Viewing Study NCT06487754



Ignite Creation Date: 2024-07-17 @ 11:05 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06487754
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-05
First Post: 2024-06-19

Brief Title: New-onset Chronic Pelvic Pain in Transgender People Using Testosterone Therapy an Exploratory Qualitative Study
Sponsor: University Hospital Grenoble
Organization: University Hospital Grenoble

Study Overview

Official Title: New-onset Chronic Pelvic Pain in Transgender People Using Testosterone Therapy an Exploratory Qualitative Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This descriptive qualitative study aim to describe the characteristics of pelvic pain in transgender trans individuals using testosterone therapy and the impact on their quality of life This study also aim to understand the levers and obstacles to consulting a health care professional
Detailed Description: This study ai to accurately describe the chronic pelvic plan CPP from which transmasculine people can suffer as well as their impact on quality of life and to understand what are the obstacles and levers to the implementation of adapted care

Method It is an observational single-center qualitative study 10 to 15 trans individuals using testosterone therapy and having pelvic pain for at least 6 months and that had appeared or changed since taking testosterone will undergo a semi-structured interview They will be recruited through community care associations mailing lists and flyers

Results This is a qualitative study aimed at accurately describing the symptoms of pelvic pain experienced by trans people thus we will do a qualitative analysis QCAMAPS will be used for the coding step

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None