Postoperative Pain Clinical Trial
Official title:
Combination of Preoperative Gabapentin and TAP Blocks in Decreasing Postoperative Pain
NCT number | NCT02927405 |
Other study ID # | 926072 |
Secondary ID | |
Status | Withdrawn |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | March 4, 2020 |
Est. completion date | March 31, 2020 |
Verified date | May 2021 |
Source | State University of New York - Downstate Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
There is an increasing trend on decreasing narcotic use and maximizing efficiency in the perioperative care. There are no studies that have compared a TAP block versus a TAP block plus gabapentin for laparoscopic procures.This study will investigate if taking gabapentin and receiving a TAP block decrease post-operative morphine consumption. It will be a randomized controlled, double blind study, with 130 patients between 18-60 years; that will undergo laparoscopic GYN procedures. Secondary outcomes will look at the incidence of nausea, vomiting, and VAS (verbal analog scale) scores. This combination may be helpful because gabapentin will be used to decrease visceral and central pain, and TAP block will decrease somatic pain. Performing a multimodal approach may decrease narcotic consumption, adverse effects and improve pain management.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 31, 2020 |
Est. primary completion date | March 31, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - female - receiving laparoscopic GYN procedure - between 18-60 Exclusion Criteria: - are already taking gabapentin - have diabetic neuropathy - have a chronic pain syndrome - take opioids at home - are pregnant - have kidney disease - have an allergy to morphine |
Country | Name | City | State |
---|---|---|---|
United States | SUNY Downstate Medical Center | Brooklyn | New York |
Lead Sponsor | Collaborator |
---|---|
State University of New York - Downstate Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Incidence of nausea and vomiting | How many times the patient reported nausea, and how many times they vomitted. | 24 hours after surgery | |
Primary | Post-operative morphine consumption | Total amount of morphine the patient need to control post-operative pain | 24 hours after surgery. | |
Secondary | VAS Scores | Visual analog scale that rates a patient's pain | 24 hours after surgery |
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