Clinical Trials Directory

Trials / Unknown

UnknownNCT02865551

Urinary Retention After Vaginal Delivery With Epidural Anesthesia.

The Rate of Urinary Retention in Women After Vaginal Delivery With Epidural Anesthesia Who Underwent Prolonged Catheterization Compared With Intermittent Catheterization During Labor.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
160 (estimated)
Sponsor
Rambam Health Care Campus · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The investigators intend to compare the rate of urinary retention among female patients after vaginal delivery under epidural anesthesia, depending on bladder catheterization type, either by a foley catheter inserted adjacent to epidural anesthesia or intermittent catheterization applied every 4 hours during labor.

Detailed description

An explanation about the study will be delivered to each participant and each participant will sign a confirmed consent. Patients will be randomized between 2 groups of treatment: 1. intermittent catheterization applied every 4 hours during labor. 2. foley catheter inserted adjacent to epidural anesthesia. In patients with a foley catheter, the catheter will be removed soon after delivery. Participants will be followed by a clinician post labor. An abdominal US will be performed either 4 hours after delivery or after the participant urinates to check the bladder volume. Patient information including demographic information, information regarding the patient's pregnancy and delivery will be collected from the patient's electronic record.

Conditions

Interventions

TypeNameDescription
DEVICEFoley catheterExtended bladder catheterization after epidural anesthesia.
DEVICEShort term catheterIntermittent catheterization every 4 hours after epidural anesthesia.
DRUGEpidural anesthesiaPerformance of epidural anesthesia by a certified anesthesiologist.

Timeline

Start date
2019-07-01
Primary completion
2023-10-31
Completion
2023-12-31
First posted
2016-08-12
Last updated
2023-01-25

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT02865551. Inclusion in this directory is not an endorsement.