Evaluation of the Absence of Intraoperative Bladder Catheterization in Case of Planned Cesarean Section
Recruiting
N/A
Interventional Study
Pregnant Women
Cesarean Section
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 550 (estimated)
- Sponsor
- University Hospital, Montpellier · Other
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About This Trial
The hypothesis of this trial is that the absence of systematic bladder catheterization in patients performing spontaneous urination in the hour preceding the planned cesarean section under spinal anesthesia would not lead to more bladder heterocatheterization for postpartum urinary retention (RUPP) in the 24 hours post-cesarean section than systematic intraoperative bladder catheterization up to 2…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult patient
* Patient admitted for a planned cesarean section after 34 weeks under spinal anesthesia
* Single or twin pregnancy
* Unscarred or with one or two scars of the uterus
Exclusion Criteria:
* Positive urine test strip showing a presence of nitrites or leukocytes, …
Contacts