Trials / Completed
CompletedNCT02714179
Preemptive and Preventive Use of Paracetamol for Pain Relief After Cesarean Section
A Double Blind Randomised Controlled Trial of Preemptive and Preventive Use of Paracetamol for Pain Relief After Cesarean Section
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 54 (actual)
- Sponsor
- Baskent University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
The investigators designed a prospective randomized study to investigate the efficacy of intravenous (IV) preemptive versus preventive paracetamol on postoperative pain scores, patient satisfaction, total morphine consumption and the incidence of morphine-related side effects in patients undergoing cesarean section.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Paracetamol was given intravenously in both group at different times |
Timeline
- Start date
- 2015-05-01
- Primary completion
- 2016-01-01
- Completion
- 2016-01-01
- First posted
- 2016-03-21
- Last updated
- 2016-03-21
Source: ClinicalTrials.gov record NCT02714179. Inclusion in this directory is not an endorsement.