Trials / Not Yet Recruiting
Not Yet RecruitingNCT06760130
Retrospective Evaluation of Infections After Delivery
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 150 (estimated)
- Sponsor
- IRCCS Azienda Ospedaliero-Universitaria di Bologna · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
In general, transabdominal and transvaginal ultrasound represent the first imaging method in the study of suspected postpartum infections because of its good sensitivity, low cost, and high safety for patients (in fact, it allows the patient to be studied at the bedside, even in clinically unstable patients, it is well tolerated by patients, and it has no risks). CT has an excellent sensitivity in the diagnosis of postpartum infections, however, it has some drawbacks: it is not an examination that can be performed in clinically unstable patients, it cannot be performed at the patient's bedside, it has high costs, and it involves the administration of a significant dose of radiation . There are conflicting data in the literature regarding which examination is most useful for the diagnosis/management of infections in postpartum. Therefore, the investigators want to evaluate whether ultrasound alone, compared with management with combined ultrasound and CT scan, is a useful and sufficient diagnostic tool for the diagnosis and management of postpartum infectious complications.
Detailed description
Cases of infection recorded as a result of these parts will be reviewed. Laboratory tests and clinical data of these will be reviewed. Instrumental, ultrasound and CT images taken in the postpartum for diagnostic confirmation and subsequent follow-up will also be reviewed. For each patient, information will be collected on: * Age, weight, height * Previous pregnancies and their outcome * Pregnancy that arose spontaneously or through Medically Assisted Procreation techniques * Conditions concomitant or complicating pregnancy * Pregnancy outcome (spontaneous delivery or cesarean section) * Laboratory tests * Clinical data collected during hospitalization (vital parameters, symptoms, any medications administered) * Radiologic (CT) or ultrasound (transabdominal and/or transvaginal) investigations performed during the hospital stay, in continuation-iter or in a subsequent hospitalization: name and model (and probe, for ultrasound examinations) of the equipment used will be specified for each examination performed.
Conditions
Timeline
- Start date
- 2025-01-01
- Primary completion
- 2026-12-31
- Completion
- 2026-12-31
- First posted
- 2025-01-06
- Last updated
- 2025-01-31
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT06760130. Inclusion in this directory is not an endorsement.