Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12615000872538
Ethics application status
Approved
Date submitted
15/06/2015
Date registered
21/08/2015
Date last updated
6/06/2016
Type of registration
Prospectively registered

Titles & IDs
Public title
Comparing two different concentrations of Intranasal Fentanyl in adults presenting to Frankston Emergency Department with moderate to severe pain.
Scientific title
A prospective randomized study comparing the efficacy of two different concentrations of Intranasal Fentanyl: the standard formulation (50mcg/mL) and the concentrated formulation (300mcg/mL) in adults presenting to Frankston Emergency Department (ED) with moderate to severe pain.
Secondary ID [1] 286909 0
Nil known
Universal Trial Number (UTN)
U1111-1171-1957
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
moderate to severe pain 295327 0
Condition category
Condition code
Anaesthesiology 295597 295597 0 0
Pain management

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Intranasal Fentanyl Standard Formulation (50mcg/mL)
Single Dose, administered by treating doctor immediately on arrival (patients with moderate to severe pain with pain score greater than or equal to 6 ). Administration of the medication will be witnessed by a nurse as well.
Intervention code [1] 292095 0
Treatment: Drugs
Comparator / control treatment
Intranasal Fentanyl Concentrated Formulation (300mcg/mL)
Single Dose, administered by treating doctor immediately on arrival (patients with moderate to severe pain - pain sore greater than or equal to 6 ). Administration of the medication will be witnessed by a nurse as well.
Control group
Dose comparison

Outcomes
Primary outcome [1] 295307 0
Mean change in Visual Analog Scale (VAS) pain score from pre-administration (T0) to 30 minutes post-administration (T30) in the Standard Intranasal Fentanyl (SINF) and Concentrated Intranasal Fentanyl (CINF) groups, and the difference in the means between the two groups. Composite outcome. Assessed from the patient scored VAS recorded on the data collection form.
Timepoint [1] 295307 0
Pain score (VAS) at 30 minutes post analgesia.
Secondary outcome [1] 315319 0
Mean change in Visual Analog Scale pain score from pre-administration (T0) to 15 minutes (T15) and 60 minutes (T60) post-administration and the difference in the means between the two groups.
Composite outcome. Assessed from the patient scored VAS recorded on the data collection form.
Timepoint [1] 315319 0
Pain score (VAS) at 15 and 60 minutes post analgesia.
Secondary outcome [2] 315320 0
Percentage requiring an additional dose of fentanyl at T15, and the difference between the two groups. Composite outcome. Assessed from the data recorded by the investigator on the data collection form.
Timepoint [2] 315320 0
Additional INF at 15 minutes post analgesia.
Secondary outcome [3] 315321 0
Compare Adverse event profiles in the two groups. Examples of known adverse events are: Over-sedation. This will be monitored by the treating doctor, using the Ramsay sedation scale. Nausea and vomiting. These will be monitored by the study doctor as per standard patient care and anti-emetics may be indicated. Assessed from the data recorded by the investigator on the data collection form.
Timepoint [3] 315321 0
any time an adverse event occurs from the time of drug administration until T60

Eligibility
Key inclusion criteria
1. Age 18 years to 75 years of age
2. Self-report pain severity as being 6 or more on the standard 10 point verbal rating scale (0 is none, 10 is worst pain imaginable)
3. Medical recommendation for parenteral analgesia (treating doctor’s discretion)
4. Pain from any cause other than the 3 specific exclusions (see below)
Minimum age
18 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Known allergy or previous adverse reaction to fentanyl
2. Patients over 75 years of age
3. Use of oral, intranasal, transdermal or parenteral narcotic analgesia in previous 4 hours (either pre-hospital or in the emergency department) [NB. Pre-hospital use of short-acting inhaled methoxyfluorane alone or non-narcotic analgesics do not constitute an exclusion]
4. MAO Inhibitor antidepressant use within last 14 days
5. Myasthenia gravis
6. Haemodynamic instability (eg HR over 120/min or BP under 90 mmHg) with the need for time critical interventions of any type
7. Suspicion of any of the following medical conditions:
myocardial ischaemia (concern re transient hypotension from fentanyl)
suspected subarachnoid haemorrhage (concern re transient hypotension from fentanyl)
migraine (specific proven therapy)
Relative contraindication to, or anticipated difficulty with nasal administration of medication that may prevent adequate administration or absorption of intranasal medication (eg aberrant nasal anatomy, acute or chronic nasal problems or nasal trauma).
Presence of acute cognitive impairment (any underlying cause)
Schizophrenia or related psychiatric conditions (even if currently well controlled)
History of recreational substance abuse
Inability to understand study explanation or procedures, or to provide informed consent
Pregnancy, breast feeding

