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Completed

NCT Number: NCT00774813

Nexalin Therapy for the Treatment of Depressive Symptoms

The primary objectives of this Phase II study are to demonstrate the safety of Nexalin Therapy and to investigate the efficacy of Nexalin Therapy.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Leningrad Regional Center of Addiction, Saint Petersburg, Vsevolozhsky District, Russia

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About this study

This randomized, double-blind, placebo-controlled, multi-center trial has 3 different treatment arms.

Study Tools:

  • Hamilton Depression Rating Scale (HAM-D21)
  • Clinical Global Impressions (CGI)
  • Montgomery-Asberg Depression Rating Scale (MADRS)
  • Beck's Depression Inventory
  • Hamilton Anxiety Rating Scale (HAM-A)
  • Hospital Anxiety and Depression Scale (HADS)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with mild to moderate depression episode, based on the HAM-D21 Rating Scale (10-13 = mild; 14-17 = mild to moderate)
  • Diagnosed with mild to moderate depression episode based on ICD-10 Diagnostic Guidelines
  • Is willing and able to spend 4 weeks as a hospital inpatient
  • Is willing and able to return to the clinic during follow-up period

Exclusion criteria

  • A HAM-D21 Rating Scale of <10 or >17
  • Diagnosed outside of mild to moderate depression episode range based on the ICD-10 Diagnostic Guidelines
  • Unable to complete wash-out interval without taking antidepressants or psychotropic medications
  • Is pregnant or may be pregnant
  • Sensitivity to electrodes and/or their conductive gels or adhesives
  • Break in skin integrity at the areas of electrode placement
  • Currently taking immune suppressing drugs or suspected use of narcotics
  • Presence of any implanted electronic devices, cardiac stimulator, or pacemaker
  • History of brain injury, including seizures, epilepsy, stroke, tumor of central nervous system, or hydrocephalus
  • History of heart attacks, congestive heart failure, or uncontrolled hypertension
  • History of schizophrenia or manic-depressive syndrome

Treatment and study plan

Nexalin 1.3mA Device

Device
  • 3 treatment cycles (cycle is 5 daily treatments, followed by 2 days off)
  • Daily receipt of placebo antidepressant

Other names: Nexalin Device

Nexalin 15mA device

Device
  • 3 treatment cycles (cycle is 5 daily treatments, followed by 2 days off)
  • Daily receipt of a placebo antidepressant

Other names: Nexalin Device

placebo device and Citalopram

Drug
  • 3 treatment cycles (cycle is 5 daily treatments, followed by 2 days off)
  • Daily receipt of a a SSRI (Citalopram or similar)

Other names: Nexalin Device

Primary outcomes

  1. Hamilton Depression Rating Scale (HAM-D21)

    Time frame: Screening; Baseline; Treatments 5, 10, & 15; Follow-up Weeks 2, 4, 8, & 12

Secondary outcomes

  1. Clinical Global Impression (CGI)

    Time frame: Screening; Baseline; Treatments 5, 10, & 15; Follow-up Weeks 2, 4, 8, & 12

  2. Montgomery-Asberg Depression Rating Scale (MADRS)

    Time frame: Screening; Baseline; Treatments 5, 10, & 15; Follow-up Weeks 2, 4, 8, & 12

  3. Beck's Depression Inventory

    Time frame: Screening; Baseline; Treatments 5, 10, & 15; Follow-up Weeks 2, 4, 8, & 12

  4. Hamilton Anxiety Rating Scale (HAM-A)

    Time frame: Screening; Baseline; Treatments 5, 10, & 15; Follow-up Weeks 2, 4, 8, & 12

  5. Hospital Anxiety and Depression Scale (HADS)

    Time frame: Screening; Baseline; Treatments 5, 10, & 15; Follow-up Weeks 2, 4, 8, & 12

  6. Medication Usage Log

    Time frame: Every visit

  7. Adverse Event Log

    Time frame: Every visit

Sponsors and collaborators

Lead sponsor

Kalaco Scientific, Inc.

Industry

Registry information

Official study title

Phase II Study Using Nexalin Therapy for the Treatment of Depressive Symptoms Associated With Mild to Moderate Depression Episodes

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Oct 17, 2008
Registry last updated
Oct 17, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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