An observational study in Placenta, Retained, Placenta; Retention, Fragments, Complicating Puerperium, Without Hemorrhage and Placenta; Retention, Fragments, Complicating Puerperium (Delayed Hemorrhage), sponsored by University Hospital, Ghent. Completed at 1 site in Belgium. Open to female participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-05-11.
Sponsored by University Hospital, Ghent · Observational
Collection of relevant data form patients who were treated in the Ghent University Hospital in the context of a placental remnant lager than 4 cm, performing statistical analyzes on the collected data, reviewing the literature on the subject and formulation of a recommendation for treatment of these large placental remnants.
University Hospital, Ghent is the lead sponsor of 685 studies on the registry; 158 are open to participants now.
Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) have results posted.
Counted across the registry records on this site, refreshed daily.
Patients with a placental remnant in medical history.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Procedure: kind of surgery
hysteroscopy, curettage, other
Hysteroscopy
Kind of surgery to remove retained products of conception
Time frame: time of surgery
Vacuum Curettage
Kind of surgery to remove retained products of conception
Time frame: time of curettage
Polyp forceps
Surgical instrument to remove retained products of conception
Time frame: time of surgery
Prostaglandines
Pharmacological agent to remove retained products of conception
Time frame: time of surgery
Ran from Dec 2020 to primary completion in Aug 2021, 8 months.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.
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Placenta, Retained