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Early Surgery Versus 3 Days Non-surgical Management in Acute Small Bowel Obstruction (SURGI-BOW) (SURGI-BOW)

Primary Purpose

Small Bowel Obstruction

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Standard support
Early surgery proposed according to the radiological score
Sponsored by
University Hospital, Angers
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Small Bowel Obstruction

Eligibility Criteria

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

Inclusion Criteria: Admission for acute intestinal obstruction of the small intestine on adhesion or bridle Confirmation of the aSBO by a scanner Adult patient Beneficiary of a social security scheme Having signed an informed consent Exclusion Criteria: Indication for urgent surgery (small intestine ischemia, intestinal pain, defence, hemodynamic shock, etc.) Pregnancy or breastfeeding Poor understanding of the French language Person deprived of liberty by judicial or administrative decision Person undergoing psychiatric treatment under duress Person subject to a legal protection measure Person unable to express consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Standard support

    Early surgery proposed according to the radiological score

    Arm Description

    Initial medical treatment: placement of a nasogastric tube associated with hydration and vascular filling for hypovolaemic patients. Other medical treatments for occlusive small bowel syndrome on adhesion or flange can be performed but are not systematically recommended. Their use is left to the discretion of the surgeon. Medical treatment is carried out over 72 hours from admission. In case of resumption of a transit by gas and/or stools associated with a tolerance to the food, the exit is authorized without resorting to surgery. In the absence of a resumption of transit by gas and/or stools associated with tolerance to food, semi-urgent surgical management is proposed 72 hours from the start of management. In the event of deterioration of the clinical condition during hospitalization, urgent surgery will be proposed, according to the recommendations for use.

    Patients included in the experimental arm have treatment adapted to the radiological score. The radiological score described by Berge et al. (Berge et al. Eur J Trauma Emerg Surg 2021) is calculated after patient inclusion.

    Outcomes

    Primary Outcome Measures

    90-day morbidity and mortality of aSBO management using the radiological score
    The main objective is to evaluate the effectiveness, in terms of 90-day morbidity and mortality, of management of uncomplicated aSBO based on the use of the radiological score as a tool to select patients eligible for early surgery. compared to standard care (medical treatment for 72 hours).

    Secondary Outcome Measures

    Morbidity and mortality at 30 days
    Morbidity and mortality at 30 days of aSBO management
    Length of patient hospitalization
    Time between admission and discharge from hospitalization
    Recurrence rate of aSBO
    Recurrence rate of aSBO after the episode. Recurrence is defined by any admission of the patient for nausea/vomiting and absence of flatulence and stools with a CT scan showing distension of the small intestine within one year of admission.
    Rate of recourse to surgery for patients not operated on straight away
    Recourse to surgery is defined by a surgical intervention carried out for the treatment of aSBO
    Surgical morbidity and mortality at 30 days of patients operated on during the first hospitalization
    Surgical morbidity and mortality at 30 days of aSBO management defined as the appearance of a deviation from the normal course of expected surgical outcomes between the day of hospitalization and the 30th day. Morbi-mortality is classified according to the Dindo-Clavien scale. Morbi-mortality is collected only for surgical patients, and if the episode is secondary to surgical treatment.
    Laparoscopic surgery rate
    Laparoscopic surgery rate is defined as the number of surgeries performed from incision to closure by laparoscopic approach out of the total number of surgeries. The need for conversion by laparotomy will also be collected and compared between the 2 groups

    Full Information

    First Posted
    September 13, 2023
    Last Updated
    September 26, 2023
    Sponsor
    University Hospital, Angers
    Collaborators
    Direction Générale de l'Offre de Soins
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06065150
    Brief Title
    Early Surgery Versus 3 Days Non-surgical Management in Acute Small Bowel Obstruction (SURGI-BOW)
    Acronym
    SURGI-BOW
    Official Title
    SURGI-BOW - Early Surgery Versus 3 Days Non-surgical Management in Acute Small Bowel Obstruction: a Randomized Open-label Controlled Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 2, 2024 (Anticipated)
    Primary Completion Date
    January 1, 2027 (Anticipated)
    Study Completion Date
    January 1, 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Hospital, Angers
    Collaborators
    Direction Générale de l'Offre de Soins

