To evaluate the effect of the contrast material used in hysterosalpingography (HSG) on subsequent reproductive success
| ISRCTN | ISRCTN12014186 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN12014186 |
| Secondary identifying numbers | N0072119582 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 14/02/2017
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Pregnancy and Childbirth
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
Dr Nikita Rawal
Scientific
Scientific
Countess of Chester NHS Foundation Trust
Liverpool Road
Chester
CH2 1UL
United Kingdom
| Phone | +44 (0)1244 366260 |
|---|---|
| nikitarawal@hotmail.com |
Study information
| Study design | Single blinded randomised controlled clinical trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Not specified |
| Study type | Not Specified |
| Scientific title | To evaluate the effect of the contrast material used in hysterosalpingography (HSG) on subsequent reproductive success |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Pregnancy and Childbirth: Fertility |
| Intervention | Women randomised at the time of HSG will either receive water soluble or oil soluble medium. |
| Intervention type | Other |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/01/2003 |
| Completion date | 31/12/2003 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Female |
| Target number of participants | 100 |
| Key inclusion criteria | Women who are having HSG for tubal patency. |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/2003 |
| Date of final enrolment | 31/12/2003 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Countess of Chester NHS Foundation Trust
Chester
CH2 1UL
United Kingdom
CH2 1UL
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
Government
Countess of Chester Hospital NHS Trust
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
14/02/2017: No publications found in PubMed, verifying study status with principal investigator.
