The purpose of this study is to determine whether intravenous paracetamol is effective in treating labor pain.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
King Abdulaziz Medical City
Riyadh, Central, Saudi Arabia
Visual analogue scale (VAS) score for pain
Patients who give written informed consent to participate will be entered into the study. Their VAS score will be determined every hour from the time of randomization until delivery of the baby. This time will vary from one patient to another depending on the duration of labor.
Time frame: Up to 24 hours
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