Protocol summary
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Study aim
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Determining the effectiveness of oral phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
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Design
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Clinical trial with control group, with parallel groups, blinded, randomized, phase 2 on 70 patients. The rand function of Excel software was used for randomization
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Settings and conduct
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Ibn Sina Hospital of Mashhad will be conducted on 70 patients aged 18-40 with bipolar disorder in the acute phase of mania. The disease was diagnosed based on the diagnostic criteria of DSM-5 and the severity of the symptoms will be evaluated on the day of hospitalization and daily during one week of the start of injectable drug treatments.
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Participants/Inclusion and exclusion criteria
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1. Patients with bipolar disorder in an episode
2. Patients in the age range of 18 to 40
3. Absence of pregnancy and postpartum period
4. Not having medical illness, especially convulsions
Exclusion criteria:
sensitivity to drug treatment
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Intervention groups
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The first group received oral phenytoin with an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose on a weekly basis until the dose of 600 mg.
and the second group will receive oral sodium valproate at a dose of 20 mg/kg daily for two weeks.
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Main outcome variables
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Patients' symptoms based on daily visits and YMRS, CGI tests
General information
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Reason for update
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Conversion of injectable phenytoin to oral phenytoin
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Acronym
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IRCT registration information
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IRCT registration number:
IRCT20101130005280N61
Registration date:
2023-03-23, 1402/01/03
Registration timing:
registered_while_recruiting
Last update:
2024-06-14, 1403/03/25
Update count:
2
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Registration date
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2023-03-23, 1402/01/03
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Registrant information
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Recruitment status
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Recruitment complete
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Funding source
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Expected recruitment start date
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2023-03-21, 1402/01/01
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Expected recruitment end date
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2023-07-21, 1402/04/30
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Actual recruitment start date
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empty
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Actual recruitment end date
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empty
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Trial completion date
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empty
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Scientific title
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A comparative study of the effectiveness of oral phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
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Public title
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Comparative study of the effectiveness of oral phenytoin
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Purpose
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Diagnostic
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Inclusion/Exclusion criteria
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Inclusion criteria:
Patients with bipolar disorder in manic episode based on DSM-5 criteria
Patients should be in the age range of 18 to 40 years
To have the ability to perform and cooperate in psychological tests
Absence of pregnancy and the postpartum period
Not having severe medical illness, especially convulsions
Exclusion criteria:
History of drug sensitivity
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Age
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From 18 years old to 40 years old
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Gender
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Both
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Phase
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1-2
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Groups that have been masked
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No information
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Sample size
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Target sample size:
70
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Randomization (investigator's opinion)
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Randomized
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Randomization description
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70 patients are randomized in a simple way using a table of random numbers (to use the table of random numbers, first the framework of the statistical community is determined (70 people); respectively, we give them a code or serial number. Codes and numbers It should be equal to that assigned to the members of society; for example, in our research, we give two-digit codes to people, such as 01, 02, 03, ..., 11, 12, ....
To select sample people from the table, we randomly start from a point in the table in the row or column direction. We can choose the point by closing our eyes and placing a finger or the tip of a pen on the table. Moving in the direction of row or column does not differ and this is optional. But according to the type of code digits (one digit, two digit, three digit, etc.), we must choose the same number of digits in the direction of row or column. After this, we control the route numbers. Whether we like it or not, we will come across two types of numbers, one type of which is smaller than the number of the studied community and the other type is larger than the number of the community. We should pay attention to and choose only the smaller numbers. The selected number is actually the code of an individual from the community that is selected as a sample. This work should continue until the number of sample people can be chosen as small as possible. After the sample volume is complete, the sampling work ends.
The numbers will be placed in sealed envelopes, and when the participants enter, an envelope will be assigned to each of them, and they will be placed in one of the 2 intervention groups.
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Blinding (investigator's opinion)
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Not blinded
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Blinding description
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Placebo
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Not used
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Assignment
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Parallel
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Other design features
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Ethics committees
1
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Ethics committee
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Approval date
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2022-10-23, 1401/08/01
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Ethics committee reference number
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IR.MUMS.REC.1401.232
Health conditions studied
1
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Description of health condition studied
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bipolar
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ICD-10 code
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ICD-10 code description
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Primary outcomes
1
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Description
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Patient symptoms(behavioral stability and depression)
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Timepoint
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Before the intervention and 48 hours after the intervention
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Method of measurement
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Based on daily visits and YMRS, CGI tests
Intervention groups
1
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Description
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Intervention group:received oral phenytoin with an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose on a weekly basis until the dose of 600 mg.
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Category
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Treatment - Other
2
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Description
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Control group: Oral sodium valproate drug at a dose of 20 mg per kilogram of body weight will be taken daily for two weeks.
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Category
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Treatment - Other
1
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Sponsor
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Grant name
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Grant code / Reference number
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Is the source of funding the same sponsor organization/entity?
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Yes
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Title of funding source
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Mashhad University of Medical Sciences
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Proportion provided by this source
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100
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Public or private sector
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Public
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Domestic or foreign origin
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Domestic
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Category of foreign source of funding
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empty
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Country of origin
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Type of organization providing the funding
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Academic
Sharing plan
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Deidentified Individual Participant Data Set (IPD)
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Undecided - It is not yet known if there will be a plan to make this available
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Study Protocol
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Undecided - It is not yet known if there will be a plan to make this available
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Statistical Analysis Plan
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Undecided - It is not yet known if there will be a plan to make this available
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Informed Consent Form
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Undecided - It is not yet known if there will be a plan to make this available
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Clinical Study Report
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Undecided - It is not yet known if there will be a plan to make this available
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Analytic Code
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Undecided - It is not yet known if there will be a plan to make this available
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Data Dictionary
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Undecided - It is not yet known if there will be a plan to make this available