- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07238166
Benign Versus Malignant Causes of Intussuception in Adults
Benign Versus Malignant Causes of Intussuception in Adults : A Prospective Study in Assiut University Hospital
The aim of this study is to evaluate adult intussecption :
- Prevalence of benign vs malignant causes.
- Distribution by anatomical type.
- Clinical presentation patterns.
- Diagnostic accuracy of imaging.
- Surgical approach and outcomes.
- Length of hospital stay, complications, recurrence
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Intussusception is a condition characterized by the invagination of one segment of the intestine into another, leading to obstruction and potentially ischemia (1). While intussusception is relatively common in the pediatric population, it is considered a rare clinical entity in adults, accounting for only 1-5% of all cases and approximately 1% of intestinal obstructions in the adult population. The etiology, clinical presentation, and management of adult intussusception differ significantly from pediatric cases, necessitating a distinct clinical approach (2).
In contrast to children, where most cases are idiopathic, adult intussusception is commonly associated with an underlying pathological lead point. In approximately 70-90% of adult cases, a structural lesion can be identified as the cause of the intussusception (3). These lesions may be benign or malignant in nature and understanding the incidence of each is important for appropriate diagnosis and treatment planning (4).
In general, intussusceptions involving the small intestine are more likely to be caused by benign lesions such as lipomas, polyps, or Meckel's diverticulum, whereas those involving the colon have a higher likelihood of being associated with malignancy, especially primary adenocarcinoma (5).
Adult intussusception poses a diagnostic challenge due to its nonspecific and often chronic symptoms, which may include intermittent abdominal pain, nausea, vomiting, gastrointestinal bleeding, or signs of partial bowel obstruction (6).
The advent of advanced imaging techniques, particularly abdominal computed tomography (CT), has improved the preoperative diagnosis of this condition (7). However, surgical exploration remains the definitive diagnostic and therapeutic modality, especially given the high probability of underlying malignancy (8).
Despite advancements in diagnostic imaging and surgical techniques, there remains a lack of general agreement regarding the optimal management of adult intussusception, particularly concerning the necessity and extent of bowel resection when a benign cause is suspected (9). Moreover, data on the relative incidence of benign versus malignant causes vary widely across regions, institutions, and populations.
This study aims to evaluate adult intussecption, prevalence of benign versus malignant causes in AUH.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Andrew gamal fikry, MBBCH, MSc ( general surgury )
- Phone Number: +201224173419
- Email: gamalandrew751@gmail.com
Study Locations
-
-
-
Asyut, Egypt
- Department of general surgury Assiut uneversity hospital
-
Contact:
- Andrew gamal fikry, MBBCh, MSc (general surgury)
- Phone Number: +201224173419
- Email: gamalandrew751@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
a. Inclusion criteria:
Age ≥ 19 years.
• Confirmed diagnosis of intussusception by: Imaging (CT , ultrasound , or barium studies) Intraoperative findings,
- Patients managed surgically with documented follow-up and final diagnosis. b. Exclusion criteria:
- Patients with incomplete records or lost to follow-up
- Intussusception diagnosed radiologically but resolved spontaneously without confirmatory intervention or follow-up
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Adult patient with intussusception
Adult patient with intussusception will undergo surgical resection followed byhistopathological evaluation to determine the underlying causes ( benign or malignant )
|
Adult patient diagnosed with intussusception will undergo surgical resection of affected bowel segment under general anathesia .
the resected specimens will be sent for histopathological evalution to determine the underlying cause , whether benign (e.g lipoma , polyp )or malignant (e.g adenocarcinama , lymphoma ).
operative finding , postoperative outcome , and pathology results will be recorded and analyzed
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
prevalence of benign versus malignant causes
Time Frame: 2 weeks after surgical resection
|
Histopathological examination of resected bowel specimens will determine whether the cause of intussusception is benign (e.g., lipoma, polyp) or malignant (e.g., adenocarcinoma, lymphoma).
The frequency and percentage of each category will be calculated
|
2 weeks after surgical resection
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation between preoperative imaging findings and histopathological results Description
Time Frame: At the time of diagnosis (preoperative period )
|
Evaluate the diagnostic accuracy of preoperative imaging (CT scan findings such as target sign, mass lesion) in predicting benign or malignant pathology
|
At the time of diagnosis (preoperative period )
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Operative findings
Time Frame: During intraoperative period
|
To record intraoperative findings including location of intussusception (small bowel, ileocecal, colocolic), presence of lead point, bowel viability, and type of surgical procedure
|
During intraoperative period
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Intussusception in adult
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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