The aim of this study is to evaluate the quality, acceptance, tolerability and adverse effects of colonoscopy preparations with the different available preparation guidelines.
Study Type
OBSERVATIONAL
Enrollment
126
The high volume electrolytes PEG will be administered at a 4 mg/kg dose the day before the procedure in 4-8 hours.
The low volume electrolytes PEG will be administered at a 4 mg/kg dose the day before the procedure in 4-8 hours.
The Sodium picosulfate will be administered the day before the procedure at different doses depending on the patient´s age: * From 1 to 2 years old: ¼ sachet reconstituted in ¼ glass of water/juice in the afternoon (15:00 h) and ¼ sachet reconstituted in ¼ glass of water/juice 6 hours later (21:00 h) * From 2 to 4 years old: ½ sachet in ½ glass of water/juice in the afternoon and ½ sachet in ½ glass of water/juice at night. * From 4 to 9 years old: 1 sachet in 1 glass of water/juice in the afternoon and ½ sachet in ½ glass of water/juice at night. * Of 9 years old and older: 1 sachet in the afternoon and 1 sachet at night.
Hospital Universitario Puerta del Mar
Cadiz, Cádiz, Spain
NOT_YET_RECRUITINGComplejo Hospitalario Torrecárdenas
Almería, Spain
NOT_YET_RECRUITINGHospital Materno-Infantil de Badajoz
Badajoz, Spain
Evaluate the quality of the colonoscopy preparations in our autonomic community comparing different preparation guidelines : Boston Scale
The quality of the preparations will be measured using the Boston Bowel Preparation Scale (BBPS), semiquantitative evaluation of the cleanliness of the three colon sections (left, transverse, right) using a score from 0 to 3, giving a total score of 0 (without preparation) to 9 (optimal) and it´s done by two independent observers.
Time frame: From November 2018 to December 2019
Evaluate the acceptance of the different preparations.
The acceptance will be measured using a questionnaire and a quantity record, the questonnaire is made by three items: flavour, odour and volume while the quantity record measures the quantity of preparation ingested by the participant.
Time frame: From November 2018 to December 2019
Evaluate the tolerance of the different preparations.
The tolerance will be measured using a questionnaire and a symptoms record, with a score from 0 (terrible tolerance) to 3 (good tolerance) for each of its items, that are the following: abdominal pain, nausea and vomit, intestinal noises, abdominal distension, burps, flatulences, urgent bowel movements and tenesmus.
Time frame: From November 2018 to December 2019
Evaluate the security of the different preparations.
The security will be measured analysing the existence of adverse effects due to the different preparations.
Time frame: From November 2018 to December 2019
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Hospital Universitario Reina Sofía
Córdoba, Spain
NOT_YET_RECRUITINGHospital Universitario Virgen de las Nieves
Granada, Spain
NOT_YET_RECRUITINGHospital Universitario Virgen Macarena
Seville, Spain
RECRUITINGHospital Universitario Virgen del Rocío
Seville, Spain
RECRUITINGInstituto Hispalense de Pediatría
Seville, Spain
NOT_YET_RECRUITING