    4. Oversight

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

    5. Study Description

    Brief Summary
    For uncomplicated acute small bowel obstruction (aSBO), the "Bologna guidelines" recommend non-surgical management of 72 hours before considering surgery. This treatment is based on the placement of a nasogastric tube and the correction of hydro-electrolyte disorders. Non-surgical management is only effective in 60 to 70% and surgery is therefore necessary in 30 to 40% of cases after medical treatment for at least 3 days. This therefore leads to an increase in the length of hospital stay. Some authors also point out that postponing surgery for 3 days would aggravate the morbidity and mortality of surgery. Indeed, aSBO surgery has a complication rate of 10-40% and a mortality of up to 4%. There is a lack of studies evaluating what is the best management strategy for aSBO, especially with regard to the duration of medical treatment. Many recent studies plead in favor of early surgical treatment (<24 hours) which would reduce the morbidity and mortality rate of surgery but also the overall cost of treatment by reducing the length of stay. This paradigm shift is linked to the improvement of anesthetic and intensive care management over the last few years, but also to the advent of laparoscopy in emergency surgery. Indeed, laparoscopy could reduce the duration of hospitalization but also the operative morbidity and mortality. However, this surgical approach is not feasible in all situations and the conversion rate is reported in 30 to 76% of cases. One of the factors favoring the feasibility of the laparoscopic approach is the performance of early surgery. Another parameter favoring the feasibility of the laparoscopic approach is the aSBO mechanism: an aSBO on flange (SBA) is more likely to be treated effectively by laparoscopic than an aSBO on multiple adhesions (MA). In the literature, there is little to differentiate SBAs from MAs. Advances in CT scans have made it possible to describe the signs associated with the SBA mechanism and then to propose a score making it possible to predict the SBA mechanism with good performance (sensitivity 67.6%, specificity 84.6%). This score not only has the advantage of predicting the mechanism of the occlusion but it also makes it possible to predict the failure of non-surgical treatment if the score is ≥5.
    Detailed Description
    Multicentre randomized open-label controlled trial. Patients admitted to visceral surgery for aSBO are screened and the study is offered for patients who do not meet the criteria for emergency surgery. If they accept the study, a randomization is carried out by stratification according to (i) the sex, (ii) the center (University hospital/ Peripheral center), (iii) the number of previous episodes of aSBO (0 or ≥1 ) and the value of the radiological score (< or ≥5). Patients are cared for according to the strategy defined by randomisation (standard procedure vs early surgery proposed according to the radiological score). Demographic information, medical and surgical history, and treatments are collected on the day of admission. A visit is made each day (from admission to discharge) to collect information on the surgery (if performed), on the medical management and its success or failure (if applicable), on the recovery of functions gastrointestinal, on perioperative management, on morbidity and mortality. Patients have a follow-up consultation on D30 and D90 postoperative. Any morbidity, mortality or recurrence that occurred during this period is collected. Patients are contacted by telephone after 12 months to ensure that no recurrence of aSBO has occurred.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Small Bowel Obstruction

