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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01603654
Other study ID # Low volume preparations
Secondary ID
Status Completed
Phase Phase 4
First received May 17, 2012
Last updated May 21, 2012
Start date January 2011
Est. completion date September 2011

Study information

Verified date May 2012
Source Ospedale L. Sacco – Polo Universitario
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

Adequate bowel cleansing is essential for effective colonoscopy. Acceptance of colon preparation affects the quality of colon cleansing. The study is aimed at comparing the efficacy, safety and acceptability of sodium picosulphate/magnesium citrate (PMC) and low-volume PEG -ascorbic acid (PEG+ASC)in colon cleansing, and to identify predictors of poor bowel preparation.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date September 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- adult outpatients

- aged 18-85 years

- undergoing elective colonoscopy

Exclusion Criteria:

- previous colon resection

- ileus

- intestinal obstruction

- toxic megacolon

- severe heart failure (New York Heart Association [NYHA] Class III or IV)

- acute cardiovascular disease

- uncontrolled arterial hypertension (systolic pressure > 170 mmHg, diastolic pressure > 100 mmHg)

- severe liver failure or ascites

- end-stage renal failure

- phenylketonuria

- glucose-6-phosphate dehydrogenase deficiency. Women were excluded from the study if they were pregnant, breastfeeding

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
sodium picosulphate magnesium citrate
Use of the product in colon cleansing before colonoscopy. Two sachets each containing 10 mg of sodium picosulfate, 3.5 g magnesium oxide and 12.0 g citric acid. The 2 doses are taken diluted in a glass water.
low-volume PEG -ascorbic acid
THe product is used as colon cleanser before colonoscopy. It is supplied as a powder for oral use, to be reconstituted with 2 L of water and drunk as a solution. It consists of 100.0 g macrogol 3350 plus electrolytes (7.5 g sodium sulphate, 2.7 g sodium chloride, 1.0 g potassium chloride) and 4.7 g ascorbic acid.

Locations

Country Name City State
Italy Ospedale Valduce, Gastroenterologia Como
Italy Ospedale L. Sacco, Endoscopic Unit Milano
Italy Ospedale S. Paolo Milano

Sponsors (1)

Lead Sponsor Collaborator
Ospedale L. Sacco – Polo Universitario

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy of bowel cleansing Assessment of quality of colon cleansing at colonoscopy as achieved by the two study products Within 24 hrs No
Secondary Safety Occurrence of complications related to the intake or the two study products In the 24 hours within assumption of study products Yes
Secondary Tolerability Acceptability of the two study products in term of palatability and ease to take the products Within 12 hrs Yes