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CLEANComparative Analysis of the Osmotic Laxative Application Efficiency and Safety Eziclen and Moviprep for Colonoscopy Preparation

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Qué se está evaluando

Eziklen®

+ MoviPrep

Medicamento
Quiénes están siendo reclutados

Enfermedades del colon+8

+ Enfermedades del Sistema Digestivo

+ Neoplasias del sistema digestivo

De 18 a 85 años
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Cómo está diseñado el estudio

Estudio Diagnóstico

Intervencional
Inicio del estudio: junio de 2019
Ver detalles del protocolo

Resumen

Patrocinador PrincipalRussian Society of Colorectal Surgeons
Contacto del EstudioTatiana Garmanova, MDMás contactos
Última actualización: 28 de enero de 2026
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Fecha de inicio: 2 de junio de 2019

Fecha en la que se inscribió al primer participante.

The key method of colorectal examination is colonoscopy. The result, diagnostic significance and therapeutic safety depend a lot on the quality of bowel preparation. One of the main purposes of colonoscopy is detecting the earliest forms of colorectal cancer and prognostically meaningful small nonpolyposis neoplasms. The good and perfect bowel preparation is essential in this case. However, the bowel preparation for colonoscopy must fulfill the following criterias: * Be effective, that means to empty colon of faeces, residual liquid and foamy content fully and safely; * Harmless, no side effects on the other organs and systems; * Do not cause discomfort nor change to electrolyte balance, well tolerated; * Do not affect the severity of bowel disease nor cause macro- and microscopic colon mucose changes; * Quick response with short preparation period (no more than 24 hours); * Easy to use, so patient could perform it independently or with the least medical staff participation; * Do not require special conditions, equipment and staff training (possibility to perform at home); * Do not distort the endoscopic image (colour, shape, reflexion); * Do not limit the use of vital dyes or other means of endoscopic diagnosis and treatment; * Do not damage the endoscopic equipment; * be cheap . Bowel preparation schemes usually include diet (low-residue) and oral laxative intake. The low-residue diet should last no more than 24 hours before the colonoscopy according to the European Society of Gastrointestinal Endoscopy clinical recommendations. The time factor is essential for quality of bowel preparation. If the colonoscopy is performed in the first half of day the intake of the part of laxatives (usually a half) on that day (split-mode or separate) provides a better result in comparison to full dose intake on the colonoscopy day or the evening before it. Bowel preparation might be fully undertaken (in full volume) in the morning of examination day for patients undergoing colonoscopy in the afternoon according to some studies. In the case of laxative intake on the morning of examination day, excellent preparation quality and good patient tolerance was demonstrated in the Varughese S et al. research assessing 4 liters bowel preparation scheme efficiency for patients undergoing colonoscopy in the afternoon in comparison to intake in the evening before colonoscopy. The patient's somatic status and the urgency should be considered for choosing the bowel preparation mode. Polyethyleneglycol-based drugs have become more commonly used in clinical practice for colonoscopy bowel preparation since its appearance in 1980. The drug passes through the intestine without being absorbed and metabolized and increases the bowel liquid volume, as do all osmotic laxatives. Thus, electrolyte balance is not disrupted and effective intestinal lavage occurs. But patient compliance might be influenced significantly due to a large volume intake requirement (4 l) and specific organoleptic feature. Over the course of several years, European and Canadian experts have accepted the sodium picosulfate+ magnesium citrate-based low-volume bowel preparation method (2l) as alternative option and the FDA has also approved it in July 2012. This combined intake scheme allows to prepare intestine efficiently for the examination. The sodium picosulfate has a bowel stimulating effect and as osmotic laxative magnesium citrate retains water. But the electrolyte balance changes and dehydration may also influence the patient compliance to laxative. According to the international clinical recommendations for colonoscopy, 4l polyethylenуglycol-based laxative in split-mode preparation with an time interval no more than 4 hours from the end of preparation until colonoscopy is recommended as a standard method. Low-dose polyethylenуglycol-based laxative intake (2l) combined with ascorbate or sodium thiosulfate+ magnesium citrate can serve as alternative examination preparation method (especially for outpatients). Only polyethylenуglycol-based laxative can be recommended for patients with renal failure as bowel preparation method. Eziclen - potassium, magnesium and sodium sulphates-based osmotic laxative for colonoscopy preparation registered in Russia doesn't have a strong evidence base and is not included in national recommendations yet due to its recent market entry (2018) But according to the registered multicenter controlled clinical trials assessing the potassium, magnesium and sodium sulfates vs. 2l polyethyleneglycol with electrolytes efficiency for colonoscopy preparation in split-mode (n=356) and one-day preparation (n=364) (primary endpoint - bowel purity degree as "perfect", "good", "bad") as well as non-conceded Eziclen efficiency was identified in comparing to the control group (97,2% vs 96,1% and 84% vs 82,9% respectively). The side effects frequency was also comparable with control group. There was shown a comparable rate of effective bowel preparation (97,2% vs 97,7%) on a background of higher patient compliance (95,7 % comparing to 82,3 %) in a similar study assessing Eziclen efficiency, safety and patient compliancy in comparison with Macrogol 400 with electrolytes. So the investigators aimed our study to investigate efficiency, safety and compliance of two low-volume laxatives Potassium Sulfate+ Magnesium Sulfate+ Sodium Sulfate-based (Eziclen) vs. relevant volume of Macrogol-3350+ Sodium Sulfate+ Potassium Chloride+ Sodium Chloride+ Ascorbic Acid and Sodium Ascorbate-based (Moviprep) in bowel preparation for colonoscopy.

