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NCT06147388: RECER
Regression of Cervical Precancerous Lesions and Associated Risk Factors
trial testing Colposcopy in Cervix Uteri SIL in 300 participants. Currently enrolling.
1 July 2026
Quick facts
| Lead sponsor | General University Hospital, Prague |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 300 |
| Start date | 1 September 2022 |
| Primary completion | 1 July 2026 |
| Estimated completion | 1 July 2027 |
| Sites | 1 location across Czechia |
Drugs / interventions tested
- Colposcopy
Conditions studied
- Cervix Uteri SIL — all drugs for Cervix Uteri SIL →
- HPV — all drugs for HPV →
- CIN2 — all drugs for CIN2 →
- CIN3 — all drugs for CIN3 →
Sponsor
General University Hospital, Prague
Who can join
Adults 18 to 40, female only, with Cervix Uteri SIL or HPV. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of this study is to assess the extent of histopathological regression of severe cervical precancerous lesions (CIN 2 and CIN 3); evaluate the proportion of patients who experience the normalization of HPV test and cytology finding among those who were treated conservatively and those who underwent conization; and identify predictive parameters associated with regression. Based on this analysis, a model will be proposed to predict the likelihood of lesion regression.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Regression of high-grade squamous intraepithelial cervical lesions and associated risk factors (RECER).
Dostalek L, Brynda D, Marek R, Hederlingova J, et al · · 2025 · PMID 40215795 · DOI 10.1016/j.ijgc.2025.101768
Verify or expand the search:
- PubMed search for NCT06147388
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Colposcopy
Trials testing the same drug.
- NCT07211204 — Comparison Of Cytology And Molecular Screening For Detecting Cervical Reactive Cellular Changes In General Population · NA · withdrawn
- NCT07281430 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S04) · 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 General University Hospital, Prague trials
Trials by the same sponsor.
- NCT07493928 — HPV After chemoRadioTherapy · recruiting
- NCT07495410 — Anderson-Fabry Disease Fitness Improvement Training: A-FAD-FIT · NA · enrolling by invitation
- NCT06942533 — Effect of Visual Feedback From the SpiroGym Mobile Application · NA · recruiting
- NCT06789978 — Rapid Prehospital ACcess to ECPR in Prague · NA · recruiting
- NCT06585332 — Handgrip and Respiratory Dysfunction in HD Patients. · completed
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 NCT06147388 (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 General University Hospital, Prague
- Last refreshed: 25 February 2026
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/NCT06147388.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing