Clinical trial · Interventional
Pap Smear Collection With the Papette Brush
Pap Smear Collection With the Papette Brush: A Pragmatic Study
NCT05034614CI-TRIAL-00064345completedN/AResults postedClinicalTrials.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)
This research study is comparing Pap smear collection techniques using the Papette brush to traditional spatula and cytology brush for cervical cancer screening
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer Screening | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Papette brush collection | Diagnostic Test | — | UNRESOLVED |
| Spatula/cytology brush collection | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- OTHER
- label
- Pap smears using the Papette
- description
- Papette brush used to collect a Pap smear sample as standard of care.
- interventionNames
- Diagnostic Test: Papette brush collection
- type
- OTHER
- label
- Pap smears using the traditional spatula/cytology brush
- description
- Spatula/cytology brush used to collect a Pap smear sample as standard of care.
- interventionNames
- Diagnostic Test: Spatula/cytology brush collection
Primary outcomes (1)
- measure
- Specimen Adequacy
- timeFrame
- Baseline
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 21 Years
- Maximum age
- 64 Years
Show eligibility criteria text
Inclusion Criteria: * Adult women, aged 21-64 years old. * Have given consent for medical records to be accessed. * Who will have a Pap smear exam in CIM from July 2021 through June 2022. Exclusion Criteria: * Women, age \< 21 or \> 64. * Has vaginal spotting present during cervical sampling. * Did not give consent to have medical records accessed.
References
Publications (0)
Data not yet available
No reference posted for this study.