Trials / Completed
CompletedNCT02369133
Preemptive Analgesia With Intravenous Paracetamol for Post-cesarean Section Pain Control
Preemptive Analgesia With Intravenous Paracetamol for Post-cesarean Section Pain Control : A Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Baskent University · Academic / Other
- Sex
- Female
- Age
- 20 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
The investigators designed a prospective randomized study to investigate the efficacy of intravenous (IV) preemptive paracetamol on postoperative pain scores, patient satisfaction, total morfin consumption and the incidence of morfin-related side effects in patients undergoing cesarean section.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | paracetamol | Drugs were given intravenously by a nurse unaware of the study 15 min before surgery. Patients in group P (n = 30) received 1 g iv paracetamol, patients in group S (n = 30) received 100 ml iv %0.9 NaCl |
| DRUG | Placebo |
Timeline
- Start date
- 2013-11-01
- Primary completion
- 2014-02-01
- Completion
- 2014-11-01
- First posted
- 2015-02-23
- Last updated
- 2015-02-23
Source: ClinicalTrials.gov record NCT02369133. Inclusion in this directory is not an endorsement.