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Efficacy and possible mechanism of prazosin combined with prazosin in the treatment of trauma related depression

Effect of combined prazosin on trauma related depression and its effect on glucose metabolism

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063642
Enrollment
Unknown
Registered
2022-09-13
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

major depressive disorder

Interventions

prazosin group:prazosin
placebo grooup:placebo

Sponsors

Huzhou Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria of dsm-5 for moderate / severe depression and is further verified by mini set clinical interview; (2) Han nationality; Both men and women, aged from 13 to 65; (3) HAMD-21 = 18 points, CGI-S = 3 points; (4) There are childhood (before the age of 17) trauma or recent (within 3 years) traumatic stress events. (5) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Schizophrenic affective psychosis, dysthymia or bipolar depression; Any anxiety disorder was the main diagnosis within 1 year; obsession; Patients with substance abuse or dependence; Personality disorders. (2) Various contraindications covered in the instructions for the use of prazosin, such as: allergy to prazosin, hypotension ( 100bpm), and large blood pressure difference in lying position( ? Systolic blood pressure > 20mmhg, ? Diastolic blood pressure > 10mmhg, or ? Mean arterial pressure > 20mmhg) or other people who are not suitable for this treatment are not included. (3) Pregnant or lactating women; (4) Patients with serious or unstable heart, liver, kidney, endocrine organs, blood, autoimmune diseases and other medical diseases; Patients with epilepsy or other brain organic diseases; Increased intracranial pressure, intractable and refractory hypertension, glaucoma, etc; (5) A serious history of attempted suicide, or there is a high risk of suicide at present, or the HAMD 3rd suicide score = 3; (6) NMDA receptor antagonists such as ketamine have been used in the past; (7) Systematic antipsychotic treatment was received 2 weeks before enrollment; (8) Those who have received electroconvulsive therapy, rTMS therapy or systematic psychotherapy in recent 3 months.

Design outcomes

Primary

MeasureTime frame
Totle score reduction of Hamilton Depression scale-17 items;

Secondary

MeasureTime frame
Montgomery-Asberg Depression Rating Scale;Columbia - suicide severity rating scale questionnaire;Hamilton Anxiety Scale;Clinical general impression scale;Digit Symbol Substitution Test;Perceived Deficit Questionnaire for Depression;QOL-BREF;SHEEHAN DISABILITY SCALE;

Countries

China

Contacts

Public ContactShikai Wang

Huzhou Third People's Hospital

404422688@qq.com13665752769

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026