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DepressionPhase 4NCT04400266

Buspirone and Melatonin for Depression Following Traumatic Brain Injury

A Phase 4 study testing Buspirone and Mealatonin in people with Depression and Brain Injuries, Traumatic, run by Massachusetts General Hospital at 2 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Traumatic brain injuries (TBIs) are common. Post-TBI depression is associated with anxiety, aggression, fatigue, distractibility, anger, irritability, and rumination. The current research group conducted a pilot clinical trial, which investigated the novel treatment combination of buspirone and melatonin (B+MEL) in… Read more about this study

Who is it for?
Ages 18 to 64 years
Conditions the study is for
Depression, Brain Injuries, Traumatic
What is being tested?
Buspirone and Mealatonin
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
2 sitesUnited States
Study dates
1 Aug 2020to 31 Jul 2028
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 64 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Patients with mild or moderate TBI will be included. To be included, a subject must meet the criteria below:
  • Non-penetrating mild or moderate traumatic brain injury that occurred 3 or more months prior to study entry (to minimize natural recovery from TBI)
  • Age: 18-64 years
  • Meeting any one of the following severity criteria, as documented in the patient's medical records:
  • Glasgow Coma Scale (GCS) score of 9-15 within 4 hours after injury
  • Loss of consciousness (LOC) >1 minute and <=24 hours
Show all 11Show fewer
  • Post-traumatic amnesia (PTA) < 7 days
  • English-speaking
  • Current DSM-5 diagnosis of Major Depressive Episode by medical record diagnosis
  • HAM-D-21 score of 18 or higher
  • Patients who are considered to be appropriate by their clinician and who are willing to be started on Buspirone and Melatonin for clinical purposes.

Who cannot join

  • History of neurological disorder (e.g., stroke, epilepsy, multiple sclerosis, HIV, neurodegenerative disorders) or any acute or unstable medical condition that is likely to interfere with the assessments or with participation in treatment, as determined by history by the patient or review of their medical records.
  • Evidence from the history of TBI severity greater than moderate, i.e., GCS of 8 or less, LOC > 24 hours, or PTA > 7 days.
  • Inability to attend regular appointments
  • Imminent risk of suicide, as determined by the assessing clinician; HAM-D, Question 3, answers > 1; SDQ, Question 11, answers > 3; spontaneous expressions of suicidal ideation will result in emergency evaluation by a licensed clinician member of study staff for appropriate assessment and triage.
  • Lifetime history of schizophrenia or other primary psychotic disorders, as determined by history by the patient or review of their medical records.
  • History of bipolar disorder, as determined by history by the patient or review of their medical records.
Show all 12Show fewer
  • Alcohol or substance dependence in the past 3 months, as determined by history by the patient or review of their medical records.
  • Pregnancy or breast-feeding
  • Concomitant use of buspirone, any psychostimulant, or modafinil/armodafinil
  • Patients currently on an antidepressant or who have been on antidepressant in the past 4 weeks
  • Patients with prior intolerances to buspirone or melatonin.
  • Conditions that would preclude a subject from participating in the MRI procedures (e.g., metal implants, aneurysm clips, shrapnel/retained particles, pacemakers, claustrophobia).

