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Abortion Complication clinical trials

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NCT ID: NCT06435949 Not yet recruiting - Clinical trials for Abortion Complication

Effect of Oxycodone on Anxiety State in Painless Abortion

Start date: July 1, 2024
Phase: Early Phase 1
Study type: Interventional

In this study, 300 patients who underwent painless abortion in Ruijin Hospital and sub-central hospitals were selected through a multi-center randomized controlled study, and 300 patients who underwent painless abortion in Ruijin Hospital and each sub-center hospital were divided into intravenous anesthesia with propofol with fentanyl (group F) and propofol with oxycodone (group O) by stratified group randomization method 1:1. The difference between the postoperative anxiety scores and depression scores of the two groups was observed, and the postoperative anxiety, depression and numerical pain scores were recorded. Finally, the relevant data were statistically analyzed and conclusions were drawn.