Conscious Sedation for Cataract Operations Under Topical Anaesthesia
Primary Purpose
Conscious Sedation
Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Nalbuphine
Propofol
Dexmedetomidine
Benoxinate Hydrochloride 0.4% Eye Drops
Sponsored by
About this trial
This is an interventional other trial for Conscious Sedation
Eligibility Criteria
Inclusion Criteria:
- Both genders,
- 20 and 65 years,
- American Society of Anesthesiologists (ASA) physical status I and II,
- Scheduled for cataract extraction surgery under topical anaesthesia.
Exclusion Criteria:
- Known allergy to local anaesthetics,
- Allergy to study drugs,
- Second or third-degree heart block,
- Alcohol or drug abuse
- Morbid obesity, pregnant and lactating females,
- Patients with severe cardiac, renal and hepatic disorders.
Sites / Locations
- Faculty of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Group P
Droup D
Arm Description
nalbuphine/propofol group
Nalbuphine/dexmedetomidine group
Outcomes
Primary Outcome Measures
Sedation score
The degree of sedation assessed by Ramsay sedation score(1 = anxious, agitated, restless;2 = cooperative, oriented, tranquil; 3 = responds to commands only; 4 = brisk response to light glabellar tap or loud noise; 5 = sluggish response to light glabellar tap or loud noise; 6 = no response), score of (1) means inadequate sedation. Score (2 to 4) indicates acceptable sedation. Score (5) or (6) excessive sedation.
Secondary Outcome Measures
Heart rate
Heart rate in beats/minutes
Mean arterial blood pressure
Mean arterial blood pressure in mmHg
Oxygen saturation
Arterial oxygen saturation as a percentage of the total haemoglobin
Analgesia
Measured by Numerical Pain Rating scale where the patient verbally rates pain from 0 "no pain" to 10 "worst imaginable pain"
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03933280
Brief Title
Conscious Sedation for Cataract Operations Under Topical Anaesthesia
Official Title
Nalbuphine/Dexmedetomidine Versus Nalbuphine/Propofol Conscious Sedation for Cataract Extraction Under Topical Anaesthesia: A Double-Blind Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
December 1, 2020 (Actual)
Study Completion Date
January 1, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Menoufia University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Topical anaesthesia of the eye for ophthalmologic procedures avoids pain and discomfort of local anaesthetic injection in the peribulbar or retrobulbar block so that patient comfortability is achieved. Sedation during topical anaesthesia of the eye is mostly required to achieve anxiolysis, amnesia and keeping the patient calm all through the procedure. In the present study, the investigators will investigate the effect of nalbuphine/dexmedetomidine versus nalbuphine/propofol on the sedation as a primary outcome, intra-operative, postoperative analgesia, vital signs, patient and surgeon satisfaction and side effects as secondary outcomes
Detailed Description
In both groups, the patients will receive i.v. nalbuphine 50 μg/kg. Patients in group D, will receive an i.v. loading dose of dexmedetomidine 1 μg/kg over 10 min followed by a maintenance infusion of 0.5 μg/kg/h. Patients in group P, will receive a bolus i.v. dose of propofol 0.5 mg/kg followed by an infusion started at 0.025 mg/kg/min .If sedation score was <3, rescue sedation with boluses of midazolam 0.01 mg/kg will be given. If the patient complained of pain (Numerical verbal pain rating scale ≥3) during the surgery, i.v. fentanyl 50 μg will be given as an intra-operative rescue analgesic and the surgeon will be instructed to use additional topical local anaesthetic eye drops if appropriate. After the completion of surgery, all infusions will be stopped, and the patients will be shifted to the postanaesthetic care unit (PACU) to be monitored for 2 hours before discharge.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Conscious Sedation
7. Study Design
Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
An independent anaesthesiologist not involved in the study will open the randomisation envelope just before the premedication and will prepare the appropriate drug-filled syringes according to the code and will not take part in the management and observations. (Syringes and infusion lines will be concealed by wrapping with an aluminium foil). A blinded investigator that will not be involved in the anaesthetic management of the patients, will collect the intra-operative and postoperative data.
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group P
Arm Type
Active Comparator
Arm Description
nalbuphine/propofol group
Arm Title
Droup D
Arm Type
Active Comparator
Arm Description
Nalbuphine/dexmedetomidine group
Intervention Type
Drug
Intervention Name(s)
Nalbuphine
Other Intervention Name(s)
Nalbuphine bolus
Intervention Description
i.v. nalbuphine bolus of 50 μg/kg.
Intervention Type
Drug
Intervention Name(s)
Propofol
Other Intervention Name(s)
propofol infusion
Intervention Description
A bolus i.v. dose of propofol 0.5 mg/kg followed by an infusion of 0.025 mg/kg/min
Intervention Type
Drug
Intervention Name(s)
Dexmedetomidine
Other Intervention Name(s)
Dexmedetomidine infusion
Intervention Description
i.v. loading dose of dexmedetomidine 1 μg/kg over 10 min followed by a maintenance infusion of 0.5 μg/kg/h.
Intervention Type
Drug
Intervention Name(s)
Benoxinate Hydrochloride 0.4% Eye Drops
Other Intervention Name(s)
Topical anaesthesia of the eye
Intervention Description
Benoxinate hydrochloride 0.4% eye drops instilled twice, 5 minutes apart.
Primary Outcome Measure Information:
Title
Sedation score
Description
The degree of sedation assessed by Ramsay sedation score(1 = anxious, agitated, restless;2 = cooperative, oriented, tranquil; 3 = responds to commands only; 4 = brisk response to light glabellar tap or loud noise; 5 = sluggish response to light glabellar tap or loud noise; 6 = no response), score of (1) means inadequate sedation. Score (2 to 4) indicates acceptable sedation. Score (5) or (6) excessive sedation.
Time Frame
perioperative
Secondary Outcome Measure Information:
Title
Heart rate
Description
Heart rate in beats/minutes
Time Frame
perioperative
Title
Mean arterial blood pressure
Description
Mean arterial blood pressure in mmHg
Time Frame
perioperative
Title
Oxygen saturation
Description
Arterial oxygen saturation as a percentage of the total haemoglobin
Time Frame
perioperative
Title
Analgesia
Description
Measured by Numerical Pain Rating scale where the patient verbally rates pain from 0 "no pain" to 10 "worst imaginable pain"
Time Frame
perioperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Both genders,
20 and 65 years,
American Society of Anesthesiologists (ASA) physical status I and II,
Scheduled for cataract extraction surgery under topical anaesthesia.
Exclusion Criteria:
Known allergy to local anaesthetics,
Allergy to study drugs,
Second or third-degree heart block,
Alcohol or drug abuse
Morbid obesity, pregnant and lactating females,
Patients with severe cardiac, renal and hepatic disorders.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abd-Elazeem A Elbakry, MD
Organizational Affiliation
Associate professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Medicine
City
Cairo
State/Province
Shebin El-kom
ZIP/Postal Code
32511
Country
Egypt
12. IPD Sharing Statement
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Conscious Sedation for Cataract Operations Under Topical Anaesthesia
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