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Kaloyan Tanev contact

6177267511

ktanev@partners.org

United States2 sites, 2 recruiting
  • Massachusetts General Hospital

    Boston, Massachusetts, 02144

    Kaloyan S Tanev, MD, 617-726-7511, ktanev@partners.org

    Mu-Yin Chang, (617) 283-2530, mchang11@mgh.harvard.edu

    Recruiting
  • Massachusetts General Hospital Home Base Program

    Charlestown, Massachusetts, 02129

    Kaloyan Tanev, MD, 617-764-6476, ktanev@bwh.harvard.edu

    Mu-Yin Chang, BA, (617) 283-2530, mchang11@mgh.harvard.edu

    Recruiting

Other trials in United States

About this study

Traumatic brain injuries (TBIs) are common. Post-TBI depression is associated with anxiety, aggression, fatigue, distractibility, anger, irritability, and rumination. The current research group conducted a pilot clinical trial, which investigated the novel treatment combination of buspirone and melatonin (B+MEL) in outpatients with clinical depression. Compared to placebo, B+MEL was associated with a significant improvement in depressive symptoms. Depression following TBI may be different from clinical depression. The B+MEL combination has never been studied in patients with post-TBI depression. The B+MEL has shown promise in ameliorating cognitive difficulties in people with depression. Because cognitive problems are typical in people with post-TBI depression, we plan to measure the effect of the B+MEL combination on cognitive ability in post-TBI depression. Additionally, we are interested in measuring functional magnetic resonance imaging changes before and after treatment with B+MEL in order to gain insight into the brain mechanisms of our hypothesized clinical symptom changes.

The goals of the proposed pilot research project are to assess changes in symptoms in patients with post-TBI depression following Buspirone + Melatonin combination (B+MEL), and the corresponding brain mechanisms underlying these hypothesized changes by measuring: 1) depressive symptoms; 2) cognitive symptoms; 3) functional magnetic resonance imaging.

Read the detailed description

Background and significance:

Buspirone and Melatonin Combination for the Treatment of Post-TBI Depression Traumatic brain injuries (TBIs) are common (1.7 million cases each year in the US), and major depressive disorder (MDD) occurs in up to 33% of TBI patients. Post- TBI depression is associated with anxiety, aggression, fatigue, distractibility, anger, irritability, and rumination. The current research group conducted a pilot clinical trial, which investigated the novel treatment combination of buspirone (15 mg/day) and melatonin (3mg), in a small outpatient cohort with MDD. Compared to the placebo group, the B+MEL group demonstrated significant improvements in depressive symptoms, at buspirone doses significantly below the recommended therapeutic range for anxiety and recommended dose (40-60 mg) for MDD. Compared to placebo, B+MEL was associated with a significant antidepressant response on the Clinical Global Impressions- Severity (CGI-S, p=0.046) and -Improvement (CGI-I, p=0.04) scales, and on the Inventory of Depressive Symptomatology (IDS, p=0.034). B+MEL was also superior to the pooled buspirone and placebo populations (CGI-S, p=0.009; CGI-I, p=0.021; IDS, p=0.031). This treatment combination has never been studied in patients with post-TBI depression. Depression following TBI may be phenomenologically and neurobiologically distinct from MDD, and the neuroanatomical and biopsychological mechanisms underlying B+MEL response in post-TBI depression are currently unknown. The goal of the proposed pilot research project is to generate pilot data that would serve as a base for an R01 application for a study that will fill this critical gap.

Buspirone and Melatonin Combination and Its Effect on Cognition The current research group compared the effects of B+MEL, buspirone, and placebo on the self-rated Cognitive and Physical Functioning Questionnaire (CPFQ). The CPFQ cognitive dimension score favored the B+MEL combination treatment, compared to the pooled buspirone and placebo groups (p = 0.050). In another randomized, double-blind, SPCD clinical study by the current research group, treatment with NSI-189 - a compound shown to stimulate neurogenesis in in vitro and in vivo, was associated with improvement in cognition, objectively measured by the dimensions of memory (p=0.002) and attention (p=0.048), compared to placebo in MDD patients. The etiology of cognitive impairment in post-TBI depression is complex, and the cognitive changes in response to this novel treatment combination has not been investigated. A possible mechanism of B+MEL action could be the promotion of neurogenesis. Although studying neurogenesis is beyond the scope of the current research, we speculate that a treatment stimulating neurogenesis may contribute to cognitive improvements in post-TBI depression. Hence, we will investigate the effect of B+MEL on cognitive measures of verbal memory, executive functioning, and speed of information processing, in post-TBI depression pre and post-treatment.

