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PEG Versus PEG+Bisacodyl Versus Sennosides for Colon Cleansing Before Colonoscopy

Phase 4
Completed
Conditions
Colonoscopy Preparation
Interventions
Drug: polyethylene glycol +Bisacodyl
Registration Number
NCT01531140
Lead Sponsor
Medical University of Warsaw
Brief Summary

Background:

Polyethylene glycol (PEG) solution has been proven to be effective for large bowel cleansing prior to colonoscopy in children. However, the high volume of fluid and its taste sometimes lead to inappropriate cleansing of the bowel, thus search for other bowel preparation is needed.

Aim:

The efficacy and tolerability of three different bowel cleansing protocols used in children for colonoscopy: high-volume PEG compared with low-volume PEG with stimulant laxative (bisacodyl) compared with sennosides.

Methods:

Participants aged 10-18 years will be randomly assigned to receive either PEG 60 ml/kg/day or PEG 30 ml/kg/day plus oral bisacodyl 10-15 mg/day or sennosides 2mg/kg/day for 2 days prior to the colonoscopy. The outcome measures will be:bowel cleansing efficacy, scored by a blinded endoscopist using the Ottawa scale and Aronchick Scale (the mean total score, proportions of participants with excellent/good and with poor/inadequate bowel preparation), and the patient satisfaction score(0-10)with the method of preparation for the colonoscopy evaluated with the visual analog scale. Analysis will be done on an intention to treat basis.

Detailed Description

Patients are excluded if they had known allergy to one of the tested preparations such as bisacodyl (Bisacodyl VP, ICN Polfa, Rzeszow, Poland), polyethylene glycol (Fortrans, Beaufour Ipsen Industry, Dreux, France) and/or sennoside (Xenna Extra, US Pharmacia, Wroclaw, Poland) and had disorders that make oral intake of the preparation impossible (neurological disorders, intestinal obstruction, mental retardation etc.).

Study design:

On admission day patients are allocated to one of the groups by study investigators, according to the randomization list created by an independent person using block randomization by a standard statistical program StatsDirect \[version 2,3,8 (2005)\] (6 patients were included in each block).

During the preparation for colonoscopy each patient are observed for procedure tolerance. On the day of endoscopy, each patient evaluated the degree of the acceptance of the method of bowel cleaning (according to visual analog scale (VAS) and the occurrence of side effects (diary). The endoscopist performing colonoscopy, blinded for the bowel preparation regimen evaluate bowel cleansing and score it, according to the Aronchick and Ottawa scale. The rate of cecum intubation, and the colonoscopy complications (defined as bowel perforation and/or significant bleeding) are analyzed in each bowel preparation group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
240
Inclusion Criteria
  • children 10 - 18 years of age referred for colonoscopy
  • informed consent signed
Exclusion Criteria
  • allergy to PEG, sennosides or bisacodyl
  • disorders that make oral intake of the preparation impossible (neurological disorders, intestinal obstruction, mental retardation etc.)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Polyethylene glycolPolyethylene glycolPolyethylene glycol p.o.(Fortrans):60 ml/kg for 2 days
PEG + Bisacodylpolyethylene glycol +BisacodylPolyethylene glycol p.o.(Fortrans): 30 ml/kg for 2 days + Bisacodyl p.o.: 10-15 mg/day
SennosidesSennosidesSennosides: 1tbl/8kg/day for 2 days (1 tbl=8,6 mg sennosides B)
Primary Outcome Measures
NameTimeMethod
proportions of participants with good or excellent bowel preparation assessed with Ottawa Scalebowel preparation quality with Ottawa scale is assesed during colonoscopy (3rd day of the study) by endoscopist blinded for the method of preparation

According to the Ottawa scale the quality of bowel preparation is estimated by adding points for the cleansing of three parts of colon (descending, transversal and ascending) and points for amount of fluid in the bowel. Score: 0-1 - excellent cleansing, 2-4 - good, 5-7 - sufficient, 8-10 - poor, 11-14 - not appropriate.

proportions of participants with poor/inadequate bowel preparation assessed with Ottawa Scalebowel preparation quality with Ottawa scale is assesed during colonoscopy (3rd day of the study) by endoscopist blinded for the method of preparation

According to the Ottawa scale the quality of bowel preparation is estimated by adding points for the cleansing of three parts of colon (descending, transversal and ascending) and points for amount of fluid in the bowel. Score: 0-1 - excellent cleansing, 2-4 - good, 5-7 - sufficient, 8-10 - poor, 11-14 - not appropriate.

Secondary Outcome Measures
NameTimeMethod
proportions of participants with very good/good bowel preparation assessed with Aronchick Scalebowel preparation quality with Aronchick scale is assesed during colonoscopy (3rd day of the study) by endoscopist blinded for the method of preparation

According to Aronchick scale preparation is estimated as:

* very good: small amount of clear fluid is present, more than 95% mucosa is visible

* good: small amount of clear fluid easy to suction away or flush is present, more than 90% of mucosa is visible

* sufficient: big amount of clear fluid covering 5-25% of mucosa, more than 90% of mucosa visible

* poor: semi-liquid stool that cannot be flushed, less than 90% of mucosa visible

* inadequate: colonoscopy must be repeated

proportions of participants with poor/inadequate bowel preparation assessed with Aronchick Scalebowel preparation quality with Aronchick scale is assesed during colonoscopy (3rd day of the study) by endoscopist blinded for the method of preparation

According to Aronchick scale preparation is estimated as:

* very good: small amount of clear fluid is present, more than 95% mucosa is visible

* good: small amount of clear fluid easy to suction away or flush is present, more than 90% of mucosa is visible

* sufficient: big amount of clear fluid covering 5-25% of mucosa, more than 90% of mucosa visible

* poor: semi-liquid stool that cannot be flushed, less than 90% of mucosa visible

* inadequate: colonoscopy must be repeated

mean bowel preparation score assessed with Ottawa Scalebowel preparation quality with Ottawa scale is assesed during colonoscopy (3rd day of the study) by endoscopist blinded for the method of preparation

According to the Ottawa scale the quality of bowel preparation is estimated by adding points for the cleansing of three parts of colon (descending, transversal and ascending) and points for amount of fluid in the bowel. Score: 0-1 - excellent cleansing, 2-4 - good, 5-7 - sufficient, 8-10 - poor, 11-14 - not appropriate.

mean bowel preparation score assessed with Aronchick scalebowel preparation quality with Aronchick scale is assesed during colonoscopy (3rd day of the study) by endoscopist blinded for the method of preparation

According to Aronchick scale preparation is estimated as:

* very good: small amount of clear fluid is present, more than 95% mucosa is visible

* good: small amount of clear fluid easy to suction away or flush is present, more than 90% of mucosa is visible

* sufficient: big amount of clear fluid covering 5-25% of mucosa, more than 90% of mucosa visible

* poor: semi-liquid stool that cannot be flushed, less than 90% of mucosa visible

* inadequate: colonoscopy must be repeated

patient satisfaction with the method of preparation assessed with Visual analogue scale (VAS)assessed by patient after completion of bowel preparation regimen before colonoscopy (3rd day of the study)

VAS scale is horizontal line 100 mm lenght anchored by word description at each end (very good, very bad).The patient mark on the line the point that feel represent the perception of bowel preparation regimen.

Trial Locations

Locations (2)

Warsaw Medical University

🇵🇱

Warsaw, Poland

Child Health Center

🇵🇱

Warsaw, Poland

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