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Clinical Trial Details — Status: Withdrawn

Administrative data

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Status Withdrawn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

Study information

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

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Gabapentin
anticonvulsant drug that is used for neuropathic pain.
Procedure:
TAP Block
a procedure done anesthetize the anterior abdominal wall

Locations

Country Name City State
United States SUNY Downstate Medical Center Brooklyn New York

Sponsors (1)

Lead Sponsor Collaborator
State University of New York - Downstate Medical Center

Country where clinical trial is conducted

United States, 

Outcome

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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