Many Locations, Sweden
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.
Looking for future studies?
Notify MeKey information
Conditions
Age range
40 year–45 year
Sex eligibility
Female
Study type
Observational
Primary location
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
BehavioralNo drug intervention. The intervention is a questionnaire with quality of life and perception of menstrual bleedings. All subjects will complete both questionnaires.
Primary outcomes
-
Prevalence of subjectively experienced heavy menstrual bleeding assessed by questionnaire
Time frame: Once at baseline
Secondary outcomes
-
Social consequences of heavy menstrual bleedings assessed by questionnaire
Time frame: Once at baseline
-
Costs; e.g. pads, absence from work, loss of income assessed by questionnaire
Time frame: Once at baseline
-
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.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Treatment of Non-Gestational Acute Uterine Bleeding: A Randomized Trial
NCT00350480
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
Los Angeles, California, United States
View Trial DetailsA Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment of Uterine Fibroids
NCT00160381
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
View Trial DetailsSafety of Treatment of Uterine Fibroids With Asoprisnil
NCT00156208
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
View Trial DetailsStudy to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids
NCT00156195
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
View Trial Details