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Trial Title:
Reconstruction of the Pelvic Floor and Perineal Wound After Rectal ELAPE
NCT ID:
NCT06066931
Condition:
Rectum Cancer
Conditions: Official terms:
Rectal Neoplasms
Conditions: Keywords:
Cancer of the lower ampullary rectum
Extralevatory abdominal-perineal extirpation
Plastic surgery of the pelvic floor and perineal wound
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Intervention model description:
It is planned to recruit patients over the age of 18, suffering from cancer of the lower
ampullary rectum with T1-T4N0-2M0 (according to the classification of malignant tumors
TNM in the 8th edition) who meet the inclusion criteria taking into account the exclusion
criteria in the number of 150 people. Group 1 is a simple method (Plastic surgery with
local tissues) n=50; Group 2 is plastic surgery with a mesh endoprosthesis n=50; group 3
is a new method of plastic surgery n=50.
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Procedure
Intervention name:
Plastic surgery of the pelvic floor and perineal wound with counter-displaced skin-subcutaneous fascial flaps after extralevatory abdominal-perineal extirpation of the rectum
Description:
Skin-subcutaneous fascial flap on the leg is cut out from one side of the perineal wound,
and deepithelized, forming a diamond-shaped perineal wound. The cut flap is immersed in
the aperture of the pelvis and fixed with single sutures to the remains of levators of
the opposite side. The flap width should be 3-4 cm, sufficient to fill the pelvic
aperture. On the opposite side of the wound, a skin-subcutaneous fascial flap is cut out
on a triangular leg equal to the width of the previously formed diamond-shaped wound. The
flap is moved to the center of the wound, additionally filling wound cavity with it,
combining the vertex of the triangle with the vertex of the rhombus. The perineal wound
is drained through the contraperture. The flap is fixed with separate nodal seams.
Arm group label:
Group 3 is a new method of plastic surgery n=50
Intervention type:
Procedure
Intervention name:
Plastic surgery of the pelvic floor and perineal wound with local tissues
Description:
Simple layer-by-layer suturing of the sciatic-anal and subcutaneous adipose tissue is
performed using nodular sutures. The skin was sewn up with nodular sutures at the
discretion of surgeons. The installation of abdominal drainage and/or perineal drainage
was left to the discretion of the surgeon.
Arm group label:
Group 1 of a simple method (Plastic surgery with local tissues) n=50
Intervention type:
Procedure
Intervention name:
Plastic surgery of the pelvic floor and perineal wound with mesh endoprosthesis
Description:
A mesh allograft with an adhesive coating is inserted into the bottom of the wound,
positioned horizontally between the inner surfaces of the ischial bones and vertically
between the sacrum and the vagina in women or between the sacrum and the prostate gland
in men. The mesh was sewn from behind on both sides of the coccyx or sacrum. From the
side, the mesh was attached to the remainder of the levator muscle and from the front to
the transverse muscles of the perineum. The installation of abdominal drainage and/or
perineal drainage was left to the discretion of the surgeon. The sciatic-anal and
subcutaneous fat are sutured using nodular sutures.
Arm group label:
Group 2 is plastic surgery with a mesh endoprosthesis n=50
Summary:
A multicenter, cohort, randomized, controlled study is being conducted since the 1of
September, 2023 whereby the immediate and long-term results of pelvic floor and perineal
wound plastic surgery after extralevatory abdominal-perineal extirpation of the rectum
will be compared. The study is conducted on the basis of the Federal State Budgetary
Educational Institution of the Ministry of Health Care of the Russian Federation, the
Department of General Surgery at the clinical base of the State Budgetary Healthcare
Institution " Krasnodar Regional Hospital No. 1 named after Professor S.V. Ochapovsky" of
the Ministry of Health Care of the Krasnodar Territory, State Budgetary Healthcare
Institution " Krasnodar Oncological Dispensary No. 1" of the Ministry of Health Care of
the Krasnodar Territory The study included patients over 18 years old suffering from
cancer of the lower ampullary rectum with T1-T4N0-2M0 (according to the classification of
malignant tumors TNM in the 8th edition), who are scheduled for extralevatory
abdominal-perineal extirpation of the rectum. Patients are randomized into 3 groups: the
first group includes patients with plastic surgery in a simple way (Plastic surgery with
local tissues), the second group includes patients with plastic surgery with a mesh
endoprosthesis and the third one includes patients with plastic surgery in a new way.
