0-60, with higher scores indicating a worse outcome

  3. Quantitative Anisotropy

    Time frame: 12 weeks

    The investigators will measure the impact of an antidepressant plus clemastine (5.36 mg twice daily) compared to antidepressant plus placebo on white matter integrity as indexed by change in quantitative anisotropy (QA).

    QA has no units but is measured from 0 to 1 and a higher indicates better white matter integrity

  4. Fractional Anisotropy

    Time frame: 12 weeks

    The investigators will measure the impact of an antidepressant plus clemastine (5.36 mg twice daily) compared to antidepressant plus placebo on white matter integrity as indexed by change in fractional anisotropy (FA).

    FA has no units but is measured from 0 to 1 and a higher indicates better white matter integrity

Secondary outcomes

  1. Trail Making Test Part A and Part B

    Time frame: 12 weeks

    The investigators will examine the effectiveness of an antidepressant plus clemastine (5.36 mg twice daily) compared to antidepressant plus placebo on cognitive outcomes as indexed by Trail Making Test Parts A and B.

    The Trail Making Test A and B is scored by the time to completion (seconds) and number of errors, with higher scores indicating worse performance.

    For TMT Part A and Part B, the "average" and "deficient" scores are categorized as follows:

    TMT Part A 29 seconds (average) Over 79 seconds (Deficient) TMT Part B 75 seconds (average) Over 273 seconds (Deficient)

  2. Orientation Dispersion Index

    Time frame: 12 weeks

    The investigators will measure the impact of an antidepressant plus clemastine (5.36 mg twice daily) compared to antidepressant plus placebo on white matter integrity as indexed by change in neurite orientation dispersion and density imaging (NODDI)-derived orientation dispersion index (ODI).

    The ODI has no units but ranges from 0-1, with higher values indicating more neurite dispersion.

  3. Neurite Density Index

    Time frame: 12 weeks

    The investigators will measure the impact of an antidepressant plus clemastine (5.36 mg twice daily) compared to antidepressant plus placebo on white matter integrity as indexed by change in neurite orientation dispersion and density imaging (NODDI)-derived measured neurite density index (NDI).

    The NDI has no units but ranges from 0-1, with higher values indicating more intracellular diffusion

Study contacts

Contact information is provided by the study sponsor or research team.

Olu A Ajilore, MD, PhD

CONTACT

[email protected]

312-413-4562

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Collaborators

  • Cures Within Reach

Registry information

Acronym: CLIMB

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 19, 2024
Registry last updated
Jun 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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