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NCT04808843Completed

A Study to Learn More About How Safe Dienogest is and How Well it Works Under Real World Conditions in Indian Women With Endometriosis

Phase IV Study to Assess the Safety and Effectiveness of Dienogest (Visanne®) Amongst Indian Women With Endometriosis, in Real-world Clinical Practice: the VISAGE Study

Source: ClinicalTrials.gov · Last updated 22 Jan 2025

Brief summary (registry, in English)

Endometriosis is a condition that affects women, usually during their reproductive years. In women with endometriosis, the tissue that normally covers the inside of the womb grows outside the womb. This can cause pain during their periods or during sex, and constant pain in the pelvis. Endometriosis can decrease a woman's quality of life. It also requires long-term treatment to control the symptoms. The study drug, dienogest, has already been approved as a treatment for endometriosis associated pelvic pain. Sometimes, researchers continue studying a treatment after it has been approved to learn more about its safety. In this study, the researchers want to learn more about any medical problems the patients have while taking dienogest. To answer this question, the researchers will collect the medical problems the patients have after taking dienogest and that may or may not be related to dienogest. These medical problems are also known as adverse events. They will also collect information about the endometriosis associated pelvic pain. The pain measured with a standard rating scale called EAPP (endometriosis-associated pelvic pain) before treatment start and after 6 months of treatment will be compared. The trial will include women with endometriosis associated pelvic pain whose doctors have decided to start treating them with dienogest. It will include about 160 women in India who are at least 18 years old. All of the patients will take dienogest based on their doctor's instructions. They will then visit their study site 3 times over 6 months. At these visits, their doctors will ask them questions about how they are feeling and what medications they are taking. The doctors will do tests to measure the pain caused by the patients' endometriosis and any other symptoms. The doctors will also do physical examinations and check the patients' overall health.

Status (registry)
Completed
Study type
Observational
Enrollment
160 (actual)
First submitted
18 Mar 2021
Start date
13 May 2022
Primary completion date
5 Feb 2024
Lead sponsor
Bayer
NCT number
NCT04808843

What you commit to

  • Study type: Observational
  • Participants enrolled: 160
  • From 13 May 2022 to the primary completion date, 5 Feb 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Participation in an investigational program with interventions outside of routine clinical practice
  • Contra-indications according to the local summary of product characteristics (SPC)

Who the study is looking for

  • Female patients in India at least 18 years of age
  • Clinical or surgical diagnosis of endometriosis: Clinical diagnosis by suggestive symptoms and positive finding in imaging study (Chocolate cyst)
  • Patients diagnosed with endometriosis associated pelvic pain who have not been previously treated with Dienogest
  • Decision to initiate treatment with Dienogest was made as per investigator's routine treatment practice
  • Signed informed consent

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Many locations
Coordinator of this site? Confirm its status
Multiple LocationsIndiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.