Postoperative Nausea and Vomiting Clinical Trial
Official title:
Effect of Right-stellate Ganglion Block in Preventing Postoperative Nausea and Vomiting in Gynecological Laparoscopic Patients
Postoperative nausea and vomiting is one of the common postoperative complications. Studies have reported that without any antiemetic prevention treatment, the overall incidence of PONV in surgical operations is up to 20-30%, and the incidence of PONV in high-risk operations such as gynecological laparoscopy is higher. Postoperative nausea and vomiting can lead to perioperative complications and seriously affect the prognosis of patients. Although various preventive and therapeutic measures have been adopted in clinic, the incidence of perioperative nausea and vomiting is still high. Therefore, it is of great clinical significance to explore more effective and feasible methods to prevent the occurrence of PONV. Stellate ganglion block has been proved to be widely used in clinic and can play a positive role in multiple organs and systems of the whole body. In clinical work, stellate ganglion block is more widely used in the treatment of various pain, autonomic nerve disorders and other diseases. However, there are few clinical studies on whether stellate ganglion block can be used as an effective and feasible means to prevent postoperative nausea and vomiting and the related mechanisms to prevent the possible occurrence of nausea and vomiting. Therefore, this project aims to explore the preventive effect of stellate ganglion block on postoperative nausea and vomiting in gynecological laparoscopic surgery patients, and to explore its possible mechanism.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | August 30, 2024 |
Est. primary completion date | May 30, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: 1. Age =18 years and = 70 years 2. American Society of Anesthesiologists(ASA) physical status classification I-Ill. 3. Voluntary participation and ability to understand and sign the informed consent form 4. Patients undergoing gynecological laparoscopic surgery elective general anesthesia Exclusion Criteria: 1. Patients with obesity(BMI>30kg/m2) 2. Contraindicated to stellate ganglion block 3. Patients who cannot cooperate with the study for any reason,or whom the investigator deems unsuitable for inclusion in this trial. |
Country | Name | City | State |
---|---|---|---|
China | The Second Affiliated Hospital of Chongqing Medical University | Chongqing | Chongqing |
Lead Sponsor | Collaborator |
---|---|
The Second Affiliated Hospital of Chongqing Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The incidence of postoperative nausea and vomiting | Postoperative nausea and vomiting is evaluated by follow-up | From end of surgery to 24 hours after surgery | |
Secondary | Incidence of nausea and vomiting during preemptive analgesia | Postoperative nausea and vomiting is evaluated by investigator's follow-up | From 0-10 min after preemptive analgesia | |
Secondary | Intensity of nausea and vomiting during preemptive analgesia | ntensity of nausea and vomiting (the scale is Rhodes index of nausea and vomiting)is evaluated by numerical rating scale (0-10), which higher socre represents more severe the nausea and vomiting | From 0-10 min after preemptive analgesia | |
Secondary | Intensity of nausea and vomiting during hospitalization | Intensity of nausea and vomiting is evaluated by numeric rating scale (0-10), which higher socre represents more uncomfortable | From end of surgery to 24 hours after surgery | |
Secondary | Hemodynamic parameters | Mean arterial pressure in mmHg,heart rate in bpm,oxygen saturation(%) | Before stellate ganglion block and From 0-30 min after Satellite Ganglion Blocks | |
Secondary | Postoperative pain intensity | Postoperative pain intensity is assessed by numeric rating scale (0-10), which higher socre represents more uncomfortable | From end of surgery to 24 hours after surgery | |
Secondary | Recovery of gastrointestinal function | Gastrointestinal function is is assessed by the evacuation time | From end of surgery to 24 hours after surgery | |
Secondary | Sleep quality | Sleep quality is is assessed by numeric rating scale (0-10), which higher socre represents better sleep quality | From end of surgery to 1 day after surgery | |
Secondary | Satisfaction score and postoperative analgesia satisfaction score | Satisfaction score and postoperative analgesia satisfaction score is assessed by numeric rating scale (0-10), which higher socre represents more comfortable | From end of surgery to hospital discharge with about 5 days |
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