Musculoskeletal Injury Clinical Trial
Official title:
Synergistic Effect Of Parenteral Diclofenac And Paracetamol In The Pain Management Of Acute Limb Injuries
Verified date | February 2023 |
Source | Hamad Medical Corporation |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Acute limb injury is a common reason to visit an emergency department worldwide. Intense pain related to the injury is always a concern for an emergency physician and requires effective analgesia within the shortest possible time. Non-steroidal anti-inflammatory drugs (NSAIDs), opioids and paracetamol are the commonly used drugs in an emergency department. The choice of analgesia should be established by its efficacy, logistics involved and route of administration. There is good evidence about NSAIDs being the first line analgesia and paracetamol is reported to have the narcotic sparing effect, either alone or as an adjunctive treatment in different settings. The synergistic effect of paracetamol with diclofenac in acute limb injuries related pain management lacks good- quality evidence. Therefore investigators proposed a large, well designed, randomized double-blind trial to develop high-quality evidence. The study aims to assess the efficacy of paracetamol in addition to diclofenac, and compare the difference between oral and intravenous paracetamol administration in acute limb injuries in the emergency department.
Status | Completed |
Enrollment | 162 |
Est. completion date | February 21, 2023 |
Est. primary completion date | February 21, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Age 18 years upto 65 years - Vitals Stable - musculoskeletal limb injury - initial pain score of 5 or more on a NRS (numerical rating scale) Exclusion Criteria: - Patient received any pain medication prior to 8 hours - Allergies to either diclofenac or paracetamol - Contraindication to the study drugs - CVA - Bronchial asthma - GI bleeding - Renal impairment - Asthma - Pregnancy and nursing - Unstable traumatic patient |
Country | Name | City | State |
---|---|---|---|
Qatar | Hamad Medical Corporation | Doha |
Lead Sponsor | Collaborator |
---|---|
Hamad Medical Corporation |
Qatar,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To compare the difference in mean pain reduction amongst the three groups: numerical rating scale | Pain score on a numerical rating scale (NRS). The scale is a 11 point scale where 0 is no pain and 10 is the worst pain ever. | 30 minutes | |
Secondary | To compare the difference in proportion of patients achieving 50% or more pain relief amongst the three groups | Pain score on a numerical rating scale (NRS). The scale is a 11 point scale where 0 is no pain and 10 is the worst pain ever. | 30 minutes | |
Secondary | Requirement of rescue analgesia in each group of participants | Pain score on a numerical rating scale (NRS). The scale is a 11 point scale where 0 is no pain and 10 is the worst pain ever. | 30 minutes | |
Secondary | The adverse event rate in three groups | any adverse event recorded | 90 minutes | |
Secondary | Time to analgesia effect, to achieve 50% reduction, and to NRS <=2 | Pain score on a numerical rating scale (NRS). The scale is a 11 point scale where 0 is no pain and 10 is the worst pain ever. | 90 minutes |
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