miscarriage retained products of conception
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with a miscarriage treated with misoprostol, and sonographic evidence of remnant of the miscarriage at the follow-up visit 7 days after initial treatment.
Exclusion criteria
Exclusion criteria: Women aged below 18 years Women with severe vaginal bleeding Women with severe abdominal pain Women with fever (> 38.0) or sepsis requiring antibiotic treatment and curettage, Women with contraindications for curettage Women with a failed misoprostol-induced miscarriage, as substantiated by the sonographic finding of an intact gestational sac still in situ.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the success rate in reaching an empty uterus, as substantiated by normal sonographic findings. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are Quality of Life scores assessed with the SF-36, the need of additional treatments, complications, quality of recovery pain and costs. | — |
Countries
Netherlands