Comparison Between Two Drugs (Propofol and Nitroglycerin as a Hypotensive Agents During Endoscopic Sinus Surgery
NCT ID: NCT04220281
Last Updated: 2020-02-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
PHASE1/PHASE2
40 participants
INTERVENTIONAL
2019-12-01
2020-02-12
Brief Summary
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Detailed Description
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One of the most important maneuvers used to minimize this bleeding is hypotensive anesthesia. The ideal hypotensive agent for anesthetist must be a familiar drug, easy to use, rapid onset and offset and with minimal side effects. Nitroglycerin infusion is a frequently used drug to produce controlled hypotension, as it is cheap and easy to use drug rapid onset and offset time. But a common side effect is reflex tachycardia and venous congestion which may also obscures the surgical filed and decreases surgeon satisfaction.
Total intravenous anesthesia (TIVA) using propofol and remifentanil is a common procedure used in western countries. In Egypt remifentanil is not freely available. So this study will be designed to use inhalational anesthesia and use propofol infusion as a hypotensive agent and to determine whether controlled hypotension, surgeon's satisfaction and better operative filed can be achieved when compared to nitroglycerine infusion.
2. AIM OF THE WORK The aim of the study is to identify the efficacy of propofol infusion as a hypotensive agent in comparison with nitroglycerin infusion during FESS.
Study Design
A total of 40 adult patients undergoing FESS procedure for sinusitis. Written informed consent will be obtained from all patients before randomization. Patients will be divided equally into two groups the first 20 patients will be assigned to propofol group (Prop group) and the other group to nitroglycerin group (NTG group). Group assignment, preparation and administration of drugs will be performed by a junior anesthetist who is neither involved nor interested by any means in the study. The patients, the ENT surgeon, and the anesthetist collecting data all were blind to the groups. The anesthetist performing the general anesthesia was not blinded to the drug given but he was not one of the study participants.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
TRIPLE
Study Groups
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propofol group
propofol group will receive propofol infusion
Propofol
propofol infusion during surgery
nitroglycerin group
will receive nitroglycerin infusion
Nitroglycerin
nitroglycerin infusion during surgery
Interventions
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Propofol
propofol infusion during surgery
Nitroglycerin
nitroglycerin infusion during surgery
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age range between 18-60 years, undergoing elective FESS without septoplasty under general anesthesia.
Exclusion Criteria
* renal, hepatic or cardiac dysfunction
* history of cerebrovascular stroke
* peripheral vascular diseases
* allergic to any of the study drugs
* hypertension
* morbid obesity and
* recurrent endoscopic sinus surgeries
18 Years
60 Years
ALL
Yes
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Rasha Gamal Abusinna
lecturer of anesthesia and intensive care, Principal Investigator
Principal Investigators
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Rasha G Abusinna, MD
Role: PRINCIPAL_INVESTIGATOR
Ain Shams University
Locations
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Ain Shams University Hospital
Cairo, EL Abassia, Egypt
Countries
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Other Identifiers
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RGAbusinna
Identifier Type: -
Identifier Source: org_study_id
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