A randomised, controlled clinical trial involving women who have aborted spontaneously; the health, social and operational costs, outcomes of conservative and routine management
| ISRCTN | ISRCTN43067169 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN43067169 |
| Protocol serial number | 511007 |
| Sponsor | Hong Kong Health Services Research Fund (Hong Kong) |
| Funder | Hong Kong Health Services Research Fund (Hong Kong) |
- Submission date
- 10/10/2002
- Registration date
- 10/10/2002
- Last edited
- 02/07/2009
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Pregnancy and Childbirth
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr TKH Chung
Scientific
Scientific
Department of Obstetrics & Gynaecology
Prince of Wales Hospital
Chinese University of Hong Kong
-
-
Hong Kong
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Spontaneous abortion |
| Intervention | Routine surgical evacuation or medical evacuation of the uterus using misoprostol |
| Intervention type | Drug |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Misoprostol |
| Primary outcome measure(s) |
Not provided at time of registration |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/01/1998 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Female |
| Key inclusion criteria | All women admitted to the gynaecological unit of the Prince of Wales Hospital from October 1995 to January 1998 with: 1. A clinical diagnosis of spontaneous abortion 2. A positive urinary pregnancy test, and 3. Transvaginal Sonography (TVS) evidence of retained Products Of Conception (POCs) |
| Key exclusion criteria | Does not meet inclusion criteria |
| Date of first enrolment | 01/10/1995 |
| Date of final enrolment | 01/01/1998 |
Locations
Countries of recruitment
- Hong Kong
Study participating centre
Department of Obstetrics & Gynaecology
-
-
Hong Kong
-
Hong Kong
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? |
|---|---|---|---|---|---|
| Results article | results | 01/06/1999 | Yes | No |
