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A Phase 3 Clinical Trial to Efficacy and Safety study of KKM-151 for Bowel Cleansing prior to Colonoscopy

Efficacy and Safety study of KKM-151 for Bowel Cleansing prior to Colonoscopy: Randomized, Active-controlled, Single blind(assessor-blinded), Multi-center Phase III Clinical Trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CRIS
Registry ID
KCT0005093
Enrollment
250
Registered
2020-06-05
Start date
2018-03-28
Completion date
Unknown
Last updated
2020-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : 1. Test drug: KKM-151 -How to take and dose: 4 to 5 hours before colonoscopy, take 1 cup (230 ml) of this drug and 460 mL (230 mL * 2 cups) of water during 30 minutes. Repeat this process for a

Sponsors

Yonsei University Health System, Gangnam Severance Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1. Men or women between 19 and 79 years of age. 2. Subject who are scheduled for an elective colonoscopy. 3. Ability to complete the entire procedure and to comply with study instructions. 4. Will provide completed and signed written informed consents

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1. Subjects with hypersensitivity to any ingredients in the study medications. 2. Subjects with known or suspected ileus, gastrointestinal obstruction, gastrointestinal ulcer, intestinal perforation, gastroparesis, gastric outlet obstruction, toxic colitis, mega colon, severe ulcerative colitis and inflammatory bowel disease. 3. Subjects with gastrointestinal surgery such as colectomy or gastrectomy(except simple polyp resection), or with acute surgical abdominal conditions(e.g. acute appendicitis). 4. Subjects with clinically significant abnormal laboratory values of electrolytes at screening, - Na : <130 mmol/L or >150 mmol/L - K: <3.0 mmol/L or >5.5 mmol/L - Corrected serum Ca: <8.0mg/dL(2.0mmol/L) or >11.5mg/dL(2.9mmol/L) 5. Subjects with severe renal disease (serum creatinine > 2.0mg/dL at screening) 6. Subjects having severe congestive heart failure(NYHA III, IV) within previous 3 months at signing consents. 7. Subjects with ascites of any etiology. 8. Subjects with severe abdominal distension or abdominal pain 9. Subjects with history of phenylketonuria, glucose-6-dehydrogenase deficiency 10. Rhabdomyolysis patients 11. Subjects prone to lung aspiration and who fall under one of the following: -Those with conscious disabilities, those with vomiting reflex disorders, those with nasogastric tube feeding, patients with dysphagia 12. Subjects with active malignancy 13. Subjects taking any other investigational medications within 3 months prior to screening. 14. Subjects who should continuously take medications which could derange water or electrolyte balance during interventional period (diuretics, Angiotensin converting enzyme(ACE) inhibitor, Systemic corticosteroids, Digoxin, Lithium) 15. Subjects with childbearing potential without an effective method of birth control (e.g. oral contraceptive, intrauterine device, surgical sterilization, hysterectomy) or pregnant or lactating women. 16. Subjects who is classified not suitable for this study by investigators

Design outcomes

Primary

MeasureTime frame
Success rate of colon cleanliness evaluated by an independent evaluator using the Harefield Cleansing Scale

Secondary

MeasureTime frame
Colon cleansing success rate evaluated by colonoscopists using Harefield Cleansing Scale;Overall satisfaction evaluated by colonoscopist;Subject questionnaire evaluation about the total volume of drugs;Subject questionnaire evaluation about the taste of drugs;Subject questionnaire evaluation about the difficulty of ingestion of drugs;Whether or not to re-use, subject questionnaire evaluation;Evaluate the number of bowel movements during the period of intake using subject’s diary;Overall satisfaction with taking method, subject questionnaire evaluation;Intracolonic flammable gas concentration

Countries

Korea, Republic of

Contacts

Public ContactJaejun Park

Yonsei University Health System, Severance Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026