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NCT05414825: DEMETER

Dysmenorrhea Exploration in Teenagers, Their Parents and Caregivers

Completed Last updated 4 November 2022
What this trial tests

trial testing focus group interview in Dysmenorrhea in 27 participants. Completed in 13 September 2022.

Timeline
29 August 2022
Primary endpoint
13 September 2022
13 September 2022

Quick facts

Lead sponsorUniversity Hospital, Toulouse
StatusCompleted
Study typeOBSERVATIONAL
Enrollment27
Start date29 August 2022
Primary completion13 September 2022
Estimated completion13 September 2022
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Toulouse

Who can join

Adults 11 to 100, any sex, with Dysmenorrhea. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Teenagers experimenting severe dysmenorrhea also face age-specific challenges, particularly impacting their self-confidence, self-esteem, and relations. On one hand, the study team will conduct focus group interviews to better understand the experience of teenagers and their parents consulting pediatric services for severe dysmenorrhea. On the other hand, they will conduct focus group interviews with caregivers from services that usually encounter such patients (gastrologic, gynecologic and pain services). This, allowing to later propose specific tools and healthcare organization to evaluate and accompany teenagers suffering from severe dysmenorrhea.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Dysmenorrhea

Currently open trials in the same condition.

Other University Hospital, Toulouse trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05414825.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing