Trial Condition(s):
Menorrhagia
A Swedish questionnaire study to investigate the perception of menstrual bleedings
Bayer Identifier:
16384
ClinicalTrials.gov Identifier:
EudraCT Number:
Not Available
EU CT Number:
Not Available
Study Completed
Trial Purpose
This field based, questionnaire study will document observational data on womens perception of menstrual bleeding in a cross-section of women in Sweden. Each subject will complete the questionnaire at one occasion.
Inclusion Criteria
- All women 40-45 years available in the web-panel of SIFO - Completion of the web-based questionnaire
Exclusion Criteria
- None
Trial Summary
Enrollment Goal
1547
Trial Dates
Phase
N/A
Could I receive a placebo?
No
Products
No Drug
Accepts Healthy Volunteers
Yes
Where to Participate
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Locations
| Locations | |
|---|---|
Locations Investigative Site Many Locations, Sweden | Contact Us: E-mail: [email protected] Phone: Not Available |
Trial Design
A Swedish cross-sectional study with questionnaire to investigate perception of menstrual bleeding
Trial Type:
Observational
Intervention Type:
Behavioral
Trial Purpose:
N/A
Allocation:
N/A
Blinding:
N/A
Assignment:
N/A
Trial Arms:
1
Primary Outcome
- Prevalence of subjectively experienced heavy menstrual bleeding assessed by questionnaireTimeframe: Once at baseline
Secondary Outcome
- Social consequences of heavy menstrual bleedings assessed by questionnaireTimeframe: Once at baseline
- Costs; e.g. pads, absence from work, loss of income assessed by questionnaireTimeframe: Once at baseline
- The treatments given for heavy menstrual bleedings, as surgery or medication assessed by questionnaireTimeframe: Once at baseline
Additional Information
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