NCT02801968UnknownNot Applicable
Tap Block and Cesarean Delivery: Efficacy and Consumption of Postoperative Drugs
S. Anna Hospital1 site in 1 country62 target enrollmentStarted: April 1, 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 62
- Locations
- 1
- Primary Endpoint
- Pain evaluation with Numerical Rating Scale (NRS)
Study Overview
Brief Summary
The purpose of this study is to determine the efficacy of Tap block after cesarean delivery as a component of multimodal analgesia and evaluation of postoperative drugs consumption.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •age > 18 years
- •written consent
- •anesthesiologist's assent on preoperative evaluation
Exclusion Criteria
- •age< 18 years
- •uncooperative patients
- •written consent not obtained
- •local anesthetic allergy
- •BMI > 35
Outcomes
Primary Outcomes
Pain evaluation with Numerical Rating Scale (NRS)
Time Frame: Pain evaluation with NRS at 2,6,12,24 hours after cesarean delivery in TAP block group and in the control group.
We don't want to measure the change between each assessment within a single group, instead we want considering the difference in the measurements between two separate groups (TAP block group and control group) for each time point.
Secondary Outcomes
- Evaluation of NSAIDs (nonsteroidal anti-inflammatory drugs) consumption as rescue dose during the first 24 hours after cesarean delivery(Doses of NSAIDs (nonsteroidal anti-inflammatory drugs) administered at 2, 6, 12 ,24 hours after cesarean delivery TAP block group and in the control group.)
Investigators
Ilaria Farinelli
Doctor
S. Anna Hospital
Study Sites (1)
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