Finding studies
Finding studies
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Lead
The University of Texas Health Science Center, Houston
Rationale for this clinical trial The goal of analgesia in pregnancy is to reduce pain while minimizing both maternal and fetal adverse effects. Current opioids used in pregnancy provide minimal pain relief and are associated with adverse effects. IV acetaminophen has been shown to significantly improve pain control following cesarean section and in the first stage of labor. Moreover, IV acetaminophen reduces the need and consumption of opioids following surgery. If IV acetaminophen can be as effective in controlling pain associated with maternal medical conditions and uterine contractions with labor, then the use of parenteral opioids in pregnant women and its exposure to the fetus could be reduced. This could provide new opportunities in the medical management of pain in pregnancy. Thus we propose a comparative effectiveness trial of IV acetaminophen compared to IV morphine. Hypothesis: We hypothesize that IV acetaminophen is as effective as IV morphine in reducing pain in pregnant women. In doing so, IV acetaminophen can reduce the amount of narcotics needed in women with pain. Objectives: To determine if IV acetaminophen can: 1. Decrease pain in pregnant women 2. Reduce the amount of opioid use in pregnant women who encounter pain 3. Reduce maternal and fetal adverse effects compared to opioids Study Design: For this comparative effective trial, we propose a randomized, controlled trial of IV acetaminophen vs. IV morphine in pregnant women. Prior studies have confirmed that IV acetaminophen is effective in controlling pain compared to placebo.\[14,20\] Thus, administering just a placebo for pain control is not justified at this time. We will include 3 different groups of pregnant populations who encounter pain for different reasons. Group 1: Pregnant women with uterine contractions, but not in labor Group 2: Pregnant women with uterine contractions in the first stage of labor Group 3: Pregnant women with a medical condition associated with pain.
Age
18–60
Sex
FEMALE
Healthy volunteers
Not accepted
