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 |
| Secondary identifying numbers | 511007 |
- 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
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
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Scientific title | |
| Study hypothesis | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Condition | Spontaneous abortion |
| Intervention | Routine surgical evacuation or medical evacuation of the uterus using misoprostol |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Misoprostol |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/10/1995 |
| Overall study end date | 01/01/1998 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Female |
| Target number of participants | Not provided at time of registration |
| Participant 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) |
| Participant exclusion criteria | Does not meet inclusion criteria |
| Recruitment start date | 01/10/1995 |
| Recruitment end date | 01/01/1998 |
Locations
Countries of recruitment
- Hong Kong
Study participating centre
Department of Obstetrics & Gynaecology
-
-
Hong Kong
-
Hong Kong
Sponsor information
Hong Kong Health Services Research Fund (Hong Kong)
Government
Government
Health Welfare and Food Bureau
Government Secretariat, HKSAR
20th floor Murray Building
Garden Road
-
-
Hong Kong
| Phone | +852 (0)2973 8288 |
|---|---|
| hsrf@hwfb.gov.hk | |
| Website | http://www.fhb.gov.hk/grants/english/funds/funds_hhsrf/funds_hhsrf_abt/funds_hhsrf_abt.html |
"ROR" |
https://ror.org/03qh32912 |
Funders
Funder type
Government
Hong Kong Health Services Research Fund (Hong Kong)
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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/06/1999 | Yes | No |
