Actively Recruiting
Effects of Different Doses of Intravenous Lidocaine Infusion on Peri-operative Pain and Incidence of Postoperative Chronic Pain Within ERAS Protocols, a Dose Finding Study.
Led by Cairo University · Updated on 2024-05-28
69
Participants Needed
1
Research Sites
54 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aimed To investigate the effects of different doses of Intraoperative intravenous lidocaine infusion on intraoperative opioid consumption, perioperative pain control and incidence of postoperative chronic pain.
CONDITIONS
Official Title
Effects of Different Doses of Intravenous Lidocaine Infusion on Peri-operative Pain and Incidence of Postoperative Chronic Pain Within ERAS Protocols, a Dose Finding Study.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients age between 18 and 65.
- Patients with ASA I and II status.
- Patients undergoing open laparotomy surgeries (including open cholecystectomies).
You will not qualify if you...
- Patients unable to comprehend the informed consent.
- Patients on long term pre-operative opioid regimens.
- Patients with impairment in hepatic or renal functions.
- Patients who are planned to receive any form of regional block for the surgery.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Cairo University
Cairo, Egypt, 1111
Actively Recruiting
Research Team
A
Alaa Magdy Ahmed Hassan, Master
CONTACT
A
Amany Ezzat Ayad Ibrahim, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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