Ulcer Peptic Clinical Trial
— ULTRAOfficial title:
The Incidence of Gastrojejunostomy Ulceration After MGB-OAGB: Comparison of Hand-Sewn and Stapled Techniques of Anastomosis Formation. Multicenter Prospective Randomized Clinical Trial Study
We assume that the frequency of gastrojejunostomy ulcers after MGB-OAGB is associated with the peculiarities of the side-to-side gastrojejunostomy (GJS) formation, which is currently the "gold standard" for this procedure. The geometry of such anastomosis leads to the formation of a narrow strip of the gastric wall between two stapler lines (between the suture from the 2nd cassette during the formation of the "small ventricle" and directly from the suture from the cassette during the GJS formation). Perhaps this section of the stomach wall is prone to ischemia, which can certainly increase the risk of ulcer formation. It is also possible that a zone with impaired blood supply may also form in the "blind pocket" above the anastomosis. When forming a Hand-Sewn GJS of the end-to-side type, ischemia zones do not occur. The anastomosis has a more physiological geometry, there is no conflict between the lines of stapled sutures. Thus, we put forward the assumption that a serious risk factor for the development of a GJS ulcer was eliminated when switching to a completely manual technique for the GJS formation when performing MGB-OAGB. The study is aimed at the compare the incidence of GJS ulcers during MGB-OAGB, depending on the techniques of anastomosis formation.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | April 2025 |
Est. primary completion date | April 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Men and women aged 18 to 65; - Body mass index over 40 kg/m2 or 35 kg/m2 in the presence of concomitant metabolic disorders (type 2 diabetes mellitus, hypertension, coronary artery disease, atherosclerosis and dyslipidemia); - Preliminary consultation with an endocrinologist; - Voluntary informed consent for surgical treatment; - Voluntary informed consent to participate in a clinical trial; - A negative test for Helicobacter pylori or a full course of eradication therapy. Non-Inclusion Criteria: - smoking; - gastric ulcer disease in history; - earlier abdominal surgery by laparotomy - abdominal wall hernias; - contraindications to planned operative treatment of bariatric profile based on the results of the pre-surgery evaluation of somatic status (see section "Patient's Treatment Protocol"); - for women - pregnancy planning in the next 12 months; - mental health record; - patients with oncological diseases; Exclusion Criteria: - surgical complications in the early post-surgery period related to the disruption of vital functions of organs and systems (respiratory, neurological and cardiological disorders requiring a stay in then the intensive-care unit, long-term position compression syndrome with renal impairment, venous thromboembolism); - surgical complications in the early post-surgery period requiring repeated surgery or minimally invasive surgery (intraabdominal / intraluminal hemorrhage, failure of manual/ hardware suture on gastrointestinal organs etc.); - positive intraoperative test for leak-proof anastomosis (injection of methylene blue solution or "bubble-test"), requiring surgical procedures for color leakage zone removal (see section "Patient's Treatment Protocol"); - poor adherence to the recommendations for gastroprotective therapy and recommendations on diet after surgery by the patient (see section "Interim control"); - patient's refusal to participate in the clinical study at any stage. |
Country | Name | City | State |
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Russian Federation | Almazov National Medical Research Centre | Saint Petersburg |
Lead Sponsor | Collaborator |
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Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health |
Russian Federation,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The presence of a gastrojejunostomy ulcer | Video endoscopy of the upper gastrointestinal tract | 6 months | |
Secondary | Erosive anastomositis | Video endoscopy of the upper gastrointestinal tract | 6 months | |
Secondary | Time of surgery | Operation time from skin incision to completion of skin suturing | Intraoperative indicator | |
Secondary | The amount of foreign non-absorbable material remaining in the body | The number of cartridges from staplers used during the operation is counted | Intraoperative indicator |
Status | Clinical Trial | Phase | |
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Recruiting |
NCT03736824 -
Correlation of Endoscopic Findings and Symptoms in Patients Undergoing the First Upper Gastrointestinal Endoscopy
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