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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02369133
Study type Interventional
Source Baskent University
Contact
Status Completed
Phase Phase 4
Start date November 2013
Completion date November 2014

See also
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