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Pain Management for Cystoscopy: A Prospective Randomized Study Focused on Understanding the Role of the Bag Squeeze to Manage Pain for Patients Undergoing Cystoscopy

Pain Management for Cystoscopy: A Prospective Randomized Study Focused on Understanding the Role of the Bag Squeeze to Manage Pain for Patients Undergoing Cystoscopy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04198064
Acronym
PMC
Enrollment
201
Registered
2019-12-13
Start date
2019-09-16
Completion date
2019-11-12
Last updated
2019-12-13

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

Conditions

Pain, Procedural

Brief summary

The purpose of this study is to determine whether utilization of the bag squeeze technique during flexible cystoscopy changes pain scores using a study questionnaire designed by the team which comprises a validated Lingard pain rating scale.

Interventions

PROCEDUREBag Squeeze

Participants will receive a bag squeeze of irrigation fluid (500 ml/\ 2 cups of % 0.9 saline solution) during the insertion of the cystocopy tube during their cystocopy.

PROCEDURENo Bag Squeeze

Participants will receive a standard cystocopy procedure as per standard of care.

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Male * Undergoing flexible cystocopy at University Health Network that have undergone a flexible cystocopy and did not demonstrate difficulty during exploration (meatal stenosis or urethral stricture), simultaneous removal or ureteral stents or bladder biopsies or have a chronic history of pelvic pain

Exclusion criteria

\- Patients that do not meet the inclusion criteria.

Design outcomes

Primary

MeasureTime frameDescription
Pain RatingThe outcome measure will be assessed for up to 4 hours after consent and completion of clinical procedure.Participants will be asked to rate their pain on the study-specific Lingard pain scale post-cystocopy. The Lingard pain scale is an outcome measure scaled from 0 (no pain) to 10 (pain as bad it could be). The higher the reported rating out of 10, the more pain the participant has experienced.

Countries

Canada

Outcome results

None listed

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