Clinical trials

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Condition / disease
Location
Status: Recruiting

Safety and Efficacy of Psilocybin-assisted Psychotherapy for Demoralization Syndrome in Patients Diagnosed With Advanced Stage Cancer

Demoralization syndrome is frequently present in palliative care and oncology patients. In particular, up to a third of patients diagnosed with cancer will experience demoralization due to their illness. The relevance of demoralization syndrome in oncology is tied to this syndrome's association with other mental health ailments such as depression, anxiety, suicidal ideation, and quality of life. Unfortunately, so far no pharmacological strategy has been devised for demoralization, and only a few psychotherapeutic approaches have been trialed in this population, though no psychotherapeutic treatments have been tested for demoralization specifically. The new wave of psychedelic research has been showing encouraging results in a broad spectrum of psychiatric diagnosis, including depression and anxiety in patients diagnosed with cancer and other life-threatening diseases. To date, no clinical trials have been published in which the potential therapeutic effects of psychedelics are explored for the treatment of demoralization syndrome. The aim of this open label pilot study is to assess the safety and efficacy of psilocybin-assisted psychotherapy as a treatment for demoralization syndrome in patients diagnosed with cancer. Fifteen participants between the ages of 18 to 70 years with advanced stage cancer and demoralization syndrome will be enrolled in a treatment program which will include 6 psychotherapeutic sessions and one psilocybin (25 mg) dosing session. Our outcome of interest will be a decrease in demoralization, as measured by the Demoralization Scale at baseline and at the end of the study, and adverse events registration. Other measures of interest include Hamilton Depression Rating Scale, Hamilton Anxiety Rating Scale, and the Columbia Suicide Severity Rating Scale. Those patients with partial response a month after the psilocybin intervention will be offered the possibility of a second psilocybin 25 mg dosing session.

Participants needed: 15
Trial details
Phase: Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: Gustavo VazquezUpdated: Mar 18, 2026Locations: 1
Eligibility criteria

Patients diagnosed with advanced stage cancer (stages 3 and 4) [+5]

Condition impairing oral intake or digestive absorption. [+17]

Status: Recruiting

IV Ketamine vs. IN Esketamine for MDD TRD

The goal of this observational study is to learn about the comparative acute effects of ketamine vs esketamine in participants over the age of 18 for the treatment of their severe depression and suicidal ideations. Participants are already taking antidepressants and/or antipsychotics as part of their regular medical care for depression,

Participants needed: 80
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Gustavo VazquezUpdated: Jul 10, 2024Locations: 1Duration: 4 Weeks
Eligibility criteria

Adult outpatients (18-75 years old) with unipolar depression experiencing major...

Individuals with psychosis, main diagnosis of personality disorder, uncontrolled...