Comparison of Dexketoprofen, Paracetamol and Ibuprofen in the Treatment of Primary Dysmenorrhea

Launched by PAMUKKALE UNIVERSITY · Oct 4, 2018

Keywords

ClinConnect Summary

Our research will be carried out in Pamukkale University Faculty of Medicine Department of Emergency Medicine in 12 months period. There will be a research assistant and / or a faculty member who will control the research for 24 hours in our emergency department with approximately 110000 adult patients / year.

Study criteria: Female patients with primary dysmenorrhea (abdomino-pelvic pain) in the 18-45 age range. The onset of symptoms should usually be a few hours - 1 day before the onset of visible vaginal bleeding. Possible systemic symptoms such as nausea, vomiting, diarrhea, headache, ...

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • Female patients with primary dysmenorrhea (abdomino-pelvic pain) between the ages of 18-45.
• • The onset of symptoms should usually be a few hours - 1 day before the onset of visible vaginal bleeding.
• • Possible systemic symptoms such as nausea, vomiting, diarrhea, headache, fatigue, irritability, and dizziness are also questioned and recorded in the data form.
• • Patients with visual analogue scale score\> 5 and those who need or need nonsteroidal anti-inflammatory treatment.
• Exclusion Criteria:
• • Severe liver, kidney and heart failure; asthma, nasal polyp, angioedema and urticaria against aspirin or other nonsteroidal antiinflammatory drugs;
• • Active peptic ulcer, bleeding or perforation; to have a history of upper gastrointestinal disease;
• • Patients with phenylketonuria;
• • During pregnancy and lactation;
• • Have asthma;
• • Have taken analgesics in the last 4 hours;
• • The age of pregnancy and not using birth control method; digoxin, lithium, furosemide and other diuretics, acetylsalicylic acid and coumarin group using anticoagulants and physical examination of the suspicion of acute abdomen and signs of peritoneal irritation.