A trial of intranasal remifentanil for painful ophthalmic procedures.
Phase 1
- Conditions
- Painful ophthalmic procedures
- Registration Number
- EUCTR2006-002460-26-GB
- Lead Sponsor
- BHT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 78
Inclusion Criteria
Patients undergoing panretinal laser photocoagulation for diabetic retinopathy or cryotherapy for retinal holes.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Under 18 yrs age; under 50kg body weight.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: Determine whether effective pain relief is achieved;Secondary Objective: Acceptability to patients of the method of delivery;Primary end point(s): 78 patients teated.
- Secondary Outcome Measures
Name Time Method