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Self-expandable Metal Stent (SEMS) Endoscopic Placement for Malignant Colonic Obstruction Therapy (PATENCY)

Primary Purpose

Neoplasms,Colorectal

Status
Recruiting
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Stoma formation
Endoscopic self-expandable metal stent placement
Sponsored by
Russian Society of Colorectal Surgeons
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neoplasms,Colorectal

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients are 18 years old or older Stage I-IV according to TNM classification Patients with malignant colonic obstruction Overall health status according to ASA classification: I-III Overall health status according to Charlson comorbidity index ≤ 8 points Signed informed consent with agreement to attend all study visits The patient is not pregnant Exclusion Criteria: Inflammatory bowel disease Acute purulent process in the abdominal cavity The patient wants to withdraw from the clinical trial Loss to follow-up

Sites / Locations

  • Clinic of colorectal and minimally invasive surgery University Hospital n2, Clinical Center Sechenov First Moscow State Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Self-expandable metal stent (SEMS) endoscopic placement.

Stoma formation.

Arm Description

Anesthesia will include only propofol injection. A covered or partially covered metal self- expanding stent is placed in the area of tumor stenosis by the conductor, symmetrically in relation to the area of tumor stenosis.

Anesthetic care will include general endotracheal anesthesia with positioning of nasogastric tube and bladder catheterization. The diverting stoma formation will be proceed in 10 sm proximally to tumor.

Outcomes

Primary Outcome Measures

Bowel preparation (absence of feaces) according to Boston Bowel Preparation Scale
Evaluated via colonoscopy in colon and rectum distal to the tumour. Total score of bowel preparation measured from 0 to 9. The maximum BBPS score for a perfectly clean colon without any residual liquid is 9 and the minimum BBPS score for an unprepared colon is 0. This is evaluated by the endoscopist

Secondary Outcome Measures

Intraoperative complications rate during stoma formation or stent placement
The rate of complications during the procedure
Early postoperative complications rate after stoma formation or stent placement
The rate of complications after the procedure
Length of hospital stay after stoma formation or stent placement
Number of days spent in hospital after procedure
Quality of life before and after stoma formation or stent placement
Measured by patient-reported SF-36 scale before and after procedure
Operation time of resectional surgery
The duration of surgical procedure in minutes
Stoma formation rate
The percentage of patients who had preventive or definitive stoma during resectional surgery in the SEMS group
Stoma reversal rate
The rate of previously formed stoma reversal simultaneously with tumor resection
Early postoperative complications rate after resectional surgery
The rate complications after tumor resection surgery
Length of hospital stay after resectional surgery
Number of days spent in hospital after tumor resection surgery
Intraoperative complications rate during resectional surgery
The rate of complications during tumor resection surgery
Late complications rate during resectional surgery
The rate of complications after tumor resection surgery

Full Information

First Posted
June 10, 2022
Last Updated
December 1, 2022
Sponsor
Russian Society of Colorectal Surgeons
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1. Study Identification

Unique Protocol Identification Number
NCT05643989
Brief Title
Self-expandable Metal Stent (SEMS) Endoscopic Placement for Malignant Colonic Obstruction Therapy
Acronym
PATENCY
Official Title
Randomized Non-inferiority Single-center Prospective Trial of Malignant Colonic Obstruction Therapy With Self-expandable Metal Stent (SEMS) Endoscopic Placement or Stoma Formation.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
February 1, 2023 (Anticipated)
Study Completion Date
May 11, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Russian Society of Colorectal Surgeons

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Compare the effectiveness of Self-expandable metal stent (SEMS) and diverting stoma formation for the bowel preparation as a bridge to surgical treatment of patients with MCO.
Detailed Description
Surgical treatment of MCO is associated with high mortality and frequent development of postoperative complications. Stoma formation is the traditional method of urgent treatment of MCO. Currently there are more than 150 methods of colorectal stomas formation, but all of themare associated with a high risk of complications (10-20%), inclusively both early and late postoperative period. It results in longerhospital stay and requires additional financial expenses, also reoperations can be fatal for patients. Analysis of recent publications devoted to the treatment of MCO shows increasing implemented of new strategies of patents management, such as "fast track surgery", or "fast track recovery strategy" in clinical practice. Minimally invasive endoscopic procedures as a first stage of MCO treatment leads to transformation of previously performed multi-stage surgical interventions into one - stage. Development of up-to-date endoscopic science and technology provides a wide usage ofself-expandable metal stent (SEMS) in clinical practice. This strategy helps to avoid stoma formation or emergency surgery, becoming a "bridge" to a radical surgery. There are currently no studies directly comparing discharge stoma with endoscopic self-expandable metal stenting in preparation for colorectal cancer radical surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasms,Colorectal

