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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01284764
Other study ID # HGI-2011-01
Secondary ID
Status Completed
Phase Phase 3
First received January 26, 2011
Last updated October 4, 2011
Start date January 2011
Est. completion date September 2011

Study information

Verified date October 2011
Source Inje University
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

A low volume of water intake and mosapride will effectively reduce food residue in remnant stomach for patients who had undergone subtotal gastrectomy due to gastric cancer.


Description:

We evaluate that a 500mL of water intake and mosapride will effectively reduce food residue in remnant stomach for patients who had undergone subtotal gastrectomy due to gastric cancer. We plan to compare this method with routine midnight fasting method for endoscopy in patients with subtotal gastrectomy.


Recruitment information / eligibility

Status Completed
Enrollment 144
Est. completion date September 2011
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Outpatients who had subtotal gastrectomy for gastric cancer

Exclusion Criteria:

- Pregnancy

- Lactation

- History of anastomotic stricture

- Recurrent advanced gastric cancer

- Poor general condition( > 2 ECOG)

- Other disseminated malignancy

- Significant renal failure or congestive heart failure (CHF)

- Liver failure

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Drug:
Mosapride
Mosapride 10mg, one dosage, once evening of the day before the endoscopy

Locations

Country Name City State
Korea, Republic of Haeundae Paik Hospital, Inje University School of Medicine Busan

Sponsors (1)

Lead Sponsor Collaborator
Inje University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Degrees of food residue using endoscopic scoring system We plan to evaluate how much a low volume of water and mosapride, compared with routine fasting, reduse food residue in gastric remnant for endoscopy. six months Yes
Secondary Tolerability of a low volume of water and mosapride We plan to evaluate tolerability of a low volume of water and mosapride compared with routine fasting for endoscopy preparation in patients with subtotal gastrectomy six months Yes