Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05156385

Sexual Dysfunction in Hypertensive Women

Led by University Hospital, Toulouse · Updated on 2024-10-23

348

Participants Needed

1

Research Sites

210 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Several studies describe the existence of an association between sexual dysfunction and high blood pressure (hypertension), most often characterized by a decrease in the number of orgasms and the existence of dyspareunia. Hypertension is a contributing factor, and nonadherence to medication could amplify it. There are several ways to assess adherence to treatment: the use of declarative questionnaires, a method not without criticism because it is subject to the subjectivity of the declaration by the patient; and drug dosages, a standard technique, although insufficiently disseminated due to the high cost and greater weight of the survey protocols. Drug non-compliance is multifactorial. In addition, it has been shown that having undesirable drug effects and / or being afraid of developing them is one of the major causes of non-compliance with antihypertensive treatments. The investigators hypothesize that DS is significantly more common among hypertensive women treated with non-observers compared to hypertensive women treated with observers. The main objective is to compare the prevalence of sexual dysfunction between a group of hypertensive women treated as observers and a group of hypertensive women treated as non-observers.

CONDITIONS

Official Title

Sexual Dysfunction in Hypertensive Women

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women over 18 years old
  • Hospitalized or seen in consultation for hypertension management in participating nephrology, cardiology, or hypertension departments
  • Confirmed hypertension treated with at least one of the specified dosable antihypertensive agents
  • Signed informed consent form
  • Beneficiary or affiliated with French Social Insurance
Not Eligible

You will not qualify if you...

  • Patients who have had bariatric surgery
  • Patients under guardianship, trusteeship, or legal protection
  • Patients diagnosed and treated for psychosis or depression
  • Pregnant or nursing women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

LAZARO Delphine

Toulouse, CHU de Toulouse, France, 31059

Actively Recruiting

Loading map...

Research Team

D

Delphine LAZARO-VERGE

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here