Prevalence of Menstrual Cycle Related Pain Complains in Adolescents and Young Adults
NCT ID: NCT00590811
Last Updated: 2010-09-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
200 participants
OBSERVATIONAL
2008-01-31
2010-02-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Adolescent Dysmenorrhoea as a Risk Factor for Chronic Pain: Clinical Cohort Study
NCT06353789
Female Chronic Pelvic Pain
NCT01255345
Chronic Pelvic Pain in Endometriosis
NCT05863663
Chronic Pain Risk Associated With Menstrual Period Pain
NCT02214550
Pelvic Pain in Women With Endometriosis
NCT00073801
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Adolescents
* start of menstruation
* characteristics of menstrual cycle
* pain related to menstrual cycle (questions based on well-known pain-complaints related to the presence of endometriosis)
* analgetics
* influence on school carrier
* influence on social life
Young adults
* idem as for adolescents
* influence of pain on an eventual sexual relationship
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
adolescents
3rd year high school girls (14-16 years old)
No interventions assigned to this group
young adults
1st year university young females (18 - 20 years old)
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 1st year university young females
Exclusion Criteria
12 Years
25 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Gasthuisberg
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
University Hospital Leuven, Leuven, Belgium
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Christel LC Meuleman, MD
Role: PRINCIPAL_INVESTIGATOR
Universitaire Ziekenhuizen KU Leuven
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
MPTC
Leuven, , Belgium
VCLB
Leuven, , Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
EC - 14/11/2007
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.