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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06426186
Other study ID # PONV-Gynecological surgery
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 8, 2023
Est. completion date August 30, 2024

Study information

Verified date May 2023
Source The Second Affiliated Hospital of Chongqing Medical University
Contact ling Dan, BD
Phone 13983072922
Email 302069@hospital.cqmu.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Postoperative nausea and vomiting is one of the most common postoperative complications second only to postoperative pain. 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 patients such as gynecologic laparoscopy is higher. The pathogenesis of postoperative nausea and vomiting is very complex, including central, peripheral receptors and multiple nerve pathways. When peripheral receptors are stimulated, the signal passes through the afferent nerve to the vomiting center, causing nausea and vomiting. The emetic chemical receptors are rich in many receptors, which can directly feel various toxins, metabolites or drugs in the blood and cerebrospinal fluid, project signals to the nerve center and then spread to the cerebral cortex, causing nausea and vertigo, or transmit signals along the vagus nerve, glossopharyngeal nerve, spinal nerve, etc. to the digestive tract, diaphragm and abdominal wall muscles, resulting in the opening of the sphincter in the upper esophagus and strong contraction of the diaphragm. Abdominal muscles contract, so that the stomach pressure increases, stomach contents through the digestive tract is expelled from the body, vomiting. There are many factors affecting postoperative nausea and vomiting in gynecological laparoscopic surgery, including patient factors, anesthetic factors and surgical factors. Firstly, gender as an independent risk factor for postoperative nausea and vomiting is widely recognized by researchers, and a large number of studies have confirmed that the incidence of postoperative nausea and vomiting is higher in females, and the possible mechanism is caused by different hormone levels. Secondly, some studies believe that the type of surgery is also a risk factor for postoperative nausea and vomiting, but there is some controversy. In general, laparoscopic surgery patients have a higher incidence of postoperative nausea and vomiting. Finally, the mode of anesthesia and anesthesia-related drugs are also one of the risk factors affecting PONV. Compared with other anesthesia methods, the incidence of PONV was increased under general anesthesia, and the combination of intravenous anesthesia and intraoperative opioid application also increased the incidence of postoperative nausea and vomiting. 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 study will explore the preventive effect of stellate ganglion block on postoperative nausea and vomiting in gynecological laparoscopic patients, and hope to explore its possible mechanism, so as to provide more effective and feasible methods for clinical prevention of postoperative nausea and vomiting and improve patients' medical comfort and satisfaction.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Right-stellate ganglion block
The experimental group was given right stellate ganglion block 30 minutes before anesthesia

Locations

Country Name City State
China The Second Affiliated Hospital of Chongqing Medical University Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
The Second Affiliated Hospital of Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome

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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