Curative Chemoradiation of Low Rectal Cancer

NCT ID: NCT02438839

Last Updated: 2026-01-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

108 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-09-30

Study Completion Date

2026-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of the present study is to investigate whether curative chemoradiation of low rectal cancer is feasible, safe and effective in a multicenter study with results comparable to those of single center studies.

Results from previous studies indicate that a considerable fraction of patients with low rectal cancer can be cured by a combination of radiation and chemotherapy alone and thus be spared from operation.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Rectal Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Histopathologically verified adenocarcinoma of the rectum
* Planned abdominoperineal resection (APR) or ultralow resection
* Primary, resectable T1-T3, N0 tumor. N1 nodal disease is acceptable, if the positive lymph nodes are localized to the mesorectum at the level of the tumor.
* Distance from anal verge to lower edge of tumor ≤ 6 cm measured by rigid rectoscope
* Performance status 0-2
* Patient acceptance to collection of biopsies and blood samples for translational research
* Age ≥ 18 years
* Normal function of bone marrow as evaluated by

* neutrophils ≥ 1.5 x 10\^9/l
* thrombocytes ≥ 100
* Normal function of liver

* alanine aminotransferase (ALAT) \< 2.5 x upper limit of normal
* bilirubin \< 2.5 x upper limit of normal
* Kidney function

\- Serum creatinine \< 1.5 x upper limit of normal or measured glomerular filtration rate (GFR) \> 30 ml/min
* Fertile women must present a negative pregnancy test and use secure contraceptives during and 3 months after treatment.
* Written and orally informed consent

Exclusion Criteria

* Previous surgical treatment of the present cancer, including transanal excision of tumor.
* Other malignant disease within the past five years except basocellular skin cancer and carcinoma in situ cervicis uteri
* Distant metastases verified by imaging or biopsy
* Previous radiation treatment of the pelvis
* Pregnant or breastfeeding women
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Vejle Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Anders Jakobsen, DMSc

Role: STUDY_CHAIR

Department of Oncology, Vejle Hospital

Henrik Jensen, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Oncology, Vejle Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Oncology, Aalborg University Hospital

Aalborg, , Denmark

Site Status

Department of Surgery, Aalborg University Hospital

Aalborg, , Denmark

Site Status

Department of Oncology, Rigshospitalet

Copenhagen, , Denmark

Site Status

Department of Oncology, Vejle Hospital

Vejle, , Denmark

Site Status

Department of Surgery, Vejle Hospital

Vejle, , Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

WW2

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Anal Cancer Radiotherapy Study
NCT01937780 ACTIVE_NOT_RECRUITING