Skip to content

Risk Stratified Multidisciplinary Ambulatory Management of Malignant Bowel Obstruction in Gynecological Cancers

Risk Stratified Multidisciplinary Ambulatory Management of Malignant Bowel Obstruction (MAMBO) Program for Women With Advanced Gynecological Cancers

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03260647
Acronym
MAMBO
Enrollment
96
Registered
2017-08-24
Start date
2017-08-04
Completion date
2024-12-31
Last updated
2025-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynecologic Cancer

Brief summary

Management of Malignant Bowel Obstruction (MBO) in Patients with Advanced Gynecological Cancers

Detailed description

Guidelines for the management of patients with Malignant Bowel Obstruction(MBO) are not available and as such, there remains an urgent need for a collaborative approach to streamline patient care and optimize use of hospital resources. This study will focus on management of MBO in advanced gynecological cancers.If patients with MBO can be effectively managed in an ambulatory setting, this may improve quality and consistency of patient care, and help reduce volume and duration of bed occupancy.

Interventions

OTHERManagement algorithm for Malignant Bowel Obstruction

a proposed management algorithm for MBO has been developed to provide a pathway that safeguards quality and continuity of care for patients under a multidisciplinary team. It will engage key-stakeholders and foster an inter-professional approach. It incorporates an in-patient management algorithm and a novel nursing-led ambulatory management algorithm to supplement patient's medical management

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Histologically and /or cytologically confirmed gynecological cancer, including ovarian, fallopian tube, endometrial, cervical or primary peritoneal cancer Deemed to be at risk of developing or have a clinical diagnosis of MBO as defined using the following criteria: clinical evidence of bowel obstruction (history/physical/radiological examination; and bowel obstruction beyond the ligament of Treitz.

Exclusion criteria

There are no specified

Design outcomes

Primary

MeasureTime frameDescription
Optimization of multidisciplinary care2 yearsTo optimize the multidisciplinary care management of MBO in patients with advanced gynecological cancer treated at University Health Network (UHN) which include in-patient and ambulatory management algorithm for MBO • Measured by a ratio of days alive and out of hospital compare to days in hospital within the first 60 days after diagnosis of MBO

Secondary

MeasureTime frameDescription
Evaluation of impact of MBO management on hospital visits2 yearsTo evaluate the impact of MBO management on number of emergency room visits, hospital admission and number of days alive and outside of hospital within the first 168 days (6 months) after the diagnosis of MBO
Evaluation of impact of MBO management on patient reported outcomes2 yearsTo evaluate the impact of ambulatory MBO management on patient reported outcomes using the Distress Assessment & Response Tool (DART)
To evaluate nutritional status of patients with MBO2 yearsTo evaluate the nutritional status of patients with MBO • Measured by monthly albumin and weight
Evaluation of clinico-pathological factors2 yearsTo evaluate the clinico-pathological factors that may predict benefit from palliative surgery, chemotherapy and total parenteral nutrition (TPN)
Evaluation of treatment outcomes2 yearsTo evaluate the treatment outcomes of patients with MBO * Measured by resolution of MBO and overall survival * Measured by transition through specific bowel management colour code system
Determine percentage number of patient microbiome sample analyses completed1.5 yearsTo record the percentage of patients who agree to, and for whom sample collection and analysis is completed
Record changes in the sum and types of gut microbiome from baseline to study end1.5 yearsChanges in the sum as well as types of microbiomes as recorded at baseline, initiation of total parenteral nutrition, incidence of an MBO and end of study are to be recorded
Evaluate cannabis use in patient population1.5 yearsAssess for any relationship between cannabis use and MBO
Improve patient understanding and awareness of MBO2 yearsTo improve patients' understanding and awareness of MBO with patient education material.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026