A cohort study to investigate the relationship between Analgesia Nociception Index and local anesthetic infiltration pain in pregnant women undergoing elective cesarean sectio
Not Applicable
Recruiting
- Conditions
- A pregnant woman undergoing elective cesarean delivery
- Registration Number
- JPRN-UMIN000045935
- Lead Sponsor
- School of medicine, Kitasato university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who have difficulty or inability to communicate Patients who are scheduled to undergo cesarean delivery with general anesthesia Patients who are allergic to local anesthetics Patients who are in some kind of pain. Patients who are taking analgesic medication. Patients who are chronically taking medication (except for supplements such as vitamins) Patients with psychiatric disorders Patients with preoperative ECG abnormalities Patients with hypertensive disorder of pregnancy Patients with BMI above 35
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To investigate the thresholds of the analgesia nociception Index, which discriminates the severity of local anesthetic infiltration pain as assessed by the Verbal Numerical Rating Scale.
- Secondary Outcome Measures
Name Time Method To investigate the relationship between Analgesia Nociception Index and local anesthetic infiltration pain.