Use of mitomycin C to improve endonasal dacryocystorhinostomy (DCR) success rates
| ISRCTN | ISRCTN15566163 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN15566163 |
| Secondary identifying numbers | N0176108541 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 25/03/2020
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
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
Miss Germaine Gock
Scientific
Scientific
Oxford Eye Hospital
Radcliffe Infirmary
Woodstock Road
Oxford
OX2 6HE
United Kingdom
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Scientific title | Use of mitomycin C to improve endonasal dacryocystorhinostomy (DCR) success rates |
| Study objectives | A randomized controlled trial to determine whether intraoperative use of mitomycin C can improve the success rate of endonasal dacryocystorhinostomy (DCR) |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Dacryocystorhinostomy |
| Intervention | Mitomycin C vs standard practice |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | mitomycin C |
| Primary outcome measure | The patient being symptom free and/or patency to saline irrigation |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 25/01/2002 |
| Completion date | 30/06/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 20 patients and 20 control patients |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 25/01/2002 |
| Date of final enrolment | 30/06/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Oxford Eye Hospital
Oxford
OX2 6HE
United Kingdom
OX2 6HE
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.dh.gov.uk/Home/fs/en |
|---|
Funders
Funder type
Government
Oxford Radcliffe 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
25/03/2020: No publications found, all search options exhausted, study status unverified.
