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KOrean Borderline Ovarian Tumor (KOBOT) Registry

Establishing the Registry of Korean Patients With Borderline Ovarian Tumors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02803970
Acronym
KOBOT
Enrollment
3000
Registered
2016-06-17
Start date
1994-12-31
Completion date
2040-12-31
Last updated
2019-04-03

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

Conditions

Ovarian Neoplasms

Brief summary

The aim of this study is to collect data on Korean patients with borderline ovarian tumors.

Detailed description

The researchers retrospectively collected data on Korean patients with borderline ovarian tumors (BOTs) diagnosed, treated, and followed between November 1994 and February 2015 at institutions where placed in the Republic of Korea. And the researchers prospectively will collect data on all Korean patients with BOTs at institutions where placed in the Republic of Korea since March, 2015. If patients agree to participate in this KOBOT registry, patient's data (such as age, body mass index, preoperative findings, laboratory findings, radiologic findings, operative findings, pathologic findings, postoperative findings) will be collected in a research database. The research database will be updated, every 6 month, to include data on patient's disease outcome and follow-up care. Although most data will be collected form the medical record, patient may agin be contacted so that researchers can collection some data if it is not in the medical record.

Interventions

None listed

Sponsors

Kangbuk Samsung Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Patients with borderline ovarian tumors (BOTs) diagnosed, treated, and followed between November 1994 and February 2015 at institutions where placed in the Republic of Korea. * All patients undergoing gynecologic surgery for BOTs at institutions where placed in the Republic of Korea since March, 2015

Exclusion criteria

* Patients who did not receive primary treatment or follow-up for at least 6 months at each institution were excluded from analysis

Design outcomes

Primary

MeasureTime frame
Recurrence-free survivalup to 100 months

Countries

South Korea

Contacts

Primary ContactTaejong Song, MD,PhD
taejong.song@gmail.com82-2-2001-2582

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026