Impact of Ureteral Stent and Sheaths Size on Post-Operative Pain

Overview

About this study

The purpose of this study is to determine if post-operative stent size impacts stent-related pain and discomfort. 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

​​​​​​​Inclusion Criteria:

  • Aged 18 years and over.
  • Patients undergoing a retrograde intra-renal surgery (RIRS) (only patients undergoing the procedure for stone treatment will be included) who will require post-operative indwelling ureteral stent placement on a string at the conclusion of the procedure.
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Exclusion Criteria:

  • Patients with intra-operative ureteral injury who will require ureteral stent for extended time (more than 10 days, in that case a stent without a string will be used).
  • Patient undergoing ureteroscopy for any indication other than stone extraction.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 08/19/2024. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Meghan Cooper, D.O.

Contact us for the latest status

Contact information:

Kathryn Barthels

(507) 538-5772

Barthels.Kathryn@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20581034

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