Effect of Amnioinfusion on External Cephalic Version Successful Rate
AMNIO
1 other identifier
interventional
119
1 country
2
Brief Summary
The aim of the study is to evaluate the effect of transabdominal amnioinfusion before second external cephalic version after initial failure.Patient with a single foetus, at term, in breech presentation and after a first cephalic version are included. The randomisation determines whether the patient is included in the group with amnioinfusion before second cephalic version or with usual second cephalic version only; The efficacy's evaluation is based on rate of cephalic presentation at birth.Success rate of cephalic version with or without transabdominal amnioinfusion, rates of cesarian section in the two groups,maternal and fetal morbidity, time between second cephalic version and birth will be studied. Prospective interventional randomized sequential comparative multicentric study. A maximum of 240 patients will be included (120 in each group). As the study is sequential it will be over as soon as a significative difference is shown.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2006
Longer than P75 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2006
CompletedFirst Submitted
Initial submission to the registry
April 24, 2007
CompletedFirst Posted
Study publicly available on registry
April 25, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2011
CompletedDecember 30, 2025
December 1, 2025
4.8 years
April 24, 2007
December 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
cephalic presentation at birth
at birth
Study Arms (2)
A
EXPERIMENTALTransabdominal amnioinfusion performed before external cephalic version
V
NO INTERVENTIONWithout transabdominal amnioinfusion
Interventions
transabdominal amnioinfusion performed 4 to 24 hours before the second trial of external cephalic version
Eligibility Criteria
You may qualify if:
- single fetal pregnancy
- breech presentation
- at term
- initial failure of external cephalic version
- structurally normal foetus
You may not qualify if:
- polyhydramnios
- anhydramnios
- abnormality of the fetal heart rhythm
- uterine congenital malformation
- cesarian section for a previous birth
- unability to understand study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Mother Child University Hospital
Nantes, 44000, France
Olympe de Gouges Women Health Centre, Bretonneau University Hospital
Tours, 37000, France
Related Publications (42)
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BACKGROUNDRoyal College of Obstetricians and Gynaecologists The management of breech presentation. 2001
BACKGROUNDRoyal College of Obstetricians and Gynaecologists. Use of anti-D immunoglobulin for Rh Prophylaxis. London: RCOG Press; 1999. Guideline n° 22
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PMID: 11213120BACKGROUNDWagner A, Potin J, Himily V, Arbeille P, Perrotin F. The "Loss Of Resistance" Syringe: a useful tool for difficult amnioinfusion. Fetal Diagn Ther (submitted).
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PMID: 28279119RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Franck Perrotin, MD-PhD
Tours University Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 24, 2007
First Posted
April 25, 2007
Study Start
July 1, 2006
Primary Completion
May 1, 2011
Study Completion
May 1, 2011
Last Updated
December 30, 2025
Record last verified: 2025-12