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Sentix: A prospective observational trial on sentinel lymph node biopsy in patients with early stage cervical cancer

Sentix: A prospective observational trial on sentinel lymph node biopsy in patients with early stage cervical cancer - Sentix

Status
Active, not recruiting
Phases
Phase 3
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48708
Enrollment
30
Registered
2017-09-18
Start date
2017-11-24
Completion date
Unknown
Last updated
2024-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervical cancer

Interventions

None listed

Sponsors

Central and Eastern European Gynecologic Oncology Group/ David Cibula
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Cervical cancer

Exclusion criteria

Exclusion criteria: Unable to understand protocol

Design outcomes

Primary

MeasureTime frame
Recurrence rate at the 24th month of follow-up

Secondary

MeasureTime frame
Prevalence of symptomatic pelvic lymphocele and lower extremity lymphedema, the two complications that are associated with lymph node staging.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)