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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02022553
Other study ID # NNKOR2013
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2006
Est. completion date December 2018

Study information

Verified date May 2024
Source Voronezh N.N. Burdenko State Medical Academy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

AIM OF RESEARCH. The aim of our research is to improve the results of the combined treatment of patients with locally advanced rectal cancer using endovascular methods and reservoir and plastic surgery. TASKS OF RESEARCH. 1. To assess the immediate and long-term results of combined (chemoradiation and surgical) treatment for locally advanced rectal cancer. 2. To make a comparative evaluation of the results of independent surgical and combined (chemoradiation and surgery) treatment of patients with locally advanced rectal cancer. 3. To examine functional results of surgical treatment with the formation of "neosphincter" and "neorectum" in patients with colorectal cancer.. 4. To study features of blood supply to the rectum from the pools of the inferior mesenteric and internal iliac arteries, using the method of selective angiography, in connection with the development of endovascular treatment of rectal cancer. 5. To develop and introduce into clinical practice method of one-stage selective intra-arterial oil chemoembolization of upper, middle and lower rectal arteries in patients with locally advanced rectal cancer, who have a contraindication to preoperative radiotherapy. 6. To assess the immediate and long-term results of combined (endovascular and surgical) treatment for locally advanced rectal cancer. 7. To optimize tactics of combined treatment of locally advanced rectal cancer by developing an algorithm of using chemoradiotherapy and endovascular interventions in the preoperative period. NOVELTY OF RESEARCH. 1. As a result of research will be designed and implemented a new method of selective intra-arterial chemoembolization in rectal arteries preoperatively in patients with locally advanced rectal cancer. 2. Substantiated high effectiveness of the proposed technique for the removal of colonic obstruction and, as a consequence perform radical surgical treatment of these patients. 3. First developed dosage and concentration of chemotherapeutic agent and embolic agent for safe injection when performing selective intra-arterial chemoembolization of rectal arteries. 4. Developed complex techniques of selective intra-arterial chemoembolization of rectal arteries preoperatively in patients with locally advanced rectal cancer. 5. Will be made a comparative analysis of the postoperative period and the evaluation of the quality of life of operated patients Obtained data will be presented for use in clinical practice. POSSIBLE APPLICATION AREAS. Results of the research designed for use in the treatment process of departments of Coloproctology, oncology, as well as the educational process of higher and secondary medical institutions. EXPECTED EFFECTIVENESS. It is expected that the use of this method of treatment of patients with locally advanced rectal cancer in clinical practice will provide pronounced effect: 1. Medical and social - improving the quality of care, preservation of social activity of patients, reducing mortality; 2. Economic - reducing the time of patients' treatment and reducing the number of therapeutic manipulation; 3. Science and Technology - improving of the training level of medicine workers in the treatment of patients with rectal cancer.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Clinical diagnosis of rectal cancer T3-4N0-2M0 - complication of bowel obstruction - No allergy on contrast agent - Previously not operated about rectal cancer - Not older than 75 years Exclusion Criteria: - Older 75 years - Previously operated about rectal cancer - Allergy to contrast agent - No bowel obstruction - No rectal cancer - No locally advanced rectal cancer - Clinical diagnosis of rectal cancer Tis-4N0-2M1 (generalized rectal cancer)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
usual rectal cancer surgery

RACHEL


Locations

Country Name City State
Russian Federation Voronezh Regional Hospital #1 Voronezh Voronezh Region

Sponsors (1)

Lead Sponsor Collaborator
Voronezh N.N. Burdenko State Medical Academy

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary tumor reduction 5-10 days