Uretal Flow Assessment During Gynecological Procedures

An Evaluation of Ureteral Flow After Temporary Bilateral Uterine Artery Occlusion During Conservative Gynecological Procedures

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00453882

Enrollment

Registered

2007-03-29

Start date

2006-11-30

Completion date

2007-04-30

Last updated

2012-01-30

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

Conditions

Conservative Gynecological Procedures

Brief summary

The objective is to evaluate the feasibility of using color Doppler ultrasound in ureteral flow assessment after uterine artery occlusion during a conservative gynecological procedure.

Interventions

DEVICEflostat (TM) System

Study design

Allocation

Intervention model

SINGLE_GROUP

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

25 Years to No maximum

Healthy volunteers

Inclusion criteria

* Meets criteria for conservative gynecological procedure * At least 25 years of age * Cervix suitable for tenaculum placement * Provides written informed consent.

Exclusion criteria

* Pregnancy * One or more lower uterine segment fibroids * Hydronephrosis as determined by renal ultrasound pre-procedurally * Clinical diagnosis of urinary tract infection (UTI) * In the medical judgment of the physician, such a procedure may compromise the patient's condition * Inability to achieve bilateral occlusion with the clamp placement during the procedure.

Design outcomes

Primary

Measure	Time frame
Ability to evaluate ureteric jets	—
Adverse events	—

Countries

United States

Outcome results

None listed

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