External Cephalic Version (ECV) for Twins With Non-vertex Presenting Twin
NCT ID: NCT05894785
Last Updated: 2024-04-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
30 participants
INTERVENTIONAL
2022-02-27
2025-12-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Twin A Breech External Cephalic Version Intervention Trial (TWEXIT)
NCT04579835
The Difference Between Elasticity of the Uterine Cervix in Singleton and Twin Pregnancies
NCT02283567
Short Cervix - Twins
NCT03022591
Transperineal Ultrasound for the Female Pelvic Floor in Women With Multiple Gestation
NCT00790504
Fetal Reduction: Mechanical vs Chemical
NCT03473158
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Study group
External cephalic version
An ECV attempt is made on the study group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
External cephalic version
An ECV attempt is made on the study group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Shaare Zedek Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Zvi Ehrlich
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Shaare Zedek Medical Center
Jerusalem, , Israel
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Zvi Ehrlich, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
0327-21-SZMC
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.