RecruitingPhase 3NCT07465705

Clinical Trial on Bowel Preparation Comparing Mannitol 100g to Plenvu Both in a Same Day Regimen (CLEARWAY)

A Phase III, International, Multicenter, Randomized, Parallel-group, Endoscopist-blinded Non-inferiority Study of the Efficacy, Safety and Patient Acceptance of Mannitol Versus Plenvu® in Bowel Preparation for Elective Colonoscopy. CLEARWAY


Sponsor

NTC srl

Enrollment

412 participants

Start Date

Sep 2, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a study to test the non-inferiority of bowel cleansing with 100 g Mannitol against standard Plenvu® same-day dosing regimen. The 50% of the subjects will receive Mannitol, while the remaining part will receive Plenvu®.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Ability of subject to consent and provide signed written informed consent.
  • Age ≥ 18 years.
  • Males and females scheduled for elective colonoscopy performed according to ESGE guidelines.
  • Subjects willing and able to complete the entire study and to comply with instructions.

Exclusion Criteria21

  • Pregnancy or breast feeding. Females of childbearing potential must have a negative pregnancy test at Visit 2 and practice highly effective methods of birth control throughout the study period, according to the CTCG "Recommendations related to contraception and pregnancy testing in clinical trials" v 1.2* (unless postmenopausal or surgically sterile, or whose sole sexual partner had a successful vasectomy).
  • Severe acute and chronically active inflammatory bowel disease; subjects in clinical remission (Crohn's Disease Activity Index - CDAI < 150 for Crohn Disease (Best et al. 1976) and Partial Mayo Score ≤ 2 for Ulcerative Colitis (Schroeder et al. 1987)) are allowed.
  • Severe renal failure: eGFR < 30 ml/min/1.73 m2 estimated by simplified MDRD equation.
  • Severe heart failure: New York Heart Association (NYHA) Class III-IV.
  • Severe anaemia (Hb ≤ 8 g/dl).
  • Chronic liver disease Child-Pugh class B or C.
  • Electrolyte disturbances (baseline values of Na2+, Cl-, K+ out of normal ranges).
  • Clinically significant alterations of baseline haemato-chemical parameters.
  • Recent (< 6 months) symptomatic acute ischemic heart disease.
  • History of significant gastrointestinal surgeries, including colon resection, sub-total colectomy, abdominoperineal resection, de-functioning colostomy or ileostomy, Hartmann's procedure and other surgeries involving the structure and function of the colon.
  • History of paralysis of the gut (ileus).
  • History of disorders of gastric emptying (e.g. gastroparesis, gastric retention, etc.).
  • History of phenylketonuria (due to presence of aspartame).
  • History of glucose-6-phosphate dehydrogenase deficiency (due to presence of ascorbate).
  • History of toxic megacolon.
  • Use within 24 hours prior to colonoscopy of laxatives, colon motility altering drugs and/or other substances (e.g., simethicone) that could affect bowel cleansing or visibility during colonoscopy.
  • Suspected bowel obstruction or perforation.
  • Indication for partial colonoscopy.
  • Subjects who received an investigational drug or therapy within 5 half-lives of the first visit.
  • Hypersensitivity to the active ingredients or to any of the excipients of the study drugs.
  • Underwater colonoscopy instead of standard gas insufflation.

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Interventions

DRUG100g of Mannitol

Participants should self administer the preparation within 45 minutes, dissolving 100g of powder in 1L of water

DRUG1L PEG-Asc

Self administration of the same day preparation according to the on lable instruction for use. The first dose consists in dissolving Dose 1 in 500ml of water, followed by another 500ml of water, all within 1 hour. After a 1 hour wait from the end of the first dose, the participant should self administer the Dose 2 consisting in dissolving one sachetA and one sachetB in 500ml of water, followed by another 500ml of water; all within 1 hour.


Locations(18)

Hopital Erasme

Anderlecht, Belgium

Katholieke Universiteit te Leuven

Leuven, Belgium

Algemeen Ziekenhuis Damiaan Oostende

Ostend, Belgium

Azienda Unita Sanitaria Locale Di Modena - Ospedale Ramazzini di Carpi

Carpi, Modena, Italy

Centro Di Riferimento Oncologico Di Aviano

Aviano, Pordenone, Italy

IRCCS Ospedale Sacro Cuore Don Calabria

Negrar, Verona, Italy

Azienda Ospedaliero-Universitaria Di Bologna IRCCS Istituto Di Ricerca E Di Cura A Carattere Scientifico

Bologna, Italy

Fondazione Poliambulanza

Brescia, Italy

Congregazione Delle Suore Infermiere Dell'Addolorata - Ospedale Valduce

Como, Italy

Fondazione IRCCS Cà Granda Ospedale Policlinico

Milan, Italy

Istituto Europeo di Oncologia

Milan, Italy

Policlinico Universitario A. Gemelli

Roma, Italy

Azienda Provinciale Per I Servizi Sanitari

Trento, Italy

H-T.Centrum Medyczne Sp. z o.o. sp.k.

Tychy, Poland

Klinika Reuma Park Sp. z o.o. S.K.

Warsaw, Poland

Narodowy Instytut Onkologii Im. Marii Sklodowskiej-Curie Panstwowy Instytut Badawczy

Warsaw, Poland

Hospital Clinic De Barcelona

Barcelona, Spain

Region Oerebro Laen

Örebro, Sweden

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NCT07465705