Missed Abortion Clinical Trial
Official title:
Oxytocin Effectiveness in First Trimester Dilatation and Curettage - a Double Blind Placebo Controlled Randomized Trial
Verified date | June 2024 |
Source | Assuta Ashdod Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this study is to investigate the impact of oxytocin on perioperative blood loss during the D&C procedure, as well as to assess early and late complications associated with it's use.
Status | Not yet recruiting |
Enrollment | 160 |
Est. completion date | June 2026 |
Est. primary completion date | June 2026 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All patients admitted to the OBGYN Assuta Ashdod Hospital for elective surgical termination of pregnancy due to missed miscarriages in the first trimester, with gestational age range of 6.0 to 11.6 weeks. Patients aged 18 years and older who are capable to provide informed consent. Exclusion Criteria: - individual intolerance to oxytocin - mullerian anomalies - Fibroid uterus - thrombophilia or coagulation disorders - cardiovascular disease |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Assuta Ashdod Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Perioperative Blood Loss Assessment | We will assess perioperative blood loss by:
Measuring the content collected in the vacuum apparatus after the procedure. Recording hemoglobin and hematocrit levels prior to the procedure. Measuring hemoglobin and hematocrit levels immediately after the procedure. Monitoring hemoglobin and hematocrit levels three days post-procedure. |
3 days | |
Secondary | perioperative complications according to the Dindo-Clavien scale | perioperative complications according to the Dindo-Clavien scale | 3 days |
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