Trial reportBMC anesthesiology2025
Esketamine prevents carboprost-induced adverse reactions during cesarean section under combined spinal-epidural anesthesia: a double-blind, randomized trial.
Trial report in BMC anesthesiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Esketamine for postoperative sleep disturbance: clinical evidence, mechanisms, and future directions.Frontiers in psychiatry · 2025Review
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Authors and funding
7 authors.
Funding
Abstract
objectivesTo investigate adverse reactions to carboprost reduced by intravenous esketamine administered after childbirth via cesarean delivery with the patient under combined spinal-epidural anesthesia.
methodsThe study enrolled pregnant women aged 20-40 years, with American Society of Anesthesiologists (ASA) class II or III, and a gestational age of 37 weeks or more. These women had a scheduled cesarean section procedure with the administration of combined spinal-epidural anesthesia. Patients were randomized to receive esketamine 0.5 mg/kg (Group E) or volume-matched normal saline (Group C) immediately after fetal delivery, prior to carboprost administration (250 µg intramuscularly). The primary outcome was the incidence of vomiting during surgery. The secondary outcomes were the incidence of adverse reactions (nausea, chest rigidity, flushed face, tachycardia, cough, shivering), vital signs (HR, RR, MAP, SPO
resultsEighty-one pregnant women completed the study. The incidence of vomiting (22.5% vs. 56.1%, p < 0.001) and the incidence of nausea, chest rigidity, flushed face, and hypertension were significantly lower in group E than in group C (all p < 0.01), but the incidence of tachycardia was higher in group E (45% vs. 19.5%, p < 0.001). Furthermore, the patients' arterial partial pressure of oxygen was significantly higher in group E than in group C (91.90 ± 5.14 vs. 79.76 ± 3.96, p < 0.001). Postoperative pain at the incision site, as assessed by Visual Analogue Scale (VAS) score, was significantly reduced at 6 h in the Esketamine group compared to the control group. However, there was no significant difference in uterine contraction pain between the two groups at any time point.
conclusionFor women undergoing cesarean delivery under combined spinal-epidural anesthesia, intravenous esketamine administered after delivery of the fetus and prior to carboprost administration during cesarean section under combined spinal - epidural anesthesia was associated with a reduction in the incidence of carboprost - induced adverse reactions and a decrease in postoperative incision pain at 6 h. However, it did not significantly affect postoperative uterine contraction pain.
trial registrationChinese Clinical Trial Registry (Registration number# ChiCTR2100054985); Date of Registration: 30/12/2021.
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