MedPath

Investigation of the Effect of Senagraph on colon preparatio

Phase 3
Recruiting
Conditions
Chronic Kidney Disease.
Chronic kidney disease (CKD)
Registration Number
IRCT20180412039283N2
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
122
Inclusion Criteria

Patients with Chronic Kidney Disease (GFR<60) who are candidates for colonoscopy

Exclusion Criteria

Patients needing dialysis or Patients with a GFR of less than 15 (Base on MDRD)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bowel preparation quality base on Ottawa score. Timepoint: 24 hours after receiving the solution. Method of measurement: perform colonoscopy and determine the Ottawa score.
Secondary Outcome Measures
NameTimeMethod
Blood Urea Nitrogen(BUN). Timepoint: Before the intervention, 24 hours and 48 hours after the intervention. Method of measurement: Blood biochemistry test.;Ceratinin(Cr). Timepoint: Before the intervention, 24 hours and 48 hours after the intervention. Method of measurement: Blood biochemistry test.;Sodium(Na). Timepoint: Before the intervention, 24 hours and 48 hours after the intervention. Method of measurement: Blood biochemistry test.;Potasium(K). Timepoint: Before the intervention, 24 hours and 48 hours after the intervention. Method of measurement: Blood biochemistry test.
© Copyright 2025. All Rights Reserved by MedPath