Surgery for Obstructed Gastric Carcinoma
Palliative Resection Versus Palliative Bypass in Obstructed Locally Advanced Gastric Carcinoma
1 other identifier
interventional
63
1 country
1
Brief Summary
The goal of this clinical trial is to find the best treatment for obstructed gastric carcinoma in gastric cancer patients. It will include all patients with obstructed gastric cancer with different ages and sex who consented to share in the trial. The main question is what is the better for management for obstructed gastric cancer; palliative resection or palliative bypass? We hypothesized that resection is better. patients will be divided into two groups. the primary outcome measure will be the relief of obstruction
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable gastric-cancer
Started Feb 2026
Shorter than P25 for not_applicable gastric-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
February 19, 2026
CompletedFirst Posted
Study publicly available on registry
February 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
February 27, 2026
February 1, 2026
1 year
February 19, 2026
February 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
upper gastrointestinal symptoms
upper gastrointestinal symptoms will be evaluated after surgery by Rhodes Index questionnaire. It is a validated, self-report instrument used to measure the intensity, frequency, and distress of upper gastrointestinal symptoms. The scale measures three main areas: nausea (frequency, duration, distress), vomiting (amount, frequency, distress), and retching (frequency, distress). It utilizes a 5-point Likert scale (0-4) to quantify the severity of these symptoms. 0 is the least amount of distress and 4 is the most distress.
from one day to two weeks after surgery
Secondary Outcomes (4)
anastmotic leak
from day one to two weeks after surgery.
ICU admission
from day one to two weeks after surgery
wound infection
from day one to one month after surgery
mortality
from one day to one month after surgery
Study Arms (2)
Group I: obstructed gastric cancer patients
ACTIVE COMPARATORpatients presented with emergency gastric obstruction
Group II: obstructed gastric cancer patients
ACTIVE COMPARATORpatients presented with emergency gastric obstruction
Interventions
distal, subtotal or total gastrectomy with gastro-jejunostomy or eosphago-jejunostomy will be done
palliative gastro-jejunostomy or eosphago-jejunostomy will be done
Eligibility Criteria
You may qualify if:
- emergency obstructed gastric cancer patients
You may not qualify if:
- non obstructed gastric cancer patients
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
faculty of medicine, Zagazig University
Zagazig, Sharqia Province, 44519, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Reham Zakaria, M.D
Zagazig University, Egypt
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- lecturer of general surgery
Study Record Dates
First Submitted
February 19, 2026
First Posted
February 27, 2026
Study Start
February 1, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
February 1, 2027
Last Updated
February 27, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
data will be available on demand by contacting the principle investigator