European Randomised Trial of Ovarian Cancer Screening II
| ISRCTN | ISRCTN79217590 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN79217590 |
| Protocol serial number | ERTOCS II |
| Sponsor | Cancer Research UK (CRUK) (UK) |
| Funder | Cancer Research UK |
- Submission date
- 01/07/2001
- Registration date
- 01/07/2001
- Last edited
- 23/02/2015
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Cancer
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
Scientific
UKCCCR Register Co-ordinator
MRC Clinical Trials Unit
222 Euston Road
London
NW1 2DA
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | European Randomised Trial of Ovarian Cancer Screening II |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Ovarian cancer |
| Intervention | 1. Arm A: Vaginal ultrasound scan examination every 1.5 years 2. Arm B: Vaginal ultrasound scan examination every 3 years 3. Arm C: Control group - no scan |
| Intervention type | Other |
| Primary outcome measure(s) |
Not provided at time of registration |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 31/12/2000 |
Eligibility
| Participant type(s) | Healthy volunteer |
|---|---|
| Age group | Adult |
| Sex | Female |
| Key inclusion criteria | 1. All women aged 50-64 years 2. Before agreeing to join the trial, the women will have read the leaflet about the trial. |
| Key exclusion criteria | 1. Women already known to have ovarian cancer 2. Women who have had a bilateral oophorectomy |
| Date of first enrolment | 01/09/1993 |
| Date of final enrolment | 31/12/2000 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
MRC Clinical Trials Unit
London
NW1 2DA
United Kingdom
NW1 2DA
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | |
| IPD sharing plan |