Clinical trial · Interventional
High-Resolution Anoscopy Perceived Discomfort Study
NCT04083053CI-TRIAL-00049695completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Anal Cancer | Malignant Anal Neoplasm | CURATED_EXACT | 0.92 |
| Pain | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| high-resolution anoscopy (HRA) with biopsy | Procedure | — | UNRESOLVED |
| Perianal Exam | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Perianal Exam First
- description
- Perianal exam that is a part of anal cancer screening will be performed prior to the intraanal portion of the exam (high-resolution anoscopy with biopsy).
- interventionNames
- Procedure: Perianal Exam
- Procedure: high-resolution anoscopy (HRA) with biopsy
- type
- EXPERIMENTAL
- label
- Perianal Exam Last
- description
- Perianal exam that is a part of anal cancer screening will be performed after the intraanal portion of the exam (high-resolution anoscopy with biopsy).
- interventionNames
- Procedure: Perianal Exam
- Procedure: high-resolution anoscopy (HRA) with biopsy
Primary outcomes (1)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Present for a previously scheduled high resolution anoscopy procedure * Able to participate in an English written survey following the HRA procedure Exclusion Criteria: * 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
References
Publications (0)
Data not yet available
No reference posted for this study.