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Completed

NCT Number: NCT01655030

Creatine Monohydrate as Adjuvant Therapy for Bipolar Depression

The purpose of this study is to determine whether creatine monohydrate is effective as an adjuvant treatment for bipolar depression.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Psychiatry - HC-FMUSP

São Paulo, 01060-970, Brazil

About this study

Bipolar Depression is associated with high rates of disability and increased mortality. Despite its major negative impact, treatment of Bipolar Depression is still controversial and only partially efficacious, with over half of patients not responding adequately to available treatment. In this context, the use of drugs that modulate energy metabolism has been proposed as promising new option as treatment strategies for bipolar depression. The aim of our proposed study is to perform a 6-week randomized, double-blind, placebo-controlled clinical trial of creatine monohydrate as an adjuvant treatment for bipolar depression.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Individuals eligible for the study will be adults aged 18 to 60 years of age who met DSM-IV criteria assessed by the SCID (Structural Clinical Interview for DSM-IV) for type I bipolar disorder, current episode depressed.
  • Patients who have scored > 19 on the Montgomery-Asberg Depression Rating Scale (MADRS) will be included, although more than two weeks of treatment with lithium (serum level> 0.8 mEq / L), valproate (serum levels> 50 mg / L) or quetiapine (300-600mg/dia dose) or drug combination.
  • Antipsychotics, anticonvulsants, benzodiazepines, and thyroid supplementation will be allowed if the dose has remained stable over the past two weeks.
  • Antidepressants will be allowed if the dosage has remained stable for 4 weeks.

Exclusion criteria

  • Subjects with substance abuse within 2 weeks before inclusion or substance dependence up to 2 months will not be included.
  • Other exclusion criteria will be:
  • diagnosis of schizophrenia,
  • dementia,
  • delirium,
  • epilepsy,
  • mental retardation,
  • clinically unstable medical illnesses,
  • preexisting renal disease,
  • history of hypersensibility to creatine.
  • Not included are individuals at high risk for suicidal or homicidal behavior or self-mutilation will not be included.
  • Women with gestational potential can only be included if they are using reliable contraception.

Treatment and study plan

Creatine Monohydrate

Dietary Supplement

Placebo

Dietary Supplement

Primary outcomes

  1. MADRS (Montgomery-Asberg Depression Rating Scale)

    Time frame: 6 weeks

    change of score on the Montgomery-Asberg Depression Rating Scale

Secondary outcomes

  1. HDRS-17 (Hamilton Depression Rating Scale - 17-item version)

    Time frame: 6 weeks

    change of score on the Hamilton Depression Rating Scale - 17-item version

Other outcomes

  1. CGI (Clinical Global Impressions Scale) - Severity and Improvement

    Time frame: 6 weeks

    change of score on the Clinical Global Impressions Scale

  2. YMRS (Young Mania Rating Scale)

    Time frame: 6 weeks

    change of score on the Young Mania Rating Scale

Sponsors and collaborators

Lead sponsor

University of Sao Paulo

Other

Registry information

Official study title

A Double-Blind, Randomized, Placebo-Controlled Clinical Trial to Evaluate the Efficacy of Creatine Monohydrate as Adjunctive Therapy for Bipolar Depression

Important dates

Study start
2012
Primary completion
2016
Study completion
2016
First posted
Aug 1, 2012
Registry last updated
Dec 5, 2023

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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