Resting State Functional Connectivity in Depression and in TBI MDD is characterized by altered resting state functional connectivity (rsFC) between distinct neural networks. A recent study compared rsFC in TBI with co-morbid depressive symptoms, relative to TBI without depressive symptoms. The results demonstrated increased rsFC between the amygdala and parts of the DAN, salience, somatomotor, and visual networks. Meta-analyses investigating fMRI-based rsFC in MDD demonstrated decreased rsFC within the frontoparietal control network (FPCN), and increased rsFC within the default network (DN). Increased rsFC between the FPCN and DN, and decreased rsFC between the FPCN and dorsal attentional network (DAN) may reflect increased attentional bias toward ruminative thoughts. Decreased rsFC between the affective network (AN) and medial prefrontal cortex may reflect impaired emotional regulation and arousal. Altered rsFC between the ventral attentional network (VAN) and posterior regions may reflect impaired salience detection in MDD. Changes in rsFC have been detected in response to different treatments, such as medication and cognitive behavioral therapy, for depression. Altered rsFC in post-TBI depression is associated with cognitive impairments. A neuroimaging study measuring rsFC in post-TBI depression has not been performed in the context of the novel B+MEL combination treatment. The proposed research is novel with respect to design, technology, and its multi-level integration probing psychological and neurobiological constructs assumed to be critically implicated depression following TBI. Furthermore, it may provide valuable insight regarding rsFC biomarkers implicated in the effective treatment of post-TBI depression.

Specific Aims Specific Aim 1: Assess the changes in depressive symptoms following Buspirone + Melatonin combination (B+MEL) in post-TBI depression.

Hypothesis 1: The B+MEL treatment combination will be associated with improvements in depressive symptoms (changes in HAM-D scores pre- to post-treatment).

Specific Aim 2: Assess the changes in cognitive symptoms following Buspirone + Melatonin combination (B+MEL) in post-TBI depression.

Hypothesis 2: The B+MEL treatment combination will be associated with improvements in measures of verbal memory, executive functioning, and speed of information processing pre- to post-treatment.

Specific Aim 3 (exploratory aim): To assess neuroimaging changes in fMRI resting state functional connectivity in outpatients with post-TBI depression treated with the B+MEL combination.

Hypothesis 3: The B+MEL treatment combination will show pre- to post-treatment resting state functional connectivity increases within the frontoparietal control network (implicated in cognitive control of attention), decreases within the default network (implicated in internally oriented and self-referential thought), and decreases between the frontoparietal control network and the default network.

Being tested
Buspirone, Mealatonin
Medical subject headings
Depression, Brain Injuries, Traumatic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BuspironeDrug

    Buspirone 15mg once daily

  • MealatoninDrug

    Melatonin 3mg once nightly

Study groups in NCT04400266
Study groupRoleWhat they receive
Buspirone and MelatoninExperimentalBuspirone 15mg and Melatonin 3mg
Receives: Drug: Buspirone; Drug: Mealatonin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Depression

    Hamilton Depression Rating Scale (HDRS); Min. value: 0; Max, value: 62; Higher number indicates higher severity of symptoms.

    Measured: 6 weeks

Secondary outcomes (1)
  1. Cognition

    NIH-Toolbox Cognition Battery Fluid Cognition Composite Score

    Measured: 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 May 2020
  2. Study start1 Aug 2020
  3. Primary completion31 Jul 2028 (estimated)
  4. Study completion31 Jul 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
This is a single-arm, open-label study of the Buspirone and Melatonin combination administered over 6 weeks.
Masking
None (open label)
Enrolment
10 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04400266
Sponsor's protocol ID
2019P003783
Status last verified
May 2026
First submitted
19 May 2020
Last updated
6 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Buspirone and Mealatonin in people with Depression and Brain Injuries, Traumatic, run by Massachusetts General Hospital at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Kaloyan Tanev (6177267511, ktanev@partners.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Depression (time frame: 6 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2026.

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