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Melatonin Treatment for Tardive Dyskinesia in Schizophrenia

Primary Purpose

Tardive Dyskinesia

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Melatonin
Placebo
Sponsored by
Beijing HuiLongGuan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tardive Dyskinesia focused on measuring Tardive Dyskinesia, Schizophrenia, Melatonin, Oxidative Stress, Antioxidant

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. diagnosis of both schizophrenia and TD;
  2. duration of TD symptoms longer than 1 year;
  3. on stable doses of antipsychotic drug for at least 6 months;
  4. between 18 and 70 years of age.

Exclusion Criteria:

  1. comorbid neurological illness other than TD;
  2. if they have received vitamin C or vitamin E within 1 month before the start of the study;
  3. alcohol/drug abuse;
  4. acute, unstable medical condition;
  5. pregnant or breastfeeding female;
  6. use of other antioxidants.

Sites / Locations

  • Beijing HuiLongGuan hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Melatonin, antioxidant, oxidative stress

Placebo

Arm Description

Melatonin is an active treatment for TD.

Placebo look like the active drug, and same dose.

Outcomes

Primary Outcome Measures

the Abnormal Involuntary Movement Scale (AIMS)

Secondary Outcome Measures

the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
the Positive and Negative Syndrome Scale (PANSS)
the Simpson-Angus Scale for extrapyramidal side effects (SAS)

Full Information

First Posted
July 7, 2011
Last Updated
July 10, 2016
Sponsor
Beijing HuiLongGuan Hospital
Collaborators
Stanley Medical Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01391390
Brief Title
Melatonin Treatment for Tardive Dyskinesia in Schizophrenia
Official Title
The Effect of Melatonin Treatment on Tardive Dyskinesia and Oxidative Stress: A Double-Blind Placebo-Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
May 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing HuiLongGuan Hospital
Collaborators
Stanley Medical Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a double-blind, randomized, placebo-controlled trial of melatonin as an add-on therapy to antipsychotics will be performed to examine the effects of melatonin on tardive dyskinesia symptoms and cognitive deficits in 120 patients with established tardive dyskinesia (TD). This study addresses a free radical hypothesis of TD.
Detailed Description
Since it has been proposed that neuroleptic-induced increases in free-radical production may relate to the development of TD, the investigators hypothesize that melatonin, an effective antioxidant, may attenuate the severity of tardive dyskinesia symptoms. Due to increased cognitive deficits in patients with TD and implication of oxidative stress in cognitive impairment, the investigators hypothesize that both cognitive impairment and tardive dyskinesia symptoms may be induced by the same pathophysiological stimulus--oxidative stress. Hence, the investigators further hypothesize that both tardive dyskinesia symptoms and cognitive deficits in patients with TD may be improved by melatonin simultaneously.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tardive Dyskinesia
Keywords
Tardive Dyskinesia, Schizophrenia, Melatonin, Oxidative Stress, Antioxidant

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Melatonin, antioxidant, oxidative stress
Arm Type
Experimental
Arm Description
Melatonin is an active treatment for TD.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo look like the active drug, and same dose.
Intervention Type
Drug
Intervention Name(s)
Melatonin
Other Intervention Name(s)
APRD00742
Intervention Description
10mg/day, 12-week treatment
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
10mg/day, 12-week treatment for TD
Primary Outcome Measure Information:
Title
the Abnormal Involuntary Movement Scale (AIMS)
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
Time Frame
12 weeks
Title
the Positive and Negative Syndrome Scale (PANSS)
Time Frame
12 weeks
Title
the Simpson-Angus Scale for extrapyramidal side effects (SAS)
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of both schizophrenia and TD; duration of TD symptoms longer than 1 year; on stable doses of antipsychotic drug for at least 6 months; between 18 and 70 years of age. Exclusion Criteria: comorbid neurological illness other than TD; if they have received vitamin C or vitamin E within 1 month before the start of the study; alcohol/drug abuse; acute, unstable medical condition; pregnant or breastfeeding female; use of other antioxidants.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lian Y Cao, MD
Organizational Affiliation
Beijing HuiLongGuan Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Beijing HuiLongGuan hospital
City
Beijing
ZIP/Postal Code
100096
Country
China

12. IPD Sharing Statement

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Melatonin Treatment for Tardive Dyskinesia in Schizophrenia

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