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OpenTrials
Enrolling by Invitation

NCT Number: NCT06817551

Comparison of Outcomes of Management of Bowel Obstruction Pilot Study

The Comparison of Outcomes of Management of Bowel Obstruction (COMBO Pilot) Pilot trial is a patient-level randomized trial of a short course of dexamethasone + supportive care vs supportive care alone for patients with adhesion-related small bowel obstruction (aSBO). The goal of the COMBO trial is to answer the question: Can Dexamethasone increases the proportion of patients with resolution of aSBO with non-operative management (without complication) based on an established minimal important clinical difference.

Enrolling by Invitation

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Washington Medical Center

Seattle, Washington, 98195, United States

About this study

Millions of Americans each year experience adhesion-related small bowel obstruction (aSBO), a condition associated with significant morbidity and prolonged hospitalization. Adhesions formed after previous abdominopelvic surgery can cause twisting of the bowel resulting in injury and a cascade of inflammation that results in progressive bowel wall edema with narrowing of the bowel lumen. This leads to or worsens the bowel obstruction. Reversing this inflammation has the potential to reduce the severity and impact of aSBO, hasten the return of bowel function and avoid an emergency operation to treat the obstruction. Dexamethasone, administered intravenously 2-3 times/day for 5-7 days, has been found effective in patients with a form of SBO related to malignancy (malignant ascites or metastatic disease). A Cochrane review evaluated three RCTs of dexamethasone in patients with malignant SBO and found "evidence that dexamethasone…may bring about the resolution of bowel obstruction" and avoid the need for surgical interventionxx . An underappreciated aspect of these RCTs is that almost all patients had a history of abdominopelvic surgery. Since it is difficult to distinguish the extent to which an SBO is caused by adhesions from prior surgery or mass effect related to malignant ascites or metastases, we hypothesize that dexamethasone may be efficacious in resolving aSBO as well.

The Comparison of Outcomes of Management of Bowel Obstruction (COMBO) study is a double-blinded randomized study of a short course of dexamethasone and supportive care vs. supportive care alone for patients with aSBO. The primary outcome is resolution of SBO without operative management and/or major complications as defined using modified National Surgical Quality Improvement Program (NSQIP) criteria. Differences in secondary outcomes-clinical, healthcare utilization and patient-reported outcomes will be explored overall and across subgroups (e.g., based on severity of aSBO, history of aSBO, sex). Reducing inflammation with dexamethasone- a readily available and safe intervention - may improve the likelihood of non-operative management of aSBO and could change the management of millions of patients with this condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults ≥18 years of age recruited from UWMC
  • Patients presenting to surgical services through the Emergency Department, diagnosis of SBO, consulted by surgeon, and an urgent or emergency operation is deemed not necessary by surgeon.
  • Diagnosis of aSBO is established by;
  • CT findings consistent with diagnosis of SBO; and
  • signs and symptoms consistent with SBO; and
  • Adhesions are the likely cause of SBO (absence of incarcerated hernia, internal hernia, masses, fistula, stricture, volvulus, acute episode of inflammatory bowel disease (IBD) flare, etc.).
  • Ability to provide written or electronic informed consent in English and answer teach-back questions

Exclusion criteria

  • Signs and symptoms of peritonitis with emergency operation planned
  • Planned urgent operation within the next 12 hours
  • Allergy to dexamethasone
  • Surgery within prior 6 weeks
  • Unable or unwilling to return or be contacted for and/or complete research surveys
  • Currently incarcerated in a detention facility or in police custody (patients wearing a monitoring device can be enrolled) at baseline/screening
  • Individuals with latent infections who have an increased risk of infection.

Treatment and study plan

Dexamethasone

Drug

*Please see description for dexamethasone + supportive care arm.

Supportive Care

Other

*Please see description for supportive care arm.

Primary outcomes

  1. Resolution of aSBO

    Time frame: 30 days

    The primary outcome is the resolution of aSBO, defined as the absence of obstruction symptoms, in patients receiving dexamethasone + supportive care compared to those receiving supportive care alone.

Secondary outcomes

  1. Hospital readmissions - 1 Year

    Time frame: 1 Year

    The outcome for this aim is the comparison of healthcare utilization (e.g., readmissions) between the dexamethasone and supportive care groups

  2. Patient-Reported Outcomes (PROs) - GIQLI

    Time frame: 30 days

    The outcome will be the comparison of patient-reported outcomes of gastrointestinal quality of life (GIQLI) between the dexamethasone and supportive care groups.

  3. Hospital readmissions - 30 day

    Time frame: 30 day

    The outcome for this aim is the comparison of healthcare utilization (e.g., readmissions) between the dexamethasone and supportive care groups

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Registry information

Official study title

Comparison of Outcomes of Management of Bowel Obstruction (COMBO) Pilot

Acronym: COMBO Pilot

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Feb 10, 2025
Registry last updated
Mar 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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