Título OficialComparative Analysis of the Osmotic Laxative Application Efficiency and Safety Eziclen and Moviprep for Colonoscopy Preparation
Patrocinador PrincipalRussian Society of Colorectal Surgeons
Contacto del EstudioTatiana Garmanova, MDMás contactos
Última actualización: 28 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 98 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio Diagnóstico

Los estudios diagnósticos se centran en mejorar como se detecta o confirma una enfermedad. Prueban nuevas herramientas o técnicas que podrían ofrecer diagnósticos más rápidos o precisos.


Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

De 18 a 85 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos no permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Enfermedades del colonEnfermedades del Sistema DigestivoNeoplasias del sistema digestivoEnfermedades GastrointestinalesNeoplasias GastrointestinalesEnfermedades IntestinalesNeoplasias IntestinalesNeoplasiasNeoplasias por SitioEnfermedades RectalesNeoplasias colorrectales

Criterios

Inclusion Criteria: 1. Signed informed consent forms confirming the understanding of the course of study and agreement to participate in it. 2. A written patient consent to fill the prepared questionnaire and to perform diagnostic colonoscopy in case of following situations: * Routine oncological screening * Polyps or neoplasms in anamnesis * Anemia or latent bleeding diagnostics * Diarrhea or constipation with unknown reason * Inflammatory bowel disease in remission * Pathological formation according to US examination (neoplasm evidence in abdomen) 3. Suspicious colon neoplasms according to CT and/or irrigography 4. ASA scale for physical status assessment ≤ 3 5. Patients with adequate electrolyte balance rate (K, Na, Cl, bicarbonate rate screening). Non-inclusion criteria: 1. The baseline data about comorbidities or laboratory data that can jeopardize the safety of the patient or reduce the likelihood of obtaining satisfactory data necessary to achieve the goal (goals) of the study. 2. The presence of progressive carcinoma or other bowel disease, leading to excessive mucous membrane fragility. 3. The confirmed or suspected gastrointestinal (FA) obstruction, stagnation in the stomach, gastroparesis, or a violation of gastric evacuation. 4. The intestinal perforation. 5. The profuse vomiting. 6. The procedure goal to perform a medical procedure (eg, polypectomy, mucosectomy). 7. The presence of toxic colitis or megacolon. 8. Severe acute phase of inflammatory bowel disease as a contraindication to colonoscopy. 9. The presence of acute GI bleeding. 10. History of gastrointestinal surgery (for example, colostomy, colectomy, gastric bypass surgery, stomach resection). 11. The history of impaired consciousness predisposing to pulmonary aspiration. 12. The colonoscopy aimed remove a foreign body or decompression. 13. History of incomplete colonoscopy 14. The confirmed severe renal failure (glomerular filtration rate (GFR) \<30 ml / min / 1.73 m2). 15. The confirmed severe liver failure (10-15 points on the Child-Pugh scale). 16. Dehydration condition requiring treatment. 17. The ascites. 18. Severe congestive heart failure (class III and IV). 19. The state of hyperuricemia with a clinic of gouty arthritis. 20. Pregnancy or lactation. 21. Patients at risk of pregnancy and not using an acceptable method of contraception during the study. Women of childbearing age must provide a negative pregnancy test at the beginning of the study and must use the oral contraceptive method, double (use a condom with spermicidal gel, birth control suppositories or films; diaphragm with spermicides; or male condom and diaphragm with spermicides), injection contraception or intrauterine devices . Non-fertile women - more than a year after menopause, after surgical sterilization or hysterectomy at least 3 months before the start of the study. 22. The hypersensitivity reaction to active substances or to other auxiliary substances (Eziklen and Moviprep). 23. A patient with a mental state that does not allow him to understand the nature, extent and possible consequences of the study and / or evidence of refusal to cooperate. 24. During the course of the study, the patient is likely to require treatment with drugs that are not permitted by the study protocol. Exclusion Criteria: 1. The pregnancy 2. The inability to follow the protocol 3. Refuse of study participation.

Plan de Estudio

Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.
Grupos de Tratamiento
Objetivos del Estudio

2 grupos de intervención están designados en este estudio

0% de probabilidad de ser asignado al grupo placebo

Grupos de Tratamiento

Grupo I

Comparador Activo
potassium, magnesium and sodium sulphates-based laxative

Grupo II

Comparador Activo
Macrogol-3350 + Sodium Sulfate + Potassium Chloride+ Sodium Chloride + Ascorbic Acid-based and Sodium Ascorbate-based Moviprep

Objetivos del Estudio

Objetivos Primarios

Objetivos Secundarios

Centros del Estudio

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Este estudio tiene una ubicación

Reclutando

Clinic of Colorectal and Minimally invasive surgery

Moscow, RussiaAbrir Clinic of Colorectal and Minimally invasive surgery en Google Maps
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