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A Clinical Study on the Effects of Inhalation of Volatile Oil of Cang-Ai Via the Nose on Patients With Depression

Primary Purpose

Depressive Disorder, Mental Disorder in Adolescence

Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Volatile Oil of Cang-Ai
Bergamot essential oils
Sponsored by
Jieqiong Cui
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder focused on measuring Aromatic Herbs, Volatile oils, Inhalation via the nose

Eligibility Criteria

6 Years - 28 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Meeting the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnostic criteria for depressive episodes.

    • Beck Depression Scale >10; 24-item Hamilton Depression Scale (HAMD) score >20

      • Healthy sense of smell, no allergic diseases, respiratory diseases, age 16-40 years, male or female.

        • No use of antidepressants and other psychiatric drugs or physiotherapy such as electroconvulsive shock or transcranial magnetic stimulation (TMS) for at least 1 week prior to the intervention ⑤All subjects volunteered to participate and signed an informed consent form after approval by the hospital's ethics committee

Exclusion Criteria:

  • History of schizophrenia, alcohol and drug dependence strictly excluded ②Depression with a history of organic brain disease and endocrine disorders or secondary to other psychiatric disorders

    • Score >3 on the Hamilton Depression Inventory for Suicide ④Pregnant and breastfeeding women with a history of manic or hypomanic episodes ⑤Family history of monophasic or bipolar disorder

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Cang-Ai Group

    Bergamot group

    Arm Description

    The test group inhaled the volatile oil of Cang-Ai at a concentration of 1% by inhalation once a day for 30 minutes

    The control group inhaled the bergamot essential oils at a concentration of 1% by inhalation once a day for 30 minutes

    Outcomes

    Primary Outcome Measures

    Change from functional near-infrared spectroscopy(fNIRS) at 28 days
    Functional near-infrared spectroscopy to measure changes in the relative concentrations of Oxy-Hb and Deoxy-Hb in the cerebral cortex (prefrontal and temporal lobes)
    Change from functional near-infrared spectroscopy(fNIRS) at 28 days
    Functional near-infrared spectroscopy to measure changes in the relative concentrations of Oxy-Hb and Deoxy-Hb in the cerebral cortex (prefrontal and temporal lobes)
    24-item Hamilton Depression Inventory scores
    The following severity ranges for the HAMD: no depression (0-7); mild depression (8-16); moderate depression (17-23); and severe depression (≥24)
    24-item Hamilton Depression Inventory scores
    The following severity ranges for the HAMD: no depression (0-7); mild depression (8-16); moderate depression (17-23); and severe depression (≥24)

    Secondary Outcome Measures

    Change from blood pressure
    Patients' blood pressure will be measured by a blood pressure monitor
    Change from blood pressure at 28 days
    Patients' blood pressure will be measured by a blood pressure monitor
    Change from heart rate
    Patients' heart rate will be measured by a heart rate monitor
    Change from heart rate at 28 days
    Patients' heart rate will be measured by a heart rate monitor

    Full Information

    First Posted
    January 24, 2022
    Last Updated
    October 19, 2022
    Sponsor
    Jieqiong Cui
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05251779
    Brief Title
    A Clinical Study on the Effects of Inhalation of Volatile Oil of Cang-Ai Via the Nose on Patients With Depression
    Official Title
    A Clinical Study on the Effects of Inhalation of Volatile Oil of Cang-Ai Via the Nose on Patients With Depression
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 1, 2022 (Anticipated)
    Primary Completion Date
    December 1, 2022 (Anticipated)
    Study Completion Date
    December 1, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Jieqiong Cui

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In this study, 60 depressed patients who meet the criteria will randomly be divided into a test group and a control group, with 30 patients in each group. The test group will be given Volatile oil of Cang-Ai (hereafter referred to as CAVO) for inhalation and the control group will be given Bergamot for inhalation. The observation indicators are that after one and two sessions of the intervention, the patients' blood pressure, heart rate, depression scale scores, and changes in functional near-infrared spectroscopy(fNIRS). This randomized controlled trial will be used to look at the clinical efficacy of CAVO in patients with depression.
    Detailed Description
    Depression is a common psychiatric disorder characterised by persistent depressed mood, loss of interest and feelings of helplessness. Depression has the highest burden of illness of any mental illness and is the leading cause of disability. Currently, depression is usually treated with antidepressants as the first line of treatment, but because the pathophysiological mechanisms of depression are still unclear, the mechanisms of antidepressant treatment are unknown, and there is no objective way to predict efficacy, depression often requires multiple "trial and error treatments" before an effective treatment plan can be determined. Chemically synthesised drugs are widely used to treat depression, but side effects have become a bottleneck to their long-term use. As a result, natural products from medicinal plants, such as Essential oils or Volatile oils, have become research targets for the development of new drugs. Volatile oil of Cang-Ai is a component extracted from aromatic Chinese herbs such as Atractlodis Rhizoma, Herba Agastaches, Flos Caryophylli, which is commonly used clinically in the treatment of mood disorders. This study will use a randomised controlled study method. 60 patients with depression who attended the First Affiliated Hospital of Yunnan University of Traditional Chinese Medicine from March 2022 to September 2022 will be recruited. They will be randomly divided into a trial group and a control group, 30 patients in each group. The test group will be given Volatile oil of Cang-Ai for inhalation and the control group will be given Bergamot for inhalation. Ultimately, a number of indicators will be tested to assess the clinical efficacy of the volatile oil of Cang-Ai.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Depressive Disorder, Mental Disorder in Adolescence
    Keywords
    Aromatic Herbs, Volatile oils, Inhalation via the nose

