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Not yet recruitingNCT07153705Updated Sep 4, 2025

OCS Products Based on Exosome Technology Were Applied in the Recurrence Monitoring Study After the Initial Treatment of Baseline CA125-negative Ovarian Cancer

An observational study in Ovarian Cancer, sponsored by Beihua Kong. Not yet recruiting. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-09-04.

Sponsored by Beihua Kong · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
32
Ages
18 Years and older
Sex
Female
01

Study summary

To study the performance of OCS products based on exosome detection technology in monitoring the recurrence of baseline CA125-negative ovarian cancer patients after initial treatment, and to explore reliable methods for monitoring the recurrence of baseline CA125-negative ovarian cancer patients after initial treatment.

02

Conditions studied

  • Ovarian Cancer

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03

In context

Ovarian Neoplasms

2,695 studies on the registry are indexed under Ovarian Neoplasms; 727 are open to participants now.

This study's planned enrollment of 32 is below the median of 200 across 527 observational studies indexed under Ovarian Neoplasms.

Browse Ovarian Neoplasms studies →

Lead sponsor

Beihua Kong is the lead sponsor of 3 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with ovarian cancer

Inclusion criteria

  1. Women over 18 years old;
  2. Pathologically confirmed as stage I-IV primary epithelial ovarian malignant tumor;
  3. ECOG \< 2;
  4. The expected survival period exceeds 6 months;
  5. CA125 ≤ 35 U/ml before initial treatment;
  6. Undergo surgery and adjuvant chemotherapy;
  7. The period between diagnosis and enrollment does not exceed 8 weeks;
  8. Be willing to provide blood samples for OCS testing during the research process;
  9. Sign the informed consent form.

Exclusion criteria

Exclusion criteria

  1. Have had other malignant tumors within the last five years;
  2. Have received any treatment for ovarian cancer;
  3. Benign ovarian mass;
  4. Non-primary ovarian tumors;
  5. Combined with other malignant tumors;
  6. Patients receiving neoadjuvant therapy;
  7. Pregnancy.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
32 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. OCS product inspection

    Time frame: Before the operation

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07153705
Lead sponsor
Beihua Kong
Responsible party
Beihua Kong (archiater, Shandong University) — Sponsor-investigator
First posted
Sep 4, 2025
Start date
Sep 1, 2025 (estimated)
Primary completion
Apr 1, 2026 (estimated)
Completion
Apr 1, 2026 (estimated)
Last update
Sep 4, 2025
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

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