NCT07435025

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
63

participants targeted

Target at P25-P50 for not_applicable gastric-cancer

Timeline
6mo left

Started Feb 2026

Shorter than P25 for not_applicable gastric-cancer

Geographic Reach
1 country

1 active site

Status
active not recruiting

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 Progress51%
Feb 2026Feb 2027

Study Start

First participant enrolled

February 1, 2026

Completed
18 days until next milestone

First Submitted

Initial submission to the registry

February 19, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 27, 2026

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2027

Last Updated

February 27, 2026

Status Verified

February 1, 2026

Enrollment Period

1 year

First QC Date

February 19, 2026

Last Update Submit

February 24, 2026

Conditions

Keywords

gastrectomypalliativebypass

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 COMPARATOR

patients presented with emergency gastric obstruction

Procedure: palliative gastric resection

Group II: obstructed gastric cancer patients

ACTIVE COMPARATOR

patients presented with emergency gastric obstruction

Procedure: palliative bypass

Interventions

distal, subtotal or total gastrectomy with gastro-jejunostomy or eosphago-jejunostomy will be done

Group I: obstructed gastric cancer patients

palliative gastro-jejunostomy or eosphago-jejunostomy will be done

Group II: obstructed gastric cancer patients

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Stomach Neoplasms

Condition Hierarchy (Ancestors)

Gastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesStomach Diseases

Study Officials

  • Reham Zakaria, M.D

    Zagazig University, Egypt

    PRINCIPAL INVESTIGATOR

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

Locations