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Cang-Ai Group
    Arm Type
    Experimental
    Arm Description
    The test group inhaled the volatile oil of Cang-Ai at a concentration of 1% by inhalation once a day for 30 minutes
    Arm Title
    Bergamot group
    Arm Type
    Active Comparator
    Arm Description
    The control group inhaled the bergamot essential oils at a concentration of 1% by inhalation once a day for 30 minutes
    Intervention Type
    Drug
    Intervention Name(s)
    Volatile Oil of Cang-Ai
    Other Intervention Name(s)
    CAVO
    Intervention Description
    The test group will be given Volatile oil of Cang-Ai (hereafter referred to as CAVO) for inhalation
    Intervention Type
    Drug
    Intervention Name(s)
    Bergamot essential oils
    Other Intervention Name(s)
    Citrus bergamia
    Intervention Description
    The control group will be given Bergamot essential oils for inhalation.
    Primary Outcome Measure Information:
    Title
    Change from functional near-infrared spectroscopy(fNIRS) at 28 days
    Description
    Functional near-infrared spectroscopy to measure changes in the relative concentrations of Oxy-Hb and Deoxy-Hb in the cerebral cortex (prefrontal and temporal lobes)
    Time Frame
    At the end of Cycle 1 (each cycle is 14 days)
    Title
    Change from functional near-infrared spectroscopy(fNIRS) at 28 days
    Description
    Functional near-infrared spectroscopy to measure changes in the relative concentrations of Oxy-Hb and Deoxy-Hb in the cerebral cortex (prefrontal and temporal lobes)
    Time Frame
    At the end of Cycle 2 (each cycle is 14 days)
    Title
    24-item Hamilton Depression Inventory scores
    Description
    The following severity ranges for the HAMD: no depression (0-7); mild depression (8-16); moderate depression (17-23); and severe depression (≥24)
    Time Frame
    At the end of Cycle 1 (each cycle is 14 days)
    Title
    24-item Hamilton Depression Inventory scores
    Description
    The following severity ranges for the HAMD: no depression (0-7); mild depression (8-16); moderate depression (17-23); and severe depression (≥24)
    Time Frame
    At the end of Cycle 2 (each cycle is 14 days)
    Secondary Outcome Measure Information:
    Title
    Change from blood pressure
    Description
    Patients' blood pressure will be measured by a blood pressure monitor
    Time Frame
    At the end of Cycle 1 (each cycle is 14 days)
    Title
    Change from blood pressure at 28 days
    Description
    Patients' blood pressure will be measured by a blood pressure monitor
    Time Frame
    At the end of Cycle 2 (each cycle is 14 days)
    Title
    Change from heart rate
    Description
    Patients' heart rate will be measured by a heart rate monitor
    Time Frame
    At the end of Cycle 1 (each cycle is 14 days)
    Title
    Change from heart rate at 28 days
    Description
    Patients' heart rate will be measured by a heart rate monitor
    Time Frame
    At the end of Cycle 2 (each cycle is 14 days)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Years
    Maximum Age & Unit of Time
    28 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Meeting the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnostic criteria for depressive episodes. Beck Depression Scale >10; 24-item Hamilton Depression Scale (HAMD) score >20 Healthy sense of smell, no allergic diseases, respiratory diseases, age 16-40 years, male or female. No use of antidepressants and other psychiatric drugs or physiotherapy such as electroconvulsive shock or transcranial magnetic stimulation (TMS) for at least 1 week prior to the intervention ⑤All subjects volunteered to participate and signed an informed consent form after approval by the hospital's ethics committee Exclusion Criteria: History of schizophrenia, alcohol and drug dependence strictly excluded ②Depression with a history of organic brain disease and endocrine disorders or secondary to other psychiatric disorders Score >3 on the Hamilton Depression Inventory for Suicide ④Pregnant and breastfeeding women with a history of manic or hypomanic episodes ⑤Family history of monophasic or bipolar disorder

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    The original data from each eligible study. including de-identified demographic information for each participant such as age, sex, nature of their health condition, as well as information about treatments or tests received and outcomes observed
    IPD Sharing Time Frame
    After Dec 2022
    IPD Sharing Access Criteria
    Sharing with researcher for Meta-analysis

    Learn more about this trial

    A Clinical Study on the Effects of Inhalation of Volatile Oil of Cang-Ai Via the Nose on Patients With Depression

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