Clinical trial to obtain electrocardiaogram, pupillometry data for pain index development
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0001793
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 10
Pregnant women scheduled for vaginal delivery in Asan Medical Center
-Volunteer who consented to participate in the trial
-Any disease that affects autonomic nervous system (diabetes mellitus, catecholamine secreting tumor, depression etc.)
-Any disease that can induce spontaneous pain (rheumatoid arthritis, osteoarthritis, neuropathic pain inducing disease such as herniation of intervertebral disc and spinal stenosis), myopathic pain, or other chronic pain disease
-Blind person or other ophthalmic disease
-Arrhythmia or cardiac disease
-Cerebrovascular disease or prior brain surgery
-Epilepsy or history of psychosis
-Long term administration of sedatives
-Pregnant or possibly pregnant
-Patients who are considered by the investigator to be unsuitable to participate in the study for any other reason not mentioned in the inclusion and exclusion criteria.
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pupillometry and electrocardiogram measured during numeric rating scale for pain is over 5
- Secondary Outcome Measures
Name Time Method Pupillometry and electrocardiogram measured during numeric rating scale for pain is under 3;Adverse events