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
56 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Self-expandable metal stent (SEMS) endoscopic placement.
Arm Type
Active Comparator
Arm Description
Anesthesia will include only propofol injection. A covered or partially covered metal self- expanding stent is placed in the area of tumor stenosis by the conductor, symmetrically in relation to the area of tumor stenosis.
Arm Title
Stoma formation.
Arm Type
Placebo Comparator
Arm Description
Anesthetic care will include general endotracheal anesthesia with positioning of nasogastric tube and bladder catheterization. The diverting stoma formation will be proceed in 10 sm proximally to tumor.
Intervention Type
Procedure
Intervention Name(s)
Stoma formation
Intervention Description
Trocar placement: the optical trocar (10 mm) will be inserted just near umbilicus . An abdominal revision is performed to determine the location of the tumor. Colon in 10 sm proximally to tumor is prepared for the discharge stoma formation. In the corresponding location on the anterior abdominal wall is formed incision of skin and subcutaneous tissue to the aponeurosis, the cut length is 2.5 sm. After that, aponeurosis crucial incision is performed. The previously prepared colon is brought out to the anterior abdominal wall with the help of a grasper. Discharge stoma is attached to a holding device; colon is fixed by the interrupted sutures (Polysorb 3-0). In the operating room, the stoma is opened, the intestinal patency is checked in both directions, and hemostasis is revealed. With the help of optics, the presence of intestinal tension is checked; if necessary, the colon is additionally mobilized.
Intervention Type
Procedure
Intervention Name(s)
Endoscopic self-expandable metal stent placement
Intervention Description
The colonoscope is passed to the distal edge of the tumor and a biopsy of the tumor is performed (if the tumor has not previously been verified). Through the tumor stenosis radioscopically guided metal conductor with atraumatic distal end installs in the proximal colon. A covered or partially covered metal self- expanding stent is placed in the area of tumor stenosis by the conductor, symmetrically in relation to the area of tumor stenosis. Radioscopically and endoscopically guided disclosure of a SEMS is performed immediately after which there is an abundant discharge of gases and intestinal contents. Upon completion of the procedure, the patient is transferred to the patient's room. The next day, a control X-ray of the abdomen is taken.
Primary Outcome Measure Information:
Title
Bowel preparation (absence of feaces) according to Boston Bowel Preparation Scale
Description
Evaluated via colonoscopy in colon and rectum distal to the tumour. Total score of bowel preparation measured from 0 to 9. The maximum BBPS score for a perfectly clean colon without any residual liquid is 9 and the minimum BBPS score for an unprepared colon is 0. This is evaluated by the endoscopist
Time Frame
on the 3rd day after obstruction treatment (SEMS or stoma formation)
Secondary Outcome Measure Information:
Title
Intraoperative complications rate during stoma formation or stent placement
Description
The rate of complications during the procedure
Time Frame
1 day (the day of procedure)
Title
Early postoperative complications rate after stoma formation or stent placement
Description
The rate of complications after the procedure
Time Frame
up to 7 days after procedure
Title
Length of hospital stay after stoma formation or stent placement
Description
Number of days spent in hospital after procedure
Time Frame
30 days after procedure
Title
Quality of life before and after stoma formation or stent placement
Description
Measured by patient-reported SF-36 scale before and after procedure
Time Frame
-1 day (before procedure), 3rd and 7th day after procedure
Title
Operation time of resectional surgery
Description
The duration of surgical procedure in minutes
Time Frame
1 day (the day of tumor resection surgery )
Title
Stoma formation rate
Description
The percentage of patients who had preventive or definitive stoma during resectional surgery in the SEMS group
Time Frame
1 day (the day of tumor resection surgery )
Title
Stoma reversal rate
Description
The rate of previously formed stoma reversal simultaneously with tumor resection
Time Frame
1 day (the day of tumor resection surgery )
Title
Early postoperative complications rate after resectional surgery
Description
The rate complications after tumor resection surgery
Time Frame
30 days after resectional surgery
Title
Length of hospital stay after resectional surgery
Description
Number of days spent in hospital after tumor resection surgery
Time Frame
30 days after resectional surgery
Title
Intraoperative complications rate during resectional surgery
Description
The rate of complications during tumor resection surgery
Time Frame
1 day (the day of resectional surgery)
Title
Late complications rate during resectional surgery
Description
The rate of complications after tumor resection surgery
Time Frame
31-90 days after tumor resection surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients are 18 years old or older Stage I-IV according to TNM classification Patients with malignant colonic obstruction Overall health status according to ASA classification: I-III Overall health status according to Charlson comorbidity index ≤ 8 points Signed informed consent with agreement to attend all study visits The patient is not pregnant Exclusion Criteria: Inflammatory bowel disease Acute purulent process in the abdominal cavity The patient wants to withdraw from the clinical trial Loss to follow-up
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Irina Gorovaia, MD
Phone
+79175998459
Email
rudenko@kkmx.com
First Name & Middle Initial & Last Name or Official Title & Degree
Inna Tulina, MD
Phone
+79264086672
Email
tulina@kkmx.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Petr Tsarkov, Prof
Organizational Affiliation
Russian Society of Colorectal Surgeons
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinic of colorectal and minimally invasive surgery University Hospital n2, Clinical Center Sechenov First Moscow State Medical University
City
Moscow
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gorovaia Irina
Phone
007-917-599-84-59
Email
rudenko@kkmx.ru
First Name & Middle Initial & Last Name & Degree
Tsarkov Petr, professor
Phone
007-499-110-32-22
Email
tsarkov@kkmx.ru

12. IPD Sharing Statement

Plan to Share IPD
No
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Self-expandable Metal Stent (SEMS) Endoscopic Placement for Malignant Colonic Obstruction Therapy

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