Clinical trial · Interventional
Primary HPV Self-Collection in Indonesia
HPV DNA Screening With Self-Collection Method and Its Management in the Context of Population-Based Cervical Cancer Screening Pilot Project in Indonesia
NCT06942286CI-TRIAL-00095265enrolling by invitationN/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)
The purpose of this study is to implement human papillomavirus (HPV) self-collection in Indonesia.
Conditions
Conditions (3)
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 Cancers | Malignant Cervical Neoplasm | CURATED_EXACT | 0.92 |
| CIN - Cervical Intraepithelial Neoplasia | — | UNRESOLVED | — |
| Human Papillomavirus (HPV) | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| HPV Self-Collection | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- HPV Self-Collection
- description
- Participants will perform HPV self-collection.
- interventionNames
- Diagnostic Test: HPV Self-Collection
Primary outcomes (1)
- measure
- Success Rate of HPV Self-Collection
- timeFrame
- from enrollment to receipt of results, up to 8 weeks
- description
- number of subjects with valid HPV test results from self-collection / number of eligible subjects
Secondary outcomes (6)
- measure
- HPV Self-Collection Invitation Coverage
- timeFrame
- from enrollment to receipt of results, up to 8 weeks
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 30 Years
- Maximum age
- 69 Years
Show eligibility criteria text
Inclusion Criteria: * Age 30-69 years old * Have not had a Pap test within the last 3 years or an HPV test within the last 5 years * Have never been diagnosed with cervical cancer or high-grade dysplasia * Have no history of hysterectomy with cervical removal * Expressed willingness to participate in the study, including conducting HPV self-collection, follow-up treatment, and related surveys Exclusion Criteria: * Being pregnant or within 6 weeks postpartum * Women who have never engaged in sexual activity * Medical, psychiatric, or other conditions that may interfere with compliance with protocols, security assessments, and/or ability/competence to give informed consent * Adults who do not have the capacity to give consent may be excluded, as participants must be able to perform activities required by the protocol
References
Publications (0)
Data not yet available
No reference posted for this study.