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 |
| Protocol serial number | N0557119809 |
| Sponsor | Department of Health (UK) |
| Funder | The Dudley Group of Hospitals NHS Trust (UK) |
- 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
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Study type | Participant 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 |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Cyclopentolate |
| Primary outcome measure(s) | Pain over the subsequent 24 h |
| Key secondary outcome measure(s) | Not provided at time of registration |
| Completion date | 31/07/2003 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 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
- United Kingdom
- England
Study participating centre
Russells Hall Hospital
Dudley
DY1 2HQ
United Kingdom
DY1 2HQ
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
Editorial Notes
07/12/2015: no publications found on PubMed.
