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The effectiveness of calcium with magnesium and only calcium on the pain severity and resting lenght with primary dysmenorrhea

The effectiveness of calcium with magnesium and only calcium on the pain severity and resting time with primary dysmenorrhea: a triple-blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202013706N10
Enrollment
60
Registered
2012-05-13
Start date
2012-05-14
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

primary dysmenorrhea. primary dysmenorrhea

Interventions

Intervention 1: Intervention 1: Taking Capsules containing 600 mg Calcium once a day from day 15 of menstural cycle to reliefing dysmenorrhea in the following cycle. Intervention 2: Intervention 2: Ta
Treatment - Drugs
Intervention 1: Taking Capsules containing 600 mg Calcium once a day from day 15 of menstural cycle to reliefing dysmenorrhea in the following cycle
Intervention 2: Taking Capsules containing 600 mg Calcium and 300 mg magnesium once a day from day 15 of menstural cycle to reliefing dysmenorrhea in the following cycle
Control group: Taking Placebo Capsules once a day from day 15 of menstural cycle to reliefing dysmenorrhea in the following cycle

Sponsors

Tabriz University of Medical Sciences, Aras branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 34 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Single students aged 18-34 years residing in Aras dormitory, having primary dysmenorrhea, regular and painful menstruation in previous 1 year with pain score equal or more than 5 according to visual analogue scale (medium to severe dysmenorrhea); consent to participate the study Exclusion criteria: Known serious diseases like epilepsy, severe digestive disorders, cardiovascular or renal diseases, pelvic inflammatory diseases; consumption of oral contraceptive pills in previous 6 months or desire to take them during study; allergy to NSAIDs.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mean severity of menstrual pain. Timepoint: for 2 months after intervention, 1 day before starting mensturation tol 3 days after it, measured once every 6 hours. Method of measurement: Visual Analogue Scale.;Resting length due to dysmenorhea. Timepoint: for 2 months after intervention. Method of measurement: daily recording of resting length by the participants on a form.

Secondary

MeasureTime frame
Symptom Severity during Mensturation. Timepoint: during 2 months after intervention. Method of measurement: Symptom Severity Scale.;Need to take additional pain relief drug for dysmenorrhea. Timepoint: for two months after starting intervention. Method of measurement: No of Mephenamic Capules used.;Volume of menstural bleeding. Timepoint: for two months after starting intervention. Method of measurement: Higham table.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSalime Nezamivand-Chegini

Tabriz University of Medical Sciences, Aras Unit

Nezamivandsalime@yahoo.com00

Outcome results

None listed

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