Pain
Conditions
Brief summary
Allow gynecologists to gain experience with arcoxia for treatment of dysmenorrhea.
Interventions
Sponsors
Organon and Co
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 25 Years
Healthy volunteers
No
Inclusion criteria
* Healthy women older than 18 years old and younger than 25 years old * Voluntary agreement to participate in the study and signature of informed consent * Women with clinical diagnosis of dysmenorrhea
Exclusion criteria
* Diagnosis of secondary dysmenorrhea due to: endometriosis, adenomyosis, malformations of Muller's conducts, uterine fibromyomas, ovarian cystic, pelvic varicocoele, inflammatory pelvic disease, adherences, intrauterine devices, cervical channel stenosis, etc. * Patients with diagnosis of acute inflammatory abdomen * Patients with diagnosis of congestive heart disease, stroke (1 year), unstable angina, and history of myocardial infarction * Women auto prescribing rescue medication for dysmenorrheal pain during the study * Women with a diagnosis of mild dysmenorrhea
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Perception of menstrual pain, through the analog verbal scale during three days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life measures during three days. | — |
Outcome results
None listed