Procedure RACHEL in Complex Treatment of Rectal Cancer
RACHEL
Complex Treatment of Rectal Cancer
1 other identifier
interventional
52
1 country
1
Brief 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.
- 8.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.
- 9.Substantiated high effectiveness of the proposed technique for the removal of colonic obstruction and, as a consequence perform radical surgical treatment of these patients.
- 10.First developed dosage and concentration of chemotherapeutic agent and embolic agent for safe injection when performing selective intra-arterial chemoembolization of rectal arteries.
- 11.Developed complex techniques of selective intra-arterial chemoembolization of rectal arteries preoperatively in patients with locally advanced rectal cancer.
- 12.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.
- 13.Medical and social - improving the quality of care, preservation of social activity of patients, reducing mortality;
- 14.Economic - reducing the time of patients' treatment and reducing the number of therapeutic manipulation;
- 15.Science and Technology - improving of the training level of medicine workers in the treatment of patients with rectal cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2006
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2006
CompletedFirst Submitted
Initial submission to the registry
December 19, 2013
CompletedFirst Posted
Study publicly available on registry
December 30, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2018
CompletedMay 6, 2024
May 1, 2024
12.8 years
December 19, 2013
May 2, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
tumor reduction
5-10 days
Study Arms (2)
rectal cancer, surgery
EXPERIMENTALrectal cancer, RACHEL, surgery
ACTIVE COMPARATORInterventions
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Voronezh Regional Hospital #1
Voronezh, Voronezh Oblast, 394066, Russia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- M.D.
Study Record Dates
First Submitted
December 19, 2013
First Posted
December 30, 2013
Study Start
February 1, 2006
Primary Completion
December 1, 2018
Study Completion
December 1, 2018
Last Updated
May 6, 2024
Record last verified: 2024-05