Role of Doppler Echoflowmetry to Define Risk Factors for the Development of Complications in Twin… (NCT06782776) | Clinical Trial Compass
RecruitingNot Applicable
Role of Doppler Echoflowmetry to Define Risk Factors for the Development of Complications in Twin Pregnancies
Italy6,600 participantsStarted 2021-02-08
Plain-language summary
The goal of this observational study is to evaluate the outcomes of twin pregnancies referred to our center, in order to understand whether the use of different guidelines over time, with more systematic follow-up timing, has improved their management by reducing adverse events. All this would provide us with useful information for a better understanding of the effects of twinhood on pregnancy outcomes, so that we have more accurate information in counseling with patients.
Who can participate
Age range
18 Years – 44 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age \> 18 years
* Twin Pregnancy
* Ultrasound monitoring and delivery occurred at Policlinico S Orsola in Bologna, Italy
* Written informed consent form obtained from the patient
Exclusion Criteria:
* Completion of delivery at another facility
* Desire to undertake the Voluntary Interruption of Pregnancy
* Refusal to undergo instrumental monitoring and subsequent follow-up at our center
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Consequences of twinning on maternal and fetal hemodynamics
Timeframe: up to 100 weeks
Trial details
NCT IDNCT06782776
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna