Performance of NER1008 Enema Compared With Fleet® Enema in Bowel Cleansing

Colorectal Cancer Clinical Trial

Official title:

A Clinical Investigation to Demonstrate the Performance of NER1008 Enema in Bowel Cleansing Compared to Fleet® Enema

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02468726
• Other study ID #: NER1008-01/2011 (ENE)
• Status: Completed
• Phase: N/A
• First received: June 9, 2015
• Last updated: June 10, 2015
• Start date: November 2011
• Est. completion date: December 2012

Study information

• Verified date: November 2011
• Source: Norgine
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

In order for flexible sigmoidoscopy to be a successful screening procedure, the bowel must be free of solid matter so the endoscopist has a clear view, increasing the chance of detection of abnormalities. This is achieved through the use of bowel cleansing preparations, which are administered prior to the procedure. Enemas are the preferred method as they clear the lower bowel more quickly than oral formulations and do not require dietary restrictions.

The medical device being tested in this clinical investigation is NER1008, an enema which contains PEG3350 (polyethylene glycol 3350). PEG3350 is an osmotic agent, which holds the water content in the rectum and sigmoid colon, consequently increasing stool volume, resulting in rectal distension and subsequent distal colon emptying. The increased colonic luminal content stimulates the motility, propulsive transportation and rectal evacuation of the distal colon content.

This study is designed to assess the performance of NER1008 in bowel cleansing and compare this with the performance of Fleet® enema, which is widely used for this purpose.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: December 2012
• Est. primary completion date: March 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Healthy male or female subjects [as determined by medical history, physical examination, laboratory test values, vital signs and 12-lead electrocardiograms (ECG's) at screening] aged 18 to 45 years.

2. Non-smokers from 3 months before enema administration and for the duration of the clinical investigation.

3. Body mass index (BMI) = 18 and = 35 kg/m2.

4. Must voluntarily provide written informed consent to participate in the clinical investigation.

5. Must understand the purposes and risks of the clinical investigation and agree to follow the restrictions and schedule of procedures as defined in the clinical investigation plan, and as confirmed during the informed consent process.

6. Female subjects must be postmenopausal (for at least one year and confirmed by a serum follicle stimulating hormone (FSH) test at screening), surgically sterile, practising true sexual abstinence or must use an effective method of contraception.

7. Female subjects of child-bearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test at check-in of each period.

8. The subject's primary care physician must confirm that there is nothing in their medical history that would preclude their enrolment into this clinical investigation.

9. Must be willing to consent to have data entered into The Over Volunteering Prevention System (TOPS).

Exclusion Criteria:

1. Subjects with a history or presence of significant cardiovascular disease, pulmonary, hepatic, gallbladder or biliary tract, renal, haematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic or psychiatric disease.

2. Subjects with a history or presence of organic or functional gastrointestinal conditions (e.g. chronic constipation, irritable bowel syndrome, inflammatory bowel disease).

3. Subjects with a clinically relevant history or presence of abnormal gastrointestinal motility.

4. Subjects with a significant history of hereditary bowel disorders.

5. Subjects with abnormal findings on the digital rectal examination performed at screening.

6. Use of laxatives or motility altering drugs in the 3 months preceding enema administration.

7. Use of any prescription or over-the-counter medication (including vitamins, herbal and mineral supplements) within 14 days prior to enema administration (or within 5 half lives if longer), with the exception of