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The effect of levothyroxine on ECT Induced Memory Impairment in bipolar patients

The effect of levothyroxine on ECT Induced Memory Impairment in bipolar patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015071012018N3
Enrollment
48
Registered
2016-09-16
Start date
2016-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

BIPOLAR affective disorder. Bipolar affective disorder

Interventions

Intervention 1: tablet levothyroxine 0.1 mg daily fasting during ECT treatment. Intervention 2: Tablet Placebo(similar Levothyroxine) daily Fasting during ECT treatment.
Treatment - Drugs
tablet levothyroxine 0.1 mg daily fasting during ECT treatment
Tablet Placebo(similar Levothyroxine) daily Fasting during ECT treatment

Sponsors

Qazvin University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Diagnosis of bipolar disorder based on SCID questionnaire that its persian validity and reliability is confirmed??Presence of ECT indication is under recommendation of psychiatrist?Age between 18-64?consent letter of patient's parents.Exclusion criteria:Any contraindication of levothyroxine?Comorbidity of substance or alcohol dependence?Any organic brain disorder or mental retardation (based on history, physical exam and patient's records) or any cognitive impairment(MMSE<23) at begining of study?ECT less than 6 session?ECT induced delirium?not using at least one of standard mood stabilizers (sodium valproate ,lithium carbonate or carbamazepin)?use more than one of standard mood stabilizers (sodium valproate ,lithium carbonate or carbamazepin)?use more than one convulsion in ECT in at least half of sessions?siezure duration below 15 second in more than half of sessions?siezure duration higher thant 3 minutes in even one session?

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Memory impairment. Timepoint: Baseline and Then two weeks after completion of therapy ???. Method of measurement: wecsler memory tese.

Secondary

MeasureTime frame
Cognitin state. Timepoint: Baseline and Then two weeks after completion of therapy ???. Method of measurement: mmse.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Seyed Majid Hoseiny Hoshyar

Qazvin University of Medical Science

majidhooshyar@yahoo.com+98 28 3336 9923

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026