Nova Gradiska General Hospital
Strossmayerova 17, Croatia
NCT Number: NCT00517556
The primary hypothesis is that continuous administration of an OCP (CCOCP regimen) will result in more pain relief than a traditional 21/7 administration in primary dysmenorrhea (PD) patients.
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Notify Me18 year–35 year
Female
Interventional
Phase 1 / Phase 2
Strossmayerova 17, Croatia
It is well established that excess prostaglandin production in primary dysmenorrhea (PD) leads to ischemia of the uterine muscle, which consequently causes pelvic pain. A large number of drugs have been studied for pain relief in dysmenorrhea patients with non-steroid anti-inflammatory drugs (NSAIDs) being the most effective with the overall success rate of more than 75%. Oral contraceptive pills (OCP) are also an established treatment for PD with the success rate of 70%. Lately, OCP's have been used continuously in patients with endometriosis and had better pain control than traditional administration of OCP.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
(CCOCP) continuous treatment with Monophasic oral gestodene/ethinyl estradiol
Other names: Oral contraceptives
(traditional OCP) (21 active days/7 inactive days) treatment regimen
Other names: Oral contraceptives
Time frame: Baseline and 6 months
Change in subjective perception of pain, as measured by the VAS. Subjects completed the VAS at baseline and 6 months. The VAS ranges from 0 (no pain) to 100 (worst pain). Therefore, a negative change in VAS indicates improvement in pain and a positive change in VAS indicates worsening of pain.
Milton S. Hershey Medical Center
Other
Continuous Administration of a Monophasic Oral Contraceptive in the Treatment of Primary Dysmenorrhea
Acronym: Dysmenorrhea
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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