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NCT04083053 · ClinicalTrials.gov registry record · NA
High-Resolution Anoscopy Perceived Discomfort Study
A NA study, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 54
- Enrollment target
NCT04083053 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 54 participants.
The verdict
NCT04083053, a NA study, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 54 participants
- Enrollment target
Study Summary
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.
Interventions
- PROCEDURE Perianal Exam
- PROCEDURE high-resolution anoscopy (HRA) with biopsy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 54 participants |
| Start Date | 2019-09-17 |
| Est. Completion | 2021-01-15 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04083053
The ClinicalTrials.gov registry entry for NCT04083053 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Perianal Exam is the first listed.
NCT04083053 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04083053 about?
NCT04083053 is a clinical study titled "High-Resolution Anoscopy Perceived Discomfort Study". 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.
What is the current status of trial NCT04083053?
This trial is currently completed. It is a NA study. The enrollment target is 54 participants. The study started on 2019-09-17. Estimated completion is 2021-01-15.
What interventions are being tested in trial NCT04083053?
The interventions under investigation include: Perianal Exam (PROCEDURE), high-resolution anoscopy (HRA) with biopsy (PROCEDURE).
Who is sponsoring clinical trial NCT04083053?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
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