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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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9 March 2015 |
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Main ID: |
NCT02373514 |
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Date of registration:
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23/02/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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IV Paracetamol Versus IV Dexketoprofen in Dysmenorrhea
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Scientific title:
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Intravenous Paracetamol Versus Intravenous Dexketoprofen in Patients Presented With Dysmenorrhea in Emergency Department |
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Date of first enrolment:
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January 2015 |
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Target sample size:
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100 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02373514 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 4
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Countries of recruitment
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Turkey
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Contacts
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Name:
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Mustafa Serinken, MD |
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Address:
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Telephone:
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0090 505 2991497 |
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Email:
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aserinken@hotmail.com |
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Affiliation:
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Name:
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Mustafa Serinken, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Pamukkale University |
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Name:
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Cenker Eken, Medical Doctor |
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Address:
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Telephone:
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0090 532 1593948 |
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Email:
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cenkereken@akdeniz.edu.tr |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients with dysmenorrhea
- Patients over 18 years old
Exclusion Criteria:
- denied to give inform consent
- Renal or liver failure
- Allergy to the study drugs
- Receiving pain killer within the last 6 hours.
- Physical examination findings consistent with peritoneal irritation
- Pregnancy or patients with lactation
- Drug addiction
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Dysmenorrhea
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Intervention(s)
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Drug: Paracetamol
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Drug: Dexketoprofen
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Primary Outcome(s)
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Visual Analogue Scale
[Time Frame: 30 minutes]
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Visual Analogue Scale
[Time Frame: 15 minutes]
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Secondary Outcome(s)
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Rescue drug need
[Time Frame: 30 minutes]
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Adverse effects
[Time Frame: 30 minutes]
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Secondary ID(s)
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57051259-020/70177
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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