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Completed

NCT Number: NCT01309776

Comparison of Tianeptine Versus Escitalopram Patients Major Depressive Disorder

The primary object of this study is to confirm the superiority of tianeptine compared to escitalopram on effects that improves subjective and objective cognitive impairments in patients suffering from major depressive disorder.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Inje University Paik Hospital, Goyang, South Korea

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About this study

Along with depressive symptoms, subjective and objective cognitive impairments are frequently complained by the patients with major depressive disorder. Tianeptine acts on glutamate system and is known as a promising drug for improving cognitive impairment.

The present study aims to confirm the superiority of tianeptine compared to escitalopram on effects that improves subjective and objective cognitive impairments after a 12-week treatment in patients suffering from major depressive disorder.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients fulfilling DSM-IV-TR(American Psychiatric Association, 4thedition, 2000) criteria for Major Depressive Disorder diagnosis
  • The male or female patients aged more than 40 years
  • Patients able to hand in written informed consent before his/her participation in this clinical study
  • Women of childbearing potential with negative pregnancy test during screening phase and entire study period (during entire study period, able to clearly agree with effective contraception such as contraceptive pill, progesterone injection, levonorgestrel implant, estrogen ring, transdermal contraceptive agent, intra-uterine contraceptive device, sterilization operation of husband, and double contraceptive method (e.g. combination of condom, pessary, spermicide, etc. ))
  • Patients who have subjective cognitive impairment, or who have objective cognitive impairment (MMSE ≤26) without subjective cognitive impairment
  • HAM-D(17-items) total score ≥ 16

Exclusion criteria

  • Patients meeting more than one following patient characteristics
  • Patients fulfilling DSM-IV-TR current or past diagnosis of any psychiatric disorders other than major depressive disorder (i.e. manic or hypomanic episode, schizophrenia, delirium, dementia, eating disorder, obsessive-compulsive disorder, panic disorder, post-traumatic stress disorder, major depressive disorder with psychotic features, mental retardation, organic brain disorder, or psychiatric disorders due to general medical condition, according to DSM-IV-TR)
  • Patients with any substance-related disorder (excluding nicotine) within the past 12 months, as defined in DSM-IV-TR
  • Patients with a history or presence of any neurological disorders (e.g. multiple sclerosis, seizure, etc.)
  • Patients with any axis II disorder that prone to interfere with the evaluation of the study
  • Patients with a history or presence of any hypersensitivity to tianeptine, escitalopram or other drugs
  • Patients who receive formal psychotherapy (e.g. cognitive behavioral therapy, insight-oriented psychoanalysis, interpersonal therapy, etc.) and who have a plan for getting psychotherapy
  • Patients with any clinically significant abnormality (e.g. hepatic failure, renal failure, cardiovascular disorder, respiratory disorder, gastrointestinal disorder, endocrine disorder, neurological disorder, inflammatory disorder, neoplasm, metabolic disorder, etc.)
  • Patients who have abnormal ECG and a significant disease according to the investigator's judgment
  • Patients with any chronic liver or kidney disease
  • Patients with a family history of long QT syndrome
  • Patients previously not responders to tianeptine or escitalopram in the treatment of major depressive disorder
  • Patients who have a suicide risk according to the investigator's judgment

Treatment and study plan

Tianeptine

Drug

week1 : 25mg/day q.d., week2: 37.5mg/day b.i.d. (12.5mg 1T, 12.5mg 2T

Other names: Stablon

Escitalopram

Drug

week1 : 5mg/day q.d., week2: 10mg/day q.d.

Primary outcomes

  1. Changes in Hamilton Rating Scale for Depression(HAM-D)score from baseline

    Time frame: followed up to 2,4,8,12 weeks from baseline

  2. Changes in Korean version-California Verbal Learnign Test(K-CVLT) total score from baseline

    Time frame: followed up to 4,8,12 weeks from baseline

  3. Changes in Visual Continuous Performance Test(CPT) total score from baseline

    Time frame: followed up to 4,8,12 weeks from baseline

  4. Changes in Raven Progressive Matrices(RPM) total score from baseline

    Time frame: followed up to 4,8,12 weeks from baseline

Secondary outcomes

  1. Changes in Hamilton Rating Scale for Anxiety(HAM-A) score from baseline

    Time frame: followed to 2,4,8,12 weeks from baseline

  2. Changes in Clinical Clinical Global Impression- improvement(CGI-I)

    Time frame: followed to 2,4,8,12 weeks from baseline

  3. Change in Response Rate from baseline

    Time frame: followed to 12 weeks from baseline

  4. Change in Mini-Mental status examination(MMSE) total score from baseline

    Time frame: followed to 4,8,12 weeks from baseline

  5. Change in Sexual Function Scale

    Time frame: followed to 2,4,8,12 weeks from baseline

  6. Change in Clinical Global Impression- severity(CGI-S)

    Time frame: followed to 2,4,8,12 weeks from baseline

  7. Change in Remission Rate from baseline

    Time frame: followed to 12 weeks from baseline

Sponsors and collaborators

Lead sponsor

Samsung Medical Center

Other

Registry information

Official study title

Comparison of Tianeptine Versus Escitalopram for the Treatment of Depression and Cognitive Impairment in Patients With Major Depressive Disorder: A Randomized, Multicenter, Open-label Study

Acronym: CAMPION

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Mar 7, 2011
Registry last updated
Jan 25, 2013

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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