Anesthesia Clinical Trial
Official title:
A Pilot Study for a Prospective, Randomized Controlled Trial of Techniques for Perioperative Analgesia for Live Liver Donors
Verified date | January 2018 |
Source | Ain Shams University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study,will evaluate the efficacy of ultrasound (US)-guided subcostal oblique TAP block together with IV infusion of Dexmedetomidine and fentanyl as a type of multimodal analgesic regimen in comparison with IV fentanyl based analgesia only in live liver donors.
Status | Active, not recruiting |
Enrollment | 20 |
Est. completion date | February 2019 |
Est. primary completion date | December 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 50 Years |
Eligibility |
Inclusion Criteria: - American Society of Anesthesia (ASA) physical status I or II - Scheduled as live liver donors - J-shaped incision in the supraumblical region Exclusion Criteria: - Patients with a history of psychiatric/neurological illness, - Hypertensive patients, - Morbidly obese patients, - Pregnant and nursing women, - Patients with known allergic reaction to any of the study medications, - Patients on recent use of sedatives or analgesics, - Patients with significant laboratory abnormalities |
Country | Name | City | State |
---|---|---|---|
Egypt | Hospitals of Faculty of Medicine , Ain Shams University | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Total fentanyl consumption | Total Intravenous fentanyl consumption during the operation | Intraoperative | |
Secondary | Average sevoflurane concentration | The average sevoflurane concentration (the average concentration (%) for the case will be determined from the vaporizer setting recorded in the anesthetic record per 5-minute interval) | Intraoperative | |
Secondary | The severity of postoperative nausea and vomiting (PONV) | Will be recorded and classified as "no PONV, mild PONV, moderate PONV and severe PONV" | First 24 hours postoperatively | |
Secondary | Ramsay sedation score (RSS) | Will be used for assessment of sedation immediately after extubation, after 2 hours of ICU admission, after 12 hours then after 24 hours . | First 24 hours postoperatively |
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