Incomplete miscarriage
Conditions
Interventions
Randomise the study population into a surgical group where they will undergo evacuation of retained products of conception or an expectant group where they will be followed up weekly for six weeks cli
Sponsors
National Science Foundation
Eligibility
Inclusion criteria
Inclusion criteria: Women with an incomplete miscarriage with retained products less than 50mm AP diameter
Exclusion criteria
Exclusion criteria: Women with a strong preference for either intervention, women with profuse bleeding, severe pain or fever necessitating immediate surgical intervention will be exclude from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare the efficacy of surgical versus expectant management in incomplete miscarriage [] | — |
Secondary
| Measure | Time frame |
|---|---|
| Compare the efficacy of surgical versus expectant management in incomplete miscarriage [] | — |
Countries
Sri Lanka
Contacts
Public ContactDr Sanjeewa Padumadasa
Probationary Lecturer
Outcome results
None listed