The purpose of the study is to evaluate the effectiveness of the developed method of
pelvic floor and perineal wound plastic surgery after extralevatory abdominal-perineal
extirpation of the rectum. It is easily reproducible and provides high-quality closure of
the deep and skin defect of the perineal wound. In addition, the new method will reduce
the frequency of postoperative complications when compared with the use of conventional
methods of closing the defect of the perineum, the method improves the quality of life
and provides early rehabilitation of patients.
Study status- patients are being recruited. Number of patients selected is 150 patients.
The primary endpoint of the study is the assessment of the early postoperative period and
the frequency of postoperative complications (Flap necrosis; Suppuration; Hematoma;
Bleeding; Seroma) within 30 days from the date of surgery. The study was approved by the
Independent Ethics Committee Protocol No. 112 of 12th November, 2022.
It is planned to recruit patients within 2 years and monitor each of them for 30 days
after surgery to assess the primary endpoint and to monitor patients within 1 year to
assess the secondary endpoint. The secondary endpoint means an assessment of the
frequency of late postoperative complications (perineal fistula, abscess, hernia) and an
assessment of the quality of life within 1 year after surgery. It is planned to complete
the study in 2025.
Eventually it is planned to publish the protocol of the study, the results obtained after
the recruitment of the required number of patients as well as the results of evaluation
of the primary endpoint.
Detailed description:
The aim of the study is to improve the results of pelvic floor and perineal wound plastic
surgery after extralevatory abdominal-perineal extirpation (EAPE) of the rectum for
cancer of the lower ampullary rectum by applying a new method of plastic surgery.
Being examined according to the standards of cancer treatment of the lower ampullary part
of rectum, patients are hospitalized in the oncological surgery department. In the
preoperative period, they are randomized by the Randomizer program into 3 groups by the
head of the study on the day of surgery: the 1st Group includes patients to be made
plastic surgery in a simple way (Plastic surgery with local tissues), the 2nd Group
includes patients to be made plastic surgery with a mesh endoprosthesis and the 3rd Group
includes patients to be made plastic surgery in a new way.
Patient data, clinical trial results, and randomization results are introduced into the
Microsoft Access database.
The operation is carried out as follows: under combined endotracheal anesthesia after the
completion of the abdominal and pelvic stage of the operation ending with the
mobilization of the rectum which is carried out along the posterior wall to the level of
V sacral vertebra corresponding to the bend of the sacrum; along the anterior wall that
is the level of seminal vesicles, the upper pole of the prostate gland in men, the middle
third of the vagina in women; along the lateral walls reaching the level of the pelvic
nerve plexus and finally a single-stem colostomy is formed.
Suturing of the wound of the anterior abdominal wall with drainage of the pelvic cavity
is performed. The patient is placed on his abdomen with his legs apart - "the position of
a penknife". The operating surgeon is positioned between the patient's legs. Suturing of
the skin of the perianal area with a pouch suture is performed after surgical treatment
and limitation of the surgical area. Re-processing of the operating area is performed. It
is made a fringing incision in the perianal region from the level of the sacrococcygeal
joint, along the perianal-skin folds to the middle of the perineal seam. 2-4 sutures of
wound fiber fixing to the skin of the external gluteal region may be applied for the
purpose of additional traction in patients with severe obesity.
