ITMCTR2000004186Recruiting未知
A protocol of randomized controlled trial for Modified Xiaoyao Powder in the treatment of chronic obstructive pulmonary disease combined mild to moderate depression
Hospital of Chengdu University of Traditional Chinese Medicine0 sitesStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional study
Eligibility Criteria
- Ages
- 18 to 65 (—)
- Sex
- All
Inclusion Criteria
- •1. Aged 18 to 65 years men and women;
- •2. Patients who had received a diagnosis of COPD combined mild to moderate depression (HAMD-17 score 7 to 24) and meet the syndrome of stagnation of liver qi of depression;
- •3. The course of depression does not exceed 3 months;
- •4. The patients has not taken antidepressants in the past 1 month;
- •5. Agree to participate and sign an informed consent form.
Exclusion Criteria
- •1. A history of a suicide attempt treament-resistant depression, and familial mental illness;
- •2. Had a recent history of other acute or chronic significant clinical manifestations medical conditions;
- •3. A history of bipolar disorder, schizophrenia, or schizo affective disorder;
- •4. Patients who cannot actively cooperate with the treatment.
Investigators
Similar Trials
Not yet recruiting
Phase 1
A Randomized Controlled Trial Study Protocol of Modified Mahuang-Fuzi-Xixin Decoction in the Treatment of Patients with Mild Bronchial Asthma During Acute ExacerbatioBronchial AsthmaITMCTR2000003457Affiliated Hospital of Chengdu University of traditional Chinese Medicine
Completed
Not Applicable
Study protocol for a randomized controlled trial of the effectiveness providing information on childbirth and postnatal period to partners of pregnant womePaternal depressionJPRN-UMIN000021475ational Center for Child Health and Development577
Completed
Phase 4
Study protocol for a randomized clinical trial of a continuous butylscopolamine infusion versus a placebo in patients with a renal colic not responding to oral NSAIDs10046708urolithiasisNL-OMON47573HagaZiekenhuis128
Withdrawn
Not Applicable
Study protocol for a randomised clinical trial comparing TREPP versus Lichtenstein*s technique in Inguinal hernia patientsInguinal hernia10040795NL-OMON45767Medisch Centrum Leeuwarden750
Active, not recruiting
Unknown
Protocol for a Randomised Controlled Trial to evaluate psychosocial and behaviour impact of providing personalised risk scores for melanomaCancer - Malignant melanomamelanomaACTRN12624000707561The University of Queensland145