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The Effect of Vitamin B1 on the menstruation’s complications

The Effect of Vitamin B1 on the menstruation’s complications Living in a dormitory students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017070710451N2
Enrollment
98
Registered
2017-07-14
Start date
2016-10-08
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

Pain and other conditions associated with female genital organs and menstrual cycle Excessive, frequent and irregular menstruation. N94.4 Primary dysmenorrhoeaN92.0 Excessive and frequent menstruation with regular cycle

Interventions

Sponsors

Islamic Azad University,Borujerd Branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 26 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: unmarried; age18-26; being literate; having regular menstruation period between 26-30 days; Pain a few hours before or at the same time occur with menstrual bleeding; Menstrual pain can take 3 days or less; menstruations bleeding duration more than7 days;the number of used sanitary napkins more than 14 numbers; Is not known medical illness; Is not special diet such as weight loss diet, obesity, vegetarian and water treatment; Do not use Tobacco or alcohol; Do not regular exercise.Exclusion criteria: The use of oral contraceptives or other steroid hormones; Existing of any kind of genital system diseases ;Background for kidney stone or any problems; any kind of diagnosed physical and psychological diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menstrual blood loss. Timepoint: Within 5 months with intervals of 1 month before intervention(at first) , and within 3 months after intervention and 1 month after finishing the intervention. Method of measurement: Higham chart.;Pain intensity. Timepoint: Within 5 months with intervals of 1 month before intervention(at first) , and within 3 months after intervention and 1 month after finishing the intervention. Method of measurement: Multidimensional questionnaires grading scales.;Pain duration. Timepoint: Within 5 months with intervals of 1 month before intervention(at first) , and within 3 months after intervention and 1 month after finishing the intervention. Method of measurement: based on hours.

Secondary

MeasureTime frame
Spotting. Timepoint: Within 5 months with intervals of 1 month before intervention(at first) , and within 3 months after intervention and 1 month after finishing the intervention. Method of measurement: Higham chart.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactziba latifiyan

Islamic Azad University,Borujerd Branch

zb.latifiyan@yahoo.com+98 66 4251 3042

Outcome results

None listed

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