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Wuling Powder for the Treatment and Underlying Mechanism of Depressive Symptoms in Patients With Parkinson's Disease

Primary Purpose

Antidepressive Agents

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Wuling Powder
Placebo
Sponsored by
Beijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Antidepressive Agents focused on measuring Parkinson's disease, Depression, Wuling Powder

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis of idiopathic Parkinson's disease according to the 2015 MDS(Movement Disorder Society)-PD criterion
  2. Hoehn-Yahr stage: 1-3
  3. Under steady therapy of antiparkinsonian drugs for at least 28 days
  4. HAMD≥13
  5. MMSE(Mini-Mental State Examination)≥24
  6. Neither use antidepressant drugs nor antipsychotic drugs within 4 weeks
  7. Signed informed consent

Exclusion Criteria:

  1. Have other psychotic symptoms
  2. Suicide ideation or behavior
  3. Severe cognitive impairment,chronic organs failure,malignant tumors
  4. Glutamic-pyruvic transaminase or glutamic oxalacetic transaminase≥1.5 times of the high normal range or white blood cell<4*10^9/L or serum creatinine>84umol/L
  5. Pregnancy or lactation period
  6. Participant in other trials or have taken other experimental drugs within 90 days
  7. Allergic to fungal food or fungal drugs

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Wuling Powder Group

    Placebo Group

    Arm Description

    Take Wuling Powder 3 times a day,3 pills each time for 12 weeks

    Take placebo drug which cannot be distinguished from the experimental drug 3 times a day,3 pills each time for 12 weeks

    Outcomes

    Primary Outcome Measures

    the change of depression from baseline to 12 weeks
    the change of depression from baseline to 12 weeks,as assessed with the use of HAMD(Hamilton Depression Scale)

    Secondary Outcome Measures

    Full Information

    First Posted
    June 20, 2017
    Last Updated
    June 20, 2017
    Sponsor
    Beijing Hospital
    Collaborators
    Tongji Hospital, Shanghai Tong Ren Hospital, The First Hospital of Hebei Medical University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03195231
    Brief Title
    Wuling Powder for the Treatment and Underlying Mechanism of Depressive Symptoms in Patients With Parkinson's Disease
    Official Title
    Wuling Powder for the Treatment and Underlying Mechanism of Depressive Symptoms in Patients With Parkinson's Disease: a Randomised, Double-blind, Placebo-controlled Trial.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 25, 2017 (Anticipated)
    Primary Completion Date
    December 15, 2019 (Anticipated)
    Study Completion Date
    January 15, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Beijing Hospital
    Collaborators
    Tongji Hospital, Shanghai Tong Ren Hospital, The First Hospital of Hebei Medical University

    4. Oversight

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

    5. Study Description

    Brief Summary
    Depression is one of the most important nonmotor features of idiopathic PD(Parkinson's disease )which may not just interfere with the motor symptoms of PD but can also cause immense personal suffering as well as decreased quality of life with increased disability and caregiver burden. However,there is little hard evidence to guide clinical treatment. Although some newer dopamine agonists also have antidepressive effect, the use of tricyclic or nontricyclic antidepressants is frequently required.However, the side-effects of these agents may also worsen some preexisting nonmotor problems in PD. Wuling powder is a Chinese medicine which is made by cultivating Xylariasp mycelium using submerged fermentation technology. Xylariasp is the fungus sclerotia which grow in termite nests. Wuling powder is mainly used to soothe nerves and anti-insomnia in clinical. The antidepressant effect of Wuling powder has been confirmed in clinical, but not in the patients of Parkinson's disease. Therefore, the investigators design a randomized, double-blind, placebo-controlled study to evaluate the antidepressant effect of Wuling powder in PD patients and its underlying mechanism.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Antidepressive Agents
    Keywords
    Parkinson's disease, Depression, Wuling Powder

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Wuling Powder Group
    Arm Type
    Experimental
    Arm Description
    Take Wuling Powder 3 times a day,3 pills each time for 12 weeks
    Arm Title
    Placebo Group
    Arm Type
    Placebo Comparator
    Arm Description
    Take placebo drug which cannot be distinguished from the experimental drug 3 times a day,3 pills each time for 12 weeks
    Intervention Type
    Drug
    Intervention Name(s)
    Wuling Powder
    Intervention Description
    Patients of Wuling Group are instructed to take Wuling Powder 3 times a day and 3 pills each time for 12 weeks.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    Patients of Placebo Group are instructed to take placebo drug 3 times a day and 3 pills each time for 12 weeks.
    Primary Outcome Measure Information:
    Title
    the change of depression from baseline to 12 weeks
    Description
    the change of depression from baseline to 12 weeks,as assessed with the use of HAMD(Hamilton Depression Scale)
    Time Frame
    12 weeks after treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of idiopathic Parkinson's disease according to the 2015 MDS(Movement Disorder Society)-PD criterion Hoehn-Yahr stage: 1-3 Under steady therapy of antiparkinsonian drugs for at least 28 days HAMD≥13 MMSE(Mini-Mental State Examination)≥24 Neither use antidepressant drugs nor antipsychotic drugs within 4 weeks Signed informed consent Exclusion Criteria: Have other psychotic symptoms Suicide ideation or behavior Severe cognitive impairment,chronic organs failure,malignant tumors Glutamic-pyruvic transaminase or glutamic oxalacetic transaminase≥1.5 times of the high normal range or white blood cell<4*10^9/L or serum creatinine>84umol/L Pregnancy or lactation period Participant in other trials or have taken other experimental drugs within 90 days Allergic to fungal food or fungal drugs
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Xin Wang
    Phone
    +8613661174001
    Email
    wangxinannie@126.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Wen Su
    Organizational Affiliation
    Beijing Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Wuling Powder for the Treatment and Underlying Mechanism of Depressive Symptoms in Patients With Parkinson's Disease

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