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Trial registered on ANZCTR
Registration number
ACTRN12624000527561
Ethics application status
Approved
Date submitted
23/12/2023
Date registered
28/04/2024
Date last updated
28/04/2024
Date data sharing statement initially provided
28/04/2024
Type of registration
Retrospectively registered
Titles & IDs
Public title
Postoperative analgesic efficacy of intrathecal Nalbuphine with Bupivacaine in
spinal anesthesia for anorectal surgery : A randomized controlled trial
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Scientific title
Postoperative analgesic efficacy of intrathecal Nalbuphine with Bupivacaine in
spinal anesthesia for anorectal surgery : A randomized controlled trial
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Secondary ID [1]
311143
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None
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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:
Postoperative pain after anorectal surgery
332361
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Condition category
Condition code
Anaesthesiology
329070
329070
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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
0.5% hyperbaric bupivacaine 1.5-2ml (7.5-10 mg) mixed with Nalbuphine 0.3 mg intrathecal (intervention) intrathecal by anesthetist or anesthesia resident once only just before surgery
(dose based on Gudaityte J, Marchertiene I, Pavalkis D, Saladzinskas Z, Tamelis A, Toker I. Minimal effective dose of spinal hyperbaric bupivacaine for adult anorectal surgery: a prospective, double-blinded, randomized study: A-362. European Journal of Anaesthesiology | EJA. 2005;22:96.))
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Intervention code [1]
327639
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Treatment: Drugs
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Comparator / control treatment
0.5% hyperbaric bupivacaine 1.5-2ml (7.5-10 mg) alone (current standard treatment) intrathecal by anesthetist or anesthesia resident once only just before surgery
(dose based on Gudaityte J, Marchertiene I, Pavalkis D, Saladzinskas Z, Tamelis A, Toker I. Minimal effective dose of spinal hyperbaric bupivacaine for adult anorectal surgery: a prospective, double-blinded, randomized study: A-362. European Journal of Anaesthesiology | EJA. 2005;22:96.))
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Control group
Active
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Outcomes
Primary outcome [1]
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postoperative pain score at rest
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Assessment method [1]
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visual analogue scale
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Timepoint [1]
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12 hours after administration of spinal anesthesia
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Primary outcome [2]
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postoperative pain score on motion
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Assessment method [2]
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visual analogue scale
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Timepoint [2]
337569
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12 hours after administration of spinal anesthesia
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Secondary outcome [1]
430048
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time to first analgesia required
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Assessment method [1]
430048
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record the first time that patient ask for other pain medication after spinal anesthesia (as hours)
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Timepoint [1]
430048
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From administration of spinal anaesthesia to 24 hours after spinal anaesthesia
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Secondary outcome [2]
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types and amount of analgesia required after spinal anesthesia
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Assessment method [2]
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record type, amount and timing of analgesia require after spinal anesthesia from medical records
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Timepoint [2]
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From administration of spinal anaesthesia to 24 hours after spinal anaesthesia
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Secondary outcome [3]
430051
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possible adverse effects from spinal Nalbuphine (composite outcome)
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Assessment method [3]
430051
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record possible signs and symptoms of adverse effects such as hypotension (systolic blood pressure < 90 mmHg or decrease more than 20% of baseline blood pressure), nausea and vomitting (score 0-3 from none to severe), pruritus (score 0-3 from none to severe), sedation score (Ramsay sedation scale from 1-6), urinary retention (time to first spontaneous voiding, urinary retention symptoms and time when catheterization if occur) from medical records
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Timepoint [3]
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From administration of spinal anaesthesia to 24 hours after spinal anaesthesia
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Eligibility
Key inclusion criteria
1. patients under going elective anorectal surgery under spinal anesthesia at King Chulalongkorn Memorial Hospital age from 18 to 65 year old
2. American Society of Anesthesiologists Physical Status I to II
3. patients consented to participate in our research
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Minimum age
18
Years
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Maximum age
65
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
1. patients that have history of allergy to research drugs
2. patients that can't report their pain score
3. patients with history of chronic pain (more than 3 months) and have history of morphine use
4. patients with skin disease or preopearive pruritic symptoms
5. patients that require postoperative intentive care unit
6. patients contraindicated to spinal anesthesia
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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 opaque envelope
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomized by computer
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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
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 4
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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
22/09/2023
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Date of last participant enrolment
Anticipated
30/04/2024
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Actual
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Date of last data collection
Anticipated
30/04/2024
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Actual
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Sample size
Target
90
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Accrual to date
35
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Final
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Recruitment outside Australia
Country [1]
26038
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Thailand
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State/province [1]
26038
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Khet Pathum Wan
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Funding & Sponsors
Funding source category [1]
315457
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Self funded/Unfunded
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Name [1]
315457
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Nantapat Soonthonnitikul
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Address [1]
315457
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1701 Chomfah village Rangsit-Nakornnayok 64 alley, Rangsit-Nakornnayok road, Prachatiput, Tanyaburi, Pathumtani 12130
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Country [1]
315457
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Thailand
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Primary sponsor type
Individual
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Name
Nantapat Soonthonnitikul
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Address
1701 Chomfah village Rangsit-Nakornnayok 64 alley, Rangsit-Nakornnayok road, Prachatiput, Tanyaburi, Pathumtani 12130
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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]
317525
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Address [1]
317525
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Country [1]
317525
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
314316
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Institutional review boards, Faculty of Medicine, Chulalongkorn university
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Ethics committee address [1]
314316
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1873, Rama 4 Road, Pathumwan, Bangkok 10330
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Ethics committee country [1]
314316
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Thailand
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Date submitted for ethics approval [1]
314316
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21/07/2023
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Approval date [1]
314316
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22/08/2023
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Ethics approval number [1]
314316
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0393/66
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Summary
Brief summary
- primary hypothesis : patients undergoing elective anorectal surgery under spinal anesthesia with 0.5% hyperbaric bupivacaine 7.5-10 mg with spinal Nalbuphine 0.3 mg will have lesser pain score than controlled group -secondary hypothesis : spinal anesthesia with 0.5% hyperbaric bupivacaine 7.5-10 mg with spinal Nalbuphine group will have the same incidence of adverse effects and complication such as nausea, vomitting, pruritus, sedative effect and urinary retention as contolled group
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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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Dr Nantapat Soonthonnitikul
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Address
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King Chulalongkorn Memorial Hospital, 1873 Rama IV Rd, Pathum Wan, Bangkok 10330
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Country
131158
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Thailand
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Phone
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+66856999880
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Fax
131158
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Email
131158
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[email protected]
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Contact person for public queries
Name
131159
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Nantapat Soonthonnitikul
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Address
131159
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King Chulalongkorn Memorial Hospital, 1873 Rama IV Rd, Pathum Wan, Bangkok 10330
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Country
131159
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Thailand
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Phone
131159
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+66856999880
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Fax
131159
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Email
131159
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[email protected]
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Contact person for scientific queries
Name
131160
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Nantapat Soonthonnitikul
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Address
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King Chulalongkorn Memorial Hospital, 1873 Rama IV Rd, Pathum Wan, Bangkok 10330
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Country
131160
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Thailand
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Phone
131160
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+66856999880
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Fax
131160
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Email
131160
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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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