Musculo-scrawny Manifestation Associated With the Endometriosis
Sponsor
Groupe Hospitalier Paris Saint Joseph (Other)
Overall Status
Completed
CT.gov ID
NCT03305120
Collaborator
(none)
41
1
3.5
11.8
Study Details
Study Description
Brief Summary
The endometriosis is defined by the presence of endometriosic tissue outside of the womb and the prevalence is estimated to be 10% of women.Here is a project aimed to compare musculo-scrawny pains between patients with endometriosis and whose don't suffer of this pathology;
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
41 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Musculo-scrawny Manifestation Associated With the Endometriosis
Actual Study Start Date
:
Sep 16, 2016
Actual Primary Completion Date
:
Oct 16, 2016
Actual Study Completion Date
:
Dec 31, 2016
Outcome Measures
Primary Outcome Measures
- VAS of musculo-scrawny pain [Day 1]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
age between 18 and 45
-
consulting in Service of gynecology
-
First trimester of pregnancy or for pap smears
Exclusion Criteria:
-
endometriosis diagnostic already done
-
rhumalogic disease known
-
age < 18 and > 50
-
menopause
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Groupe Hospitalier Paris Saint Joseph | Paris | Ile-de-France | France | 75014 |
Sponsors and Collaborators
- Groupe Hospitalier Paris Saint Joseph
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Groupe Hospitalier Paris Saint Joseph
ClinicalTrials.gov Identifier:
NCT03305120
Other Study ID Numbers:
- ENDOMETRI-OS
First Posted:
Oct 9, 2017
Last Update Posted:
Oct 9, 2017
Last Verified:
Oct 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: