Do cycloplegics lessen the pain for a patient in the first 24 h following a corneal abrasion?
| ISRCTN | ISRCTN60648357 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN60648357 |
| Secondary identifying numbers | N0557119809 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 07/12/2015
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Injury, Occupational Diseases, Poisoning
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Ms Angela Clark
Scientific
Scientific
Specialist Registrar
Accident & Emergency Department
Russells Hall Hospital
Dudley
DY1 2HQ
United Kingdom
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Not specified |
| Study type | Treatment |
| Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet |
| Scientific title | Do cycloplegics lessen the pain for a patient in the first 24 h following a corneal abrasion? |
| Study objectives | Does the application of a topical cycloplegic have an effect upon the pain experienced by patients in the 24 h following a simple traumatic corneal abrasion? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Pain |
| Intervention | Prospective, double blinded, randomized controlled trial. Random allocation to: 1. Cyclopentolate 2. Normal saline |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Cyclopentolate |
| Primary outcome measure | Pain over the subsequent 24 h |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 14/01/2003 |
| Completion date | 31/07/2003 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 100 |
| Key inclusion criteria | 100 patients |
| Key exclusion criteria | Does not match inclusion criteria |
| Date of first enrolment | 14/01/2003 |
| Date of final enrolment | 31/07/2003 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Russells Hall Hospital
Dudley
DY1 2HQ
United Kingdom
DY1 2HQ
United Kingdom
Sponsor information
Department of Health (UK)
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.doh.gov.uk |
|---|
Funders
Funder type
Hospital/treatment centre
The Dudley Group of Hospitals NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not provided at time of registration |
| Publication and dissemination plan | Not provided at time of registration |
| IPD sharing plan |
Editorial Notes
07/12/2015: no publications found on PubMed.
