Medium and Long-term Complications of the Patients Having Had a Vaginal Caesarian in Hospital René Dubos
NCT ID: NCT03052699
Last Updated: 2017-02-14
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.
COMPLETED
26 participants
OBSERVATIONAL
2015-09-30
2015-11-30
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.
Vaginal Birth After Caesarean Section and Levator Ani Avulsion
NCT03420001
Role of the Intrapartum Grobman Nomogram in the Indication of Attempted Vaginal Delivery After Cesarean Section
NCT06202768
Parents' Expectations and Experiences Around Cesarean Section in Belgium
NCT02609217
Exploring Taiwanese Womens' Decision-making Regarding Vaginal Birth After Caesarean Section
NCT01210300
Additional Effect of Wound Infiltration After Cesarean Section With Optimal Standard Analgesia
NCT01751256
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
It has several advantages: simplicity of the technique, the dissection of tissues is limited, low risk of bleeding and no abdominal scar.
The purpose is to determine the risk factors of the maternal morbi-mortality and to estimate the long-term results
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.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
vaginal Cesarean Section
patients operated to vaginal Cesarean Section
vaginal Cesarean Section
follow-up to patients operated for vaginal Cesarean Section
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
vaginal Cesarean Section
follow-up to patients operated for vaginal Cesarean Section
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.
Hôpital NOVO
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
MARKOU Georges, PH
Role: PRINCIPAL_INVESTIGATOR
Rene Dubos Hospital
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CHRD1115
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.