High-Resolution Anoscopy Perceived Discomfort Study

Completed · Not applicable

Conditions studied: Pain, Anal Cancer

In brief

Study should determine if performing the less uncomfortable part of the exam (the perianal exam) results in less recalled discomfort if performed last vs. if performed first.

Key facts

Study ID

NCT04083053

Run by

Wake Forest University Health Sciences

People needed

54

Starts

2019-09-17

Expected to finish

2021-01-15

Last updated by the study team

2021-01-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Present for a previously scheduled high resolution anoscopy procedure
• Able to participate in an English written survey following the HRA procedure

You may not qualify if…

• Undergoing ablation during the HRA procedure
• Inability to tolerate or complete the HRA procedure
• Unwillingness or inability to complete the post-procedure survey
• Previous participation in the study

Where it is running

• Wake Forest University School of Medicine — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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