D-Beta hydroxybutyrate Clinical Study

Phase 1

Recruiting

• Conditions: Depression

• Registration Number: JPRN-jRCTs061230063
• Lead Sponsor: Iwata Masaaki

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-09-29
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

1) 20 years old above male or female
2) Patient who have a diagnosis of depression based on the Diagnostic and Statistical Manual of Mental Disorders (5th Edition) (DSM-5) at the start of screening visit and are attending outpatient clinic
3) Patient must administer less than 2 antidepressant with optimum dose within 28 days of enrollment, and must be stable of depression symptom and meet the depression symptom severity (MADRS total score greater than or equal to 22) at the enrollment.
4) If the patient has received sleeping or anxiolytic medications (including those taken by tonics) in the 14 days prior to the start of the double-blind period, the dosage and administration must not have been changed.
5) Patient who have a regular diet
6) Patient must be medically stable on the basis of assessment and observation performed in the screening visit
7) Patient give informed consent

Exclusion Criteria

1) Patient with moderate or higher infection
2) Patient with is drug addic
3) Patient have history of suicidal ideation or suicide attempt
4) Patient who administered anti-inflammatory drug, immune-suppressing drug,SGLT2hibitor or steroid
5) Patient with malignancy
6) Patient with severe organ disorder (cardiovascular disturbanc
7) Patient with diabetes
8) Patient with dementia or sychiatric disease other than depression
9) Patient who have a carbohydrate-restricted diet
10) Patients requiring potassium intake restriction
11) Subject who do not agree to refrain from excessive exercise during the study drug administration
12) Patient who are preg nant or nursing or who desire to become pregnant during the study period. Patients who or whose partners are unwilling to agree to practice appropriate contraception during the study period
13) Patient who had other study drug
14) Patients deemed by the principal investigator to be ineligible for inclusion.

Study & Design

• Study Type: Interventional
• Study Design: Not specified