Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12609001028291
Ethics application status
Approved
Date submitted
19/11/2009
Date registered
27/11/2009
Date last updated
27/11/2009
Type of registration
Prospectively registered

Titles & IDs
Public title
The effect of chitosan spray on bleeding and wound healing following tear duct surgery.
Scientific title
A single centre, prospective, randomised, comparative interventional case series investigating the effect of topical chitosan spray on haemostasis and wound healing following endoscopic dacryocystorhinostomy (endoDCR) without intubation in patients with primary acquired nasolacrimal duct obstruction.
Secondary ID [1] 1146 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
To evaluate the effect of topical chitosan spray on haemostasis and wound healing following endoscopic dacryocystorhinostomy (endoDCR) without intubation. 252245 0
Condition category
Condition code
Eye 252432 252432 0 0
Diseases / disorders of the eye

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Prospective, randomised, comparative interventional case series, comparing patients who receive chitosan spray at the end of endoDCR with patients who do not receive chitosan spray (controls).

Chitosan is a compound made from substances called dextran and chitosan ( a product of squid skeletons), which are broken down by the body over a few days and excreted in the urine. There have been no reported adverse effects these substances.

Chitosan is present in a number of “over-the-counter” medications marketed to reduce obesity. It is also a component of many cosmetics.

All patients presenting with epiphora (watery eyes) will undergo ophthalmological and nasal endoscopic examination. Only patients whose epiphora is secondary to a blocked nasolacrimal duct as confirmed by clinical testing (examination and syringing of the tear ducts) in addition to radiological imaging (dacryocystography -/+ lacrimal scintigraphy) will be included in the study. The nasal endoscopic examination will be performed to assess suitability for the endoDCR approach.

The surgery will be performed by a single surgeon (Professor Selva). The surgery will before in the Royal Adelaide Hospital eye theatre. During the surgery, the patient will be computer randomised to receive either chitosan spray or no spray. At the end of the procedure 1ml chitosan will be sprayed over the site of the surgery in the nose, in those randomised to receive it. There will only be a single dose of chitosan administered in the trial.

Follow-up will be at 1 week, 4 weeks and 3 months. At each follow-up endoscopic dye test and syringing will be performed in the clinic. A grading chart for the endoscopic examination will also be completed at each clinic visit. The chart will record the presence of blood clots, crusting at the site of the surgery, evidence of infection in the nose, mucosal oedema (swelling of the nose lining) and granulation tissue in the nose (scar tissue).
Intervention code [1] 241578 0
Treatment: Drugs
Comparator / control treatment
The surgery will be performed by a single surgeon (Professor Selva). The surgery will before in the Royal Adelaide Hospital eye theatre. During the surgery, the patient will be computer randomised to receive either chitosan spray or no spray. There will be no placebo. At the end of the procedure 1 ml of chitosan will be sprayed over the site of the surgery in the nose, in those randomised to receive it.

Follow-up will be at 1 week, 4 weeks and 3 months. At each follow-up endoscopic dye test and syringing will be performed in the clinic. A grading chart for the endoscopic examination will also be completed at each clinic visit. The chart will record the presence of blood clots, crusting at the site of the surgery, evidence of infection in the nose, mucosal oedema (swelling of the nose lining) and granulation tissue in the nose (scar tissue).
Control group
Active

Outcomes
Primary outcome [1] 253308 0
Comparison of the ostial patency and the positive endoscopic dye test at 3 months post operatively between the patients who received a single dose of 1ml chitosan (in spray form) at the time of surgery with those patients who received no spray (controls).
Timepoint [1] 253308 0
3 months post surgery
Primary outcome [2] 253328 0
The ostial patency rate in patients who underwent a single single dose of 1ml chitosan (in spray form) at the time of surgery should be better than patients who received no spray (controls). The ostial size should be bigger in the patients who underwent a single single dose of 1ml chitosan (in spray form) at the time of surgery than patients who received no spray (controls).

