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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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12 December 2020 |
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Main ID: |
NCT03428503 |
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Date of registration:
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05/02/2018 |
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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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Comparison of Efficacy of Intravenous Paracetamol and Dexketoprofen for Acute Traumatic Musculoskeletal Pain
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Scientific title:
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Comparison of Efficacy of Intravenous Paracetamol and Dexketoprofen for Acute Traumatic Musculoskeletal Pain in the Emergency Department: A Double-Blinded, Randomized, Controlled Trial |
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Date of first enrolment:
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December 2015 |
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Target sample size:
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200 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03428503 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Factorial Assignment. Primary purpose: Treatment. Masking: Triple (Participant, Care Provider, Investigator).
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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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Atakan Yilmaz, 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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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients were eligible for inclusion if they were aged 18 years or older, 65 years or
younger
- Isolated traumatic musculoskeletal pain
- Patients who agree to work and receive the approval
- VAS (visual analog scale) score>5.
Exclusion Criteria:
- Patients with severe liver, kidney,pulmonary and cardiac heartfailure
- To be Pregnancy and breast-feeding
- Have received analgesics in the last 6hours
- Patients of childbearing age who are not using a birth control method.
- Patients with neurological deficits
- Patients with sciatica and back pain
- Patients with cardiac chest pain
- Patients with chronic pain
- Patients with pre-existing dexketoprofen and paracetamol-induced gastrointestinal
bleeding and perforation
- Patients with reflected pain
- Patients with neoplastic pain
- Patients with an allergy trait (paracetamol and dexketoprofen)
- Illiterates and patients with vision problems
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Musculoskeletal Pain
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Intervention(s)
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Drug: Dexketoprofen
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Drug: Paracetamol
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Primary Outcome(s)
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Decrement of the pain on VAS
[Time Frame: Baseline and 60 minutes]
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Secondary ID(s)
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2015HZL031
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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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