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Once patient consent is obtained, the patient will be randomised into Group A (Standard INF, 50 mcg/mL) or Group B (Concentrated INF, 300 mcg/mL). The patient randomization list is prepared in advance by a member of the research team who will have no contact with patients and have no role in assigning patients to treatment groups. The randomization list is prepared using a computer-generated programme. A sealed envelope attached to each study pack will contain the allocation group, and study packs will be used sequentially.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomization list was prepared using a computer-generated programme.
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Type of endpoint/s
Efficacy
Statistical methods / analysis
Baseline data including age, sex, weight and diagnosis will be described as median with interquartile range and number with percentage as appropriate. Pain and sedation scores at each time point will be described as median with interquartile range. Change in VAS score from T0 to each other time point will be described as mean reduction (with ‘positive’ being shift towards the left of the scale) in millimetres with 95% confidence interval. The difference in the mean VAS reduction scores between the two groups will be assessed using a Mann Whitney U test. Change in sedation scores will be described as median change with interquartile range. The other categorical outcomes of descriptions of amount of change and satisfaction will be described as number and percentage, as will be adverse events of different types. Some comparison of outcome measures between those who received only the initial 1.4 mcg/kg fentanyl dose and those who received the additional 0.7 mcg/kg dosage at T15 may be performed depending on frequency of the latter dosage addition.
Sample size calculations: There is general literature agreement that the clinically significant reduction in severe pain score is between 15-30 mm on the 10cm visual analog scale. Based on the available literature and the mean change and standard deviation derived from an earlier pilot study, power of 0.8, alpha of 0.05, a sample of 45 patients per group would be required to detect a difference in reduction of VAS score by 15 mm. Recruitment of 110 patients (55 per group) would allow a further 20% 'leeway' to cover the patient drop-outs, incomplete data etc.

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
1/09/2015
Actual
15/03/2016
Date of last participant enrolment
Anticipated
30/08/2017
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
110
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 3920 0
Frankston Hospital - Frankston
Recruitment postcode(s) [1] 9838 0
3199 - Frankston

Funding & Sponsors
Funding source category [1] 291467 0
Hospital
Name [1] 291467 0
Peninsula Health
Country [1] 291467 0
Australia
Primary sponsor type
Individual
Name
A/Prof Pamela Rosengarten
Address
Peninsula Health, Frankston Hospital Emergency Department
P O Box 52 Frankston VIC 3199
Country
Australia
Secondary sponsor category [1] 290147 0
Individual
Name [1] 290147 0
Dr Kishan Ajjampur
Address [1] 290147 0
Peninsula Health, Frankston Hospital Emergency Department
P O Box 52 Frankston VIC 3199
Country [1] 290147 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 293016 0
Peninsula Health Human Research Ethics Committee
Ethics committee address [1] 293016 0
Ethics committee country [1] 293016 0
Australia
Date submitted for ethics approval [1] 293016 0
19/06/2015
Approval date [1] 293016 0
13/01/2016
Ethics approval number [1] 293016 0
HREC/15/PH/17

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 58098 0
A/Prof Pamela Rosengarten
Address 58098 0
Frankston Hospital, Emergency department
P O Box 52
Frankston Vic 3199
Country 58098 0
Australia
Phone 58098 0
+61 3 9784 1682
Fax 58098 0
Email 58098 0
[email protected]
Contact person for public queries
Name 58099 0
Pamela Rosengarten
Address 58099 0
Frankston Hospital, Emergency Department
P O Box 52
Frankston, VIC 3199
Country 58099 0
Australia
Phone 58099 0
+61 3 97847777
Fax 58099 0
Email 58099 0
[email protected]
Contact person for scientific queries
Name 58100 0
Pamela Rosengarten
Address 58100 0
Frankston Hospital, Emergency Department
P O Box 52
Frankston, VIC 3199
Country 58100 0
Australia
Phone 58100 0
+61 3 9784 1682
Fax 58100 0
Email 58100 0
[email protected]

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No Supporting Document Provided



Results publications and other study-related documents

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