Application of Somatostatin for Advanced Gastric Cancer After D2 Lymph Node Dissection

NCT ID: NCT01914692

Last Updated: 2013-08-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-31

Study Completion Date

2013-07-31

Brief Summary

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Gastric cancer radical surgery related complications are common.Somatostatin is a conventional medical therapy for bleeding.This study explore the effect of Somatostatin for Advanced Gastric Cancer After D2 Lymph Node dissection.

Detailed Description

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Conditions

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Gastric Cancer After D2 Lymph Node Dissection

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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Somatostatin group

Patients with Advanced Gastric Cancer After D2 Lymph Node Dissection accept the Somatostatin medical therapy.

Group Type EXPERIMENTAL

Somatostatin

Intervention Type DRUG

Somatostatin is a kind of traditional medicines ,which is for the treatment of intestinal fistula,upper gastrointestinal hemorrhage.

Blank group

Use the normal saline instead of somatostatin.

Group Type PLACEBO_COMPARATOR

No interventions assigned to this group

Interventions

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Somatostatin

Somatostatin is a kind of traditional medicines ,which is for the treatment of intestinal fistula,upper gastrointestinal hemorrhage.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. More than eighteen years old
2. Gastric cancer diagnosed by pathological examination
3. Be given informed consent
4. Without diabetes/hyperthyroidism/Damages of functions of heart, liver and kidney/Systemic Infection/immunodeficiency

Exclusion Criteria

1. Contraindication of vascular puncture operation
2. Patients who refused to take part in the programe
3. Poor compliance of treatment
4. Malnutrition,BMI\<18
5. with pancreatectomy
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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First Affiliated Hospital, Sun Yat-Sen University

OTHER

Sponsor Role lead

Responsible Party

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Wang Shaochuan

Postgraduate

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Song Wu, Doctor

Role: STUDY_CHAIR

First Affiliated Hospital of Sun Yat-sen University

Other Identifiers

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nova-0426

Identifier Type: -

Identifier Source: org_study_id