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Evaluating ureteral patency in the post-indigo carmine era: a randomized controlled trial
Cara L Grimes1, Sonali Patankar1, Timothy Ryntz1
1Department of Obstetrics and Gynecology, Columbia University Medical Center, New York, NY.
Mannitol bladder distention during cystoscopy offers the highest surgeon satisfaction for evaluating ureteral patency. This method provides superior visualization and ease of use without increasing surgery or cystoscopy times.
Area of Science:
- Urology
- Gynecologic Surgery
- Pelvic Reconstructive Surgery
Background:
- Accurate intraoperative evaluation of ureteral patency is critical for gynecologic, urologic, and pelvic reconstructive surgeries.
- Several methods exist for assessing ureteral patency during cystoscopy.
Purpose of the Study:
- To compare surgeon satisfaction with four methods of evaluating ureteral patency during cystoscopy.
- Methods compared: oral phenazopyridine, intravenous sodium fluorescein, mannitol bladder distention, and normal saline bladder distention.
Main Methods:
- An unblinded randomized controlled trial was conducted.
- 130 subjects were randomized to one of the four methods.
- Surgeon satisfaction was the primary outcome, measured by a visual analog scale (VAS).
- Secondary outcomes included ease of use, visualization quality, and time to confidence in ureteral jet visualization.
Main Results:
- Mannitol bladder distention resulted in the highest surgeon satisfaction (median VAS 0 mm) compared to phenazopyridine (48 mm), sodium fluorescein (20 mm), and normal saline (23 mm) (P < .001).
- No significant differences were observed in surgery length, cystoscopy length, or time to surgeon confidence across the groups.
- No differences in adverse events, including urinary tract infections, were reported during the 189-day follow-up.
Conclusions:
- Mannitol bladder distention is the most satisfactory method for assessing ureteral patency during cystoscopy.
- It offers improved ease of use and visualization without negatively impacting procedure times.
- The method is safe, with no increase in adverse events observed.
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