Trials / Unknown
UnknownNCT02425254
Preemptive Paracetamol for Postoperative Pain
Preemptive Paracetamol for Postoperative Pain: a Randomised, Double-blind, Two Way Crossover Trial
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- University of Nottingham · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to test whether a dose of paracetamol given before surgical incision is more effective at reducing postoperative pain and analgesic consumption in cervical spine surgery versus a dose given at the end of surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Intravenous paracetamol | 1000mg intravenous solution for infusion |
| DRUG | Intravenous saline 0.9% | 0.9% sodium chloride in order to ensure double-blinding |
Timeline
- Start date
- 2016-01-01
- Primary completion
- 2017-06-01
- Completion
- 2018-07-01
- First posted
- 2015-04-23
- Last updated
- 2015-12-03
Source: ClinicalTrials.gov record NCT02425254. Inclusion in this directory is not an endorsement.