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The effects of zinc compounds in the treatment of menstrual pai

Phase 2
Conditions
Primary dysmenorrhoea
Primary Dysmenorrhea.
Registration Number
IRCT201106186827N1
Lead Sponsor
Mother and Child Care Research Center, Vice Chancellor for Research and Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
64
Inclusion Criteria

Being volunteer to participate in the research; Having primary dysmenorrhea at least during three previous cycles which is approved by the researchers in the consultation; Having regular menstrual cycles between 21 days up to 35 days Having physical and mental health; Lack of using zinc as a dietary supplement during the last three months; Lack of sensitivity to zinc compounds

Exclusion criteria:
Changing Participant's mind for any reason and at any time ; Failure to attend counseling sessions; Failure to meet the guidelines defined in the study for any reason and at any time
Exclusion criteria:
Changing Participant's mind for any reason and at any time ; Failure to attend counseling sessions; Failure to meet the guidelines defined in the study for any reason and at any time

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of Dysmenorrhea. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Self-expressed Questionnaire.;Intensity of Dysmenorrhea. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: VAS.;Nausea and vomiting. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Nausea Scale.
Secondary Outcome Measures
NameTimeMethod
Duration of using conventional Medical treatments. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Self-expressed Questionnaire.;Amount of using conventional Medical treatments. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Self-expressed Questionnaire.;Duration of using conventional Non-medical treatments. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Self-expressed Questionnaire.;Amount of using conventional Non-medical treatments. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Self-expressed Questionnaire.;Failure to perform formal daily activities. Timepoint: Pre and Post interventional phase (two menstrual cycle). Method of measurement: Self-expressed Questionnaire.
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