Low Pain Prediction in Cesarean Section Patients
Last updated on April 2022Recruitment
- Recruitment Status
- Terminated
- Estimated Enrollment
- 86
Inclusion Criteria
- not allergic to any study medications to be utilized in this study
- anticipated pain level estimated to be in the lowest 20th percentile (calculated <34.3 utilizing our standard preoperative questionnaire)
- age >/= 18
- ...
- not allergic to any study medications to be utilized in this study
- anticipated pain level estimated to be in the lowest 20th percentile (calculated <34.3 utilizing our standard preoperative questionnaire)
- age >/= 18
- singleton pregnancy
Exclusion Criteria
- diagnosis of a chronic pain disorder
- allergies to morphine or acetaminophen
- hepatic disease
- ...
- diagnosis of a chronic pain disorder
- allergies to morphine or acetaminophen
- hepatic disease
- weight >300 lbs
Summary
- Conditions
- Postoperative Pain Management
- Scheduled Cesarean Sections
- Side Effects
- Type
- Interventional
- Phase
- Phase 4
- Design
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Primary Purpose: Prevention
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Only females
Description
Subjects are randomized on the morning of surgery to receive a standard dose of spinal narcotic or to receive no long acting spinal narcotic. The subjects may or may not also receive acetaminophen orally postoperatively. Pain scores are done on postoperative day one as well as evaluation of potentia...
Subjects are randomized on the morning of surgery to receive a standard dose of spinal narcotic or to receive no long acting spinal narcotic. The subjects may or may not also receive acetaminophen orally postoperatively. Pain scores are done on postoperative day one as well as evaluation of potential narcotic side effects such as nausea/vomiting, itching, and sedation.
Inclusion Criteria
- not allergic to any study medications to be utilized in this study
- anticipated pain level estimated to be in the lowest 20th percentile (calculated <34.3 utilizing our standard preoperative questionnaire)
- age >/= 18
- ...
- not allergic to any study medications to be utilized in this study
- anticipated pain level estimated to be in the lowest 20th percentile (calculated <34.3 utilizing our standard preoperative questionnaire)
- age >/= 18
- singleton pregnancy
Exclusion Criteria
- diagnosis of a chronic pain disorder
- allergies to morphine or acetaminophen
- hepatic disease
- ...
- diagnosis of a chronic pain disorder
- allergies to morphine or acetaminophen
- hepatic disease
- weight >300 lbs
Tracking Information
- NCT #
- NCT02143141
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Jessica Booth, MD Wake Forest University Health Sciences
- Jessica Booth, MD Wake Forest University Health Sciences
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