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Completed

NCT Number: NCT01643304

A Swedish Questionnaire Study to Investigate the Perception of Menstrual Bleedings

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.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All women 40-45 years available in the web-panel of SIFO
  • Completion of the web-based questionnaire

Exclusion criteria

  • None

Treatment and study plan

No Drug

Behavioral

No drug intervention. The intervention is a questionnaire with quality of life and perception of menstrual bleedings. All subjects will complete both questionnaires.

Primary outcomes

  1. Prevalence of subjectively experienced heavy menstrual bleeding assessed by questionnaire

    Time frame: Once at baseline

Secondary outcomes

  1. Social consequences of heavy menstrual bleedings assessed by questionnaire

    Time frame: Once at baseline

  2. Costs; e.g. pads, absence from work, loss of income assessed by questionnaire

    Time frame: Once at baseline

  3. The treatments given for heavy menstrual bleedings, as surgery or medication assessed by questionnaire

    Time frame: Once at baseline

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

A Swedish Cross-sectional Study With Questionnaire to Investigate Perception of Menstrual Bleeding

Important dates

Study start
2012
Study completion
2012
First posted
Jul 18, 2012
Registry last updated
Nov 21, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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