- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05072756
Opinion of Brazilian Gynecologists on Hormone Therapy for Menopause and Prescriptive Habits
Opinion of Brazilian Gynecologists on Hormone Therapy for Menopause and Prescriptive
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
There are few Brazilian population studies on the opinion of Brazilian gynecologists about the hormonal therapy of menopause in climacteric women, their prescriptive habits and their views on the availability of treatments offered, demanding better evaluation and justifying efforts to analyze the perception of professionals in this area in our country.
Methods: To assess gynecologists across the country, through structured online questionnaires, with questions aimed at knowing their opinions and prescriptive habits about menopause hormone therapy. Research participants will complete the questionnaires in digital format online. Doctors will be invited to participate by e-mail messages and by social media.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
SP
-
São Bernardo do Campo, SP, Brazil, 09760-280
- Centro de Atenção Integral à Saúde da Mulher
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Brazilian licensed gynecologist doctors
Exclusion Criteria:
- Retired doctors
- Health professionals other than medicine doctor
- Medical specialties other than Gynecology
- Medical employees of the pharmaceutical industry
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Gynecologists
Brazilian gynecologists who agreed to participate and answered the questionnaire
|
The participants have to answer a questionnaire addressing their opinion on menopausal hormone replacement therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prescription preference
Time Frame: At Day 1
|
Answer to the questionnaire addressing gynecologists' prescription habit for menopausal women
|
At Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Knowledge of window of opportunity for hormone replacement therapy
Time Frame: At Day 1
|
This is to see which proportion of gynecologists know the principle of window of opportunity for menopausal hormone replacement therapy
|
At Day 1
|
Knowledge of indications and contraindications of hormone replacement therapy
Time Frame: At Day 1
|
This is to see which proportion of gynecologists know the indications and contraindicationsv of menopausal hormone replacement therapy
|
At Day 1
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Taylor HS, Kagan R, Altomare CJ, Cort S, Bushmakin AG, Abraham L. Knowledge of clinical trials regarding hormone therapy and likelihood of prescribing hormone therapy. Menopause. 2017 Jan;24(1):27-34. doi: 10.1097/GME.0000000000000711.
- Buhling KJ, von Studnitz FS, Jantke A, Eulenburg C, Mueck AO. Use of hormone therapy by female gynecologists and female partners of male gynecologists in Germany 8 years after the Women's Health Initiative study: results of a survey. Menopause. 2012 Oct;19(10):1088-91. doi: 10.1097/gme.0b013e318250bfda.
- Yeganeh L, Boyle J, Teede H, Vincent A. Knowledge and attitudes of health professionals regarding menopausal hormone therapies. Climacteric. 2017 Aug;20(4):348-355. doi: 10.1080/13697137.2017.1304906. Epub 2017 Apr 5.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 40147120.8.0000.0082
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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