Cylindrical mobilization of the rectum is performed with the capture of sciatic-rectal
fiber and the external sphincter along the posterior and lateral walls. If necessary, to
improve visualization or in case of tumor invasion, the coccyx is amputated. After
crossing the sacro-rectal and anococcygeal ligaments, they are connected to the abdominal
cavity. The pelvic tendon arch is sequentially crossed along the posterolateral walls,
with a transition to the side walls and a wide cut-off of the muscle that raises the anus
from the fixation site to the sciatic bone. After mobilization of the posterior and
lateral semicircles, the drug is turned into the perineal wound and mobilization is
continued along the anterior semicircle. After removal of the rectum with a neoplasm, the
part of it is sent for histological examination. The cavity of the perineal wound is
sanitized with an antiseptic solution. The plastic stage of the operation is performed: -
In group 1 patients (plastic surgery with local tissues), a simple layer-by-layer
suturing of the sciatic-anal and subcutaneous adipose tissue is performed using nodular
sutures. The skin was sewn up with nodular sutures at the discretion of surgeons. The
installation of abdominal drainage and/or perineal drainage was left to the discretion of
the surgeon.
- In group 2 patients, a mesh allograft with an adhesive coating is inserted into the
bottom of the wound, positioned horizontally between the inner surfaces of the
ischial bones and vertically between the sacrum and the vagina in women or between
the sacrum and the prostate gland in men. The mesh was sewn from behind on both
sides of the coccyx or sacrum. From the side, the mesh was attached to the remainder
of the levator muscle and from the front to the transverse muscles of the perineum.
The installation of abdominal drainage and/or perineal drainage was left to the
discretion of the surgeon. The sciatic-anal and subcutaneous fat are sutured using
nodular sutures.
In group 3 patients, the plastic stage is performed as follows: on one side of the
perineal wound, a cutaneous-subcutaneous-fascial flap on the leg is cut out and
deepithelized, along the entire length of the wound, thereby forming a diamond-shaped
perineal wound, plunging it into the pelvic aperture, fixing it with single sutures to
the remnants of the muscle lifting the anus of the opposite side, and the flap width is
3-4 cm, sufficient to fill the pelvic aperture. On the opposite side of the wound, a
triangular skin-subcutaneous fascial flap is cut out on a leg equal to the width of the
previously formed diamond-shaped wound at an angle of 60-80 degrees from the middle of
the wound edge, and the sides of the triangular flap should be equal to half the length
of the edge of the diamond-shaped wound, then it is moved and additionally fill the wound
cavity with it, in condition of displacement of the apex of the triangle flap with the
top of the rhombus-wounds. The perineal wound is drained through the contraperture. The
flap and the edges of the wound are separated from the gluteal muscles and the flap is
fixed with separate skin nodular sutures to eliminate tension.
The results of the operation, the postoperative course and the quality of life are
recorded in the Microsoft Access database with subsequent statistical processing. The
postoperative wound photo is made in the day of discharge (up to 30 days after surgery).
Expected results: after completing the recruitment of patients to the comparison groups
and after statistical processing it is planned to obtain an evidence base on reducing the
frequency of early and late postoperative complications in the group with plastic surgery
in a new way.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
1. Patients over 18 years old suffering from cancer of the lower ampullary rectum
cT1-T4N0-2M0 (according to the classification of malignant tumors TNM in the 8th
edition).
2. Patients with planned extralevatory abdominal-perineal extirpation of the rectum.
3. Physical status of patients according to ASA classification I-II.
4. Signed informed consent to participate in the study.
Non-inclusion criteria:
1. Verification of the squamous cell carcinoma diagnosis.
2. The presence of acute purulent processes in the area of surgical intervention.
Exclusion Criteria:
1. Refusal to participate at any stage of the study.
2. Death in the early postoperative period (up to 30 days after surgery) caused by
somatic complications not associated with surgery (PATE, myocardial infarction,
stroke).
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Start date:
October 1, 2023
Completion date:
October 1, 2026
Lead sponsor:
Agency:
Kuban State Medical University
Agency class:
Other
Collaborator:
Agency:
State Budget Public Health Institution Scientific Research Institute - Ochapovsky Regional Clinical Hospital
Agency class:
Other
Collaborator:
Agency:
City Clinical Oncology Hospital No 1
Agency class:
Other
Source:
Kuban State Medical University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06066931