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Multicentre randomized open-label controlled trial
    Masking
    None (Open Label)
    Masking Description
    non applicable
    Allocation
    Randomized
    Enrollment
    630 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Standard support
    Arm Type
    Active Comparator
    Arm Description
    Initial medical treatment: placement of a nasogastric tube associated with hydration and vascular filling for hypovolaemic patients. Other medical treatments for occlusive small bowel syndrome on adhesion or flange can be performed but are not systematically recommended. Their use is left to the discretion of the surgeon. Medical treatment is carried out over 72 hours from admission. In case of resumption of a transit by gas and/or stools associated with a tolerance to the food, the exit is authorized without resorting to surgery. In the absence of a resumption of transit by gas and/or stools associated with tolerance to food, semi-urgent surgical management is proposed 72 hours from the start of management. In the event of deterioration of the clinical condition during hospitalization, urgent surgery will be proposed, according to the recommendations for use.
    Arm Title
    Early surgery proposed according to the radiological score
    Arm Type
    Experimental
    Arm Description
    Patients included in the experimental arm have treatment adapted to the radiological score. The radiological score described by Berge et al. (Berge et al. Eur J Trauma Emerg Surg 2021) is calculated after patient inclusion.
    Intervention Type
    Procedure
    Intervention Name(s)
    Standard support
    Intervention Description
    See arm/group descriptions
    Intervention Type
    Procedure
    Intervention Name(s)
    Early surgery proposed according to the radiological score
    Intervention Description
    If score ≥ 5: the risk of medical treatment failure is multiplied by 2.9 (Feuerstoss F et al, J Gastrointest Surg 2021). Early surgical treatment is proposed; that is, the procedure is performed within 24 hours of admission. The surgery is initiated by laparoscopy and converted to open surgery if necessary. If score < 5: the risk of medical treatment failure is reduced. Initial medical treatment is therefore offered in accordance with standard management.
    Primary Outcome Measure Information:
    Title
    90-day morbidity and mortality of aSBO management using the radiological score
    Description
    The main objective is to evaluate the effectiveness, in terms of 90-day morbidity and mortality, of management of uncomplicated aSBO based on the use of the radiological score as a tool to select patients eligible for early surgery. compared to standard care (medical treatment for 72 hours).
    Time Frame
    90 days
    Secondary Outcome Measure Information:
    Title
    Morbidity and mortality at 30 days
    Description
    Morbidity and mortality at 30 days of aSBO management
    Time Frame
    30 days
    Title
    Length of patient hospitalization
    Description
    Time between admission and discharge from hospitalization
    Time Frame
    assessed to 2 days
    Title
    Recurrence rate of aSBO
    Description
    Recurrence rate of aSBO after the episode. Recurrence is defined by any admission of the patient for nausea/vomiting and absence of flatulence and stools with a CT scan showing distension of the small intestine within one year of admission.
    Time Frame
    one year
    Title
    Rate of recourse to surgery for patients not operated on straight away
    Description
    Recourse to surgery is defined by a surgical intervention carried out for the treatment of aSBO
    Time Frame
    One year
    Title
    Surgical morbidity and mortality at 30 days of patients operated on during the first hospitalization
    Description
    Surgical morbidity and mortality at 30 days of aSBO management defined as the appearance of a deviation from the normal course of expected surgical outcomes between the day of hospitalization and the 30th day. Morbi-mortality is classified according to the Dindo-Clavien scale. Morbi-mortality is collected only for surgical patients, and if the episode is secondary to surgical treatment.
    Time Frame
    30 days
    Title
    Laparoscopic surgery rate
    Description
    Laparoscopic surgery rate is defined as the number of surgeries performed from incision to closure by laparoscopic approach out of the total number of surgeries. The need for conversion by laparotomy will also be collected and compared between the 2 groups
    Time Frame
    Surgery time assessed to 1 hour

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Admission for acute intestinal obstruction of the small intestine on adhesion or bridle Confirmation of the aSBO by a scanner Adult patient Beneficiary of a social security scheme Having signed an informed consent Exclusion Criteria: Indication for urgent surgery (small intestine ischemia, intestinal pain, defence, hemodynamic shock, etc.) Pregnancy or breastfeeding Poor understanding of the French language Person deprived of liberty by judicial or administrative decision Person undergoing psychiatric treatment under duress Person subject to a legal protection measure Person unable to express consent
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Paul Le Naoures, Dr
    Phone
    (0)2 41 35 49 16
    Ext
    33
    Email
    Paul.LeNaoures@chu-angers.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Aurélien Vénara, Pr
    Phone
    (0)2 41 35 36 18
    Ext
    33
    Email
    AuVenara@chu-angers.fr
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Cécile Jaglin-Grimonprez
    Organizational Affiliation
    University hospital of Angers
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    Early Surgery Versus 3 Days Non-surgical Management in Acute Small Bowel Obstruction (SURGI-BOW)

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