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NCT05210348: Urine-hrHPV
Clinical Evaluation of Detection of High Risk HPV in Urine
trial in Human Papillomavirus Infection in 1,000 participants. Status unknown.
1 February 2022
Quick facts
| Lead sponsor | Peking University People's Hospital |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 1,000 |
| Start date | 15 September 2021 |
| Primary completion | 1 February 2022 |
| Estimated completion | 1 May 2022 |
| Sites | 3 locations across China |
Conditions studied
- Human Papillomavirus Infection — all drugs for Human Papillomavirus Infection →
- Cervical Cancer — all drugs for Cervical Cancer →
- Human Papilloma Virus — all drugs for Human Papilloma Virus →
- Negative for Intraepithelial Lesion or Malignancy — all drugs for Negative for Intraepithelial Lesion or Malignancy →
Sponsor
Peking University People's Hospital
Who can join
Adults 20 to 65, female only, with Human Papillomavirus Infection or Cervical Cancer. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Cervical cancer is one of the most common tumors in women, which seriously threatens women's life quality and safety. Human papilloma virus (HPV) infection is the most common cause of cervical cancer. Traditional HPV testing is based on the cells sample shed from the cervix. Recent studies have shown that urine HPV detection can be used as a new HPV detection method. This study intends to include patients undergoing TCT /HPV test/colposcopy in the department of gynecological diseases of the hospital, and collect urine samples and cervical swab samples. Sanger sequencing and cervical swab HPV test results were compared to evaluate the accuracy and clinical validity of urine HPV test combined with clinical diagnosis results of cases.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Clinical Performance of a Dedicated Urine-Based Assay for the Detection of Human Papillomavirus and Cervical Intraepithelial Neoplasia.
Zhao Y, Zhao L, Wang Z, Cui S, et al · · 2023 · cited 3× · PMID 38077232 · DOI 10.2147/ijwh.s424621
Verify or expand the search:
- PubMed search for NCT05210348
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Human Papillomavirus Infection
Currently open trials in the same condition.
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- NCT06598475 — Investigating Facilitator-driven, Multi-level Implementation Strategies in Federally Qualified Health Centers to Improve · NA · recruiting
- NCT06611553 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S02) · NA · active not recruiting
- NCT06611540 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S03) · NA · active not recruiting
- NCT06498661 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S01) · NA · recruiting
Other Peking University People's Hospital trials
Trials by the same sponsor.
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- NCT07500441 — Digital PCR of CHIP and MR for MRD Monitoring After Allo-HSCT in AML · recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05210348 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Peking University People's Hospital
- Last refreshed: 27 January 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05210348.
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