Patients will be assessed at each follow-up by perfroming a nasal endoscopic dye test in addition to syringing of the nasaolacrimal duct. A grading chart for the endoscopic examination will also be completed at each clinic visit. The chart will record the presence of blood clots, crusting at the site of the surgery, evidence of infection in the nose, mucosal oedema (swelling of the nose lining) and granulation tissue in the nose (scar tissue).
Timepoint [2] 253328 0
3 months post surgery
Secondary outcome [1] 262352 0
Comparison of the symptomatic relief from epiphora at 3 months between the patients who received chitosan spray with those patients who received no spray (controls).

At each follow-up endoscopic dye test and syringing will be performed in the clinic. The patient will also be asked if the symptom of epiphora (watering) has resolved/ improved or remains unchanged.
Timepoint [1] 262352 0
3 months post surgery
Secondary outcome [2] 262406 0
The incidence of a watery eye following surgery should be less in the patients who underwent a single single dose of 1ml chitosan (in spray form) at the time of surgery than patients who received no spray (controls).

Patients will be assessed at each follow-up by perfroming a nasal endoscopic dye test in addition to syringing of the nasaolacrimal duct. A grading chart for the endoscopic examination will also be completed at each clinic visit. The chart will record the presence of blood clots, crusting at the site of the surgery, evidence of infection in the nose, mucosal oedema (swelling of the nose lining) and granulation tissue in the nose (scar tissue).
Timepoint [2] 262406 0
3 months post surgery

Eligibility
Key inclusion criteria
All patients over the age of 18 years, who are able to give written informed consent.

All patients with primary acquired nasolacrimal duct obstruction (PANLDO) as confirmed by clinical examination and radiological investigations (dacryocystography -/+ lacrimal scintigraphy).

Adequate renal function (glomerular filtration calculated by Cockcroft/Gault formula or measure urine creatinine clearance > or = to 50 mL/minute)
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
All patients with canalicular disease (obstruction/ stenosis), found either pre-operatively or at the time of surgery.

All patients with a history of previous nasolacrimal surgery (DCR).

All patients not willing to participate in the study.

Any patient with an allergy to shell/fish as this compound is a product of squid skeletons.

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)
During the surgery, the patient will be computer randomised to receive either chitosan spray or no spray. At the end of the procedure chitosan will be sprayed over the site of the surgery in the nose, in those randomised to receive it.

Allocation is not concealed.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Random number generation by computer
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 2
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
4/01/2010
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
26
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 244057 0
Hospital
Name [1] 244057 0
South Australian Institute of Ophthalmology
Country [1] 244057 0
Australia
Primary sponsor type
Hospital
Name
South Australian Institute of Ophthalmology
Address
Discipline of Ophthalmology & Visual Sciences

Level 8
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
Country
Australia
Secondary sponsor category [1] 251404 0
None
Name [1] 251404 0
Address [1] 251404 0
Country [1] 251404 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 258152 0
Royal Adelaide Hospital
Ethics committee address [1] 258152 0
Ethics committee country [1] 258152 0
Australia
Date submitted for ethics approval [1] 258152 0
19/11/2009
Approval date [1] 258152 0
Ethics approval number [1] 258152 0

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

Contacts
Principal investigator
Name 30532 0
Address 30532 0
Country 30532 0
Phone 30532 0
Fax 30532 0
Email 30532 0
Contact person for public queries
Name 13779 0
Kylie Dansie
Address 13779 0
Discipline of Ophthalmology & Visual Sciences
South Australian Institute of Ophthalmology
Level 8
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
Country 13779 0
Australia
Phone 13779 0
+61 8 8222 2732
Fax 13779 0
+61 8 8222 2741
Email 13779 0
[email protected]
Contact person for scientific queries
Name 4707 0
Paul S Cannon
Address 4707 0
Discipline of Ophthalmology & Visual Sciences
South Australian Institute of Ophthalmology
Level 8
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
Country 4707 0
Australia
Phone 4707 0
+61 8 8222 2729
Fax 4707 0
+61 8 8222 2741
Email 4707 0
[email protected]

No information has been provided regarding IPD availability


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.