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RecruitingNCT07112937Updated Nov 10, 2026

The Effect of Multimodal Treatment of Rectal Cancer on Circulating Tumor Cells: A Prospective, Observational Study

An observational study in Rectal Cancer Patients, sponsored by The Institute of Molecular and Translational Medicine, Czech Republic. Recruiting at 1 site in Czechia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by The Institute of Molecular and Translational Medicine, Czech Republic · Observational

From the registry’s dates

  • Started May 2023; still recruiting 3 years 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study summary

The prospective study will focus on patients undergoing multimodal treatment for rectal cancer. The main objective of the study will be to monitor changes in circulating tumor cells (CTCs) in the peripheral blood of patients during multimodal treatment. For each patient enrolled in the study, peripheral blood samples will be collected at specified time intervals to determine the presence and quantity of CTCs.

The CTCs levels will be compared among rectal cancer patients with neoadjuvant chemoradiotherapy and without neoadjuvant chemotherapy.

02

Conditions studied

  • Rectal Cancer Patients

Keywords

  • circulating tumor cells
03

In context

Neoplastic Cells, Circulating

227 studies on the registry are indexed under Neoplastic Cells, Circulating; 54 are open to participants now.

This study's planned enrollment of 150 is above the median of 120 across 121 observational studies indexed under Neoplastic Cells, Circulating.

Browse Neoplastic Cells, Circulating studies →

Lead sponsor

The Institute of Molecular and Translational Medicine, Czech Republic is the lead sponsor of 18 studies on the registry; 10 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
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Rectal cancer patients

Eligibility criteria

Inclusion Criteria: rectal cancer -

Exclusion Criteria: no other cancer

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Rectal cancer patients with neoadjuvant chemoradiotherapy
  • Rectal cancer patients without neoadjuvant chemoradiotherapy
06

What researchers measure

Primary outcomes

  1. Levels of circulating tumor cells in peripheral blood

    The levels of circulating tumor cells will be measured in rectal cancer patients

    Time frame: The levels of circulating tumor cells will be measured in 5 time points: before neoadjuvant chemoradiotherapy, in 3. week of chemoradioterapy, before surgery, one week after surgery and one month after surgery.

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Ihnat P, Srovnal J, Hrubovcak J, Martinek L. Detection and clinical significance of circulating tumour cells in patients with colorectal carcinoma. Rozhl Chir. 2023;102(10):376-380. doi: 10.33699/PIS.2023.102.10.376-380. PubMed 38302423 ↗

Individual participant data

Plan to share: Yes — Patients code; sex; age; diagnosis; clinical, laboratory and experimental findings

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started May 2023 (actual). Primary completion is estimated for Dec 2026, 43 months after the start.

Of 59 observational studies under Neoplastic Cells, Circulating, half reached primary completion within 93 months of starting (the median), counting those still running; a quarter within 38. This study's planned 43 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 1, 2025
First posted
Aug 8, 2025
StartActual
May 2, 2023
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2027
Last update
Nov 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
1 update, last Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07112937
Lead sponsor
The Institute of Molecular and Translational Medicine, Czech Republic
Responsible party
Sponsor
First posted
Aug 8, 2025
Start date
May 2, 2023
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Nov 10, 2026

Study contacts

Josef Srovnal, Associate professor, MD, PhD
Contact
josef.srovnal@upol.cz
+420 585632137

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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