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Clinical Trials/ChiCTR2000031360
ChiCTR2000031360Not yet recruitingEarly Phase 1

不同强度光照对双相抑郁患者疗效比较的随机对照研究

上海市浦东新区卫健委面上项目(PW2019A-30)1 site in 1 country120 target enrollmentStarted: April 21, 2020Last updated:

Trial Snapshot

Phase
Early Phase 1
Status
Not yet recruiting
Sponsor
Enrollment
120
Locations
1
Primary Endpoint
汉密尔顿抑郁量表

Study Overview

Brief Summary

探寻及比较治疗双相抑郁的有效光照强度。

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照
Masking
未说明

Eligibility Criteria

Ages
18 to 100 (—)
Sex
All

Inclusion Criteria

  • 诊断为双相抑郁且量表分数符合要求;

Exclusion Criteria

  • 六个月诊断内使用精神活性物质所致精神障碍;
  • 两个月内服用过褪黑素 / 慢性非甾体抗炎药;
  • 有严重自杀观念 / 行为。

Arms & Interventions

Group 1

光照强度为 5000lx

Group 2

光照强度为 10000lx

Outcomes

Primary Outcomes

汉密尔顿抑郁量表

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
上海市浦东新区卫健委面上项目(PW2019A-30)

Study Sites (1)

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