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Duration of Stay After Urologic Surgery : Neuraxial Versus General Anesthesia

Duration of Stay for Outpatient Surgery After Tension Free Vaginal Tape (TVT) Urologic Surgery : Neuraxial Versus General Anesthesia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03517202
Enrollment
260
Registered
2018-05-07
Start date
2018-03-13
Completion date
2018-06-30
Last updated
2018-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary Retention

Keywords

Urologic surgery, Urinary incontinence, Tension Free Vaginal Tape, Post-operative urinary retention, Outpatient surgery

Brief summary

Outpatient midurethral surgery is a frequent surgery. It is performed either under general anesthesia or neuraxial anesthesia. A frequent complication is postoperative urinary retention requiring urinary catheterization, which implies a higher infectious risk. The investigators compared the complication rate after TVT surgery depending on the type of anesthesia.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * Sex: Female * Patient who has consented to the use of her medical data for research purposes. * Patient undergoing outpatient urinary incontinence surgery using TVT between 2012 and 2016

Exclusion criteria

* Specific clinical forms of the disease, * Interfering treatments and associated diseases, history, * Refusal of the patient to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
The investigators compared the rate of complications after TVT surgery depending on the type of anesthesia and the need for urinary catheterization, requiring longer hospital stay after surgery.The period from January 1st, 2012 to December 31st, 2016 will be examinedPatients hospitalized at Strasbourg University Hospital from 2012 to 2016.

Countries

France

Contacts

Primary ContactValentina FAITOT, MD
valentina.faitot@chru-strasbourg.fr03 88 12 70 75
Backup ContactGauthier VINEE, MD
gauthieremmanuel.vinee@chru-strasbourg.fr03 88 12 70 75

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026