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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05327075
Other study ID # IRB 00012367-22-03-001
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 15, 2022
Est. completion date December 2022

Study information

Verified date July 2022
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

it is a cross-sectional study conducted in female patients attending outpatient clinc in our university hospital to assess their awareness regarding the symptoms of premenstrual dysphoric disorders.


Description:

this study will be conducted on females in the reproductive age attending the gynecological outpatient clinic to assess the prevalence of premenstrual dysphoric disorder(eeiPMDD) and their awareness regarding the symptoms of PMDD and the impact of these symptoms on their quality of life using questionnaire including ( knowledge , attitude and practice) of those Egyptian females.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date December 2022
Est. primary completion date September 2022
Accepts healthy volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: females in reproductive age history of regular menstruation Exclusion Criteria: history of any psychological disorders history of chemotherapy in last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaire
it is in the form of questionnaire and scoring tool

Locations

Country Name City State
Egypt Al Azhar University Hospital in Damietta Damietta

Sponsors (1)

Lead Sponsor Collaborator
Al-Azhar University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary questionnaire " awareness of participants regarding PMDD symptoms" knowledge , attitude and practice through the time of questionnaire during the study, an avarege 1 month
Secondary questionnaire "impact of the PMDD symptoms on the participants life" impact on their life questionnaire 3 months
See also
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