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Trial registered on ANZCTR
Registration number
ACTRN12624000248561
Ethics application status
Approved
Date submitted
12/12/2023
Date registered
13/03/2024
Date last updated
13/03/2024
Date data sharing statement initially provided
13/03/2024
Type of registration
Retrospectively registered
Titles & IDs
Public title
The efficacy of ondansetron as an adjunct to lidocaine compared with lidocaine pretreatment in reducing pain on propofol injection: A randomized controlled trial
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Scientific title
The efficacy of ondansetron as an adjunct to lidocaine compared with lidocaine pretreatment in reducing pain on propofol injection: A randomized controlled trial.
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Secondary ID [1]
311157
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nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pain on propofol injection
332321
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Condition category
Condition code
Anaesthesiology
329031
329031
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0
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Pain management
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
20mg lidocaine (2% preservative-free) with 4mg ondansetron was prepared and was administered intravenously at the 3-way stop cock in 5 seconds by the nurse then the 3-way stop cock was locked for 15 seconds before 50 mg of propofol was administered in 5 seconds by the anesthesiologist.
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Intervention code [1]
327598
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Treatment: Drugs
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Comparator / control treatment
20mg lidocaine (2% preservative-free) was prepared and was administered intravenously at the 3-way stop cock in 5 seconds by the nurse then the 3-way stop cock was locked for 15 seconds before 50 mg of propofol was administered in 5 seconds by the anesthesiologist.
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Control group
Active
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Outcomes
Primary outcome [1]
336840
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Pain on propofol injection
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Assessment method [1]
336840
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McCririck and Hunter Pain Scale
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Timepoint [1]
336840
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immediately after injection of propofol
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Secondary outcome [1]
429800
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Pain on propofol injection
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Assessment method [1]
429800
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McCririck and Hunter Pain Scale
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Timepoint [1]
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20 seconds after injection of propofol
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Secondary outcome [2]
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adverse effects of ondansetron
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Assessment method [2]
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observe EKG if there is QT prolong, observe skin reaction if there is rash.
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Timepoint [2]
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After injection until leave PACU
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Secondary outcome [3]
431506
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adverse effects of lidocaine
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Assessment method [3]
431506
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observe EKG for bradycardia or arrhythmia, rash on skin
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Timepoint [3]
431506
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After injection until leave PACU
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Eligibility
Key inclusion criteria
-ASA classification I-II
-scheduled for elective surgery with general anesthesia
-Age 18- 60 years old
-Weight more than 50 kg.
-cooperate and able to communicate
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Minimum age
18
Years
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Maximum age
60
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
-patient's refusal
-did not use propofol as induction agent
-IV catheter 20G can't be accessed
-local infection at IV site
-Allergic to ondansetron or lidocaine
-History of cardiac arrhythmia
-unable to assess the pain score
-chronic pain or receive analgesic 24 hours before surgery
-RSI technique was used
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
sealed envelop
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
a randomisation table created by computer software (i.e. computerised sequence generation), Block of 4
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
3/08/2023
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Date of last participant enrolment
Anticipated
31/07/2024
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Actual
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Date of last data collection
Anticipated
31/07/2024
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Actual
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Sample size
Target
260
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Accrual to date
50
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Final
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Recruitment outside Australia
Country [1]
26030
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Thailand
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State/province [1]
26030
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Bangkok
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Funding & Sponsors
Funding source category [1]
315411
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Hospital
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Name [1]
315411
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King Chulalongkorn Memorial Hospital
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Address [1]
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none
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Country [1]
315411
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Thailand
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Primary sponsor type
Hospital
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Name
King Chulalongkorn Memorial Hospital
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Address
none
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Country
Thailand
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Secondary sponsor category [1]
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None
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Name [1]
317475
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Address [1]
317475
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Country [1]
317475
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
314326
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The Institutional Review Board of the Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand,
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Ethics committee address [1]
314326
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1873 Rama IV Rd. Patumwan Patumwan Bangkok Thailand 10330
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Ethics committee country [1]
314326
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Thailand
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Date submitted for ethics approval [1]
314326
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19/04/2023
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Approval date [1]
314326
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22/06/2023
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Ethics approval number [1]
314326
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Summary
Brief summary
Ondansetron was proved to decrease pain on propofol injection. Lidocaine also has a role on pain on propofol injection. This study is aimed to determine efficacy of ondansetron as an adjunct to lidocaine in pain on propofol injection compared with lidocaine alone.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Ms Lucksamon Sirivichayakul
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Address
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Department of Anesthesiology, Faculty of Medicine , Chulalongkorn University, 1873 Rama IV Rd. Patumwan Patumwan Bangkok Thailand
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Country
131198
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Thailand
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Phone
131198
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+66825586332
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Fax
131198
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Email
131198
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[email protected]
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Contact person for public queries
Name
131199
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Lucksamon Sirivichayakul
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Address
131199
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Department of Anesthesiology, Faculty of Medicine , Chulalongkorn University, 1873 Rama IV Rd. Patumwan Patumwan Bangkok Thailand
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Country
131199
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Thailand
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Phone
131199
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+66825586332
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Fax
131199
0
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Email
131199
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[email protected]
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Contact person for scientific queries
Name
131200
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Lucksamon Sirivichayakul
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Address
131200
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Department of Anesthesiology, Faculty of Medicine , Chulalongkorn University, 1873 Rama IV Rd. Patumwan Patumwan Bangkok Thailand
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Country
131200
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Thailand
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Phone
131200
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+66825586332
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Fax
131200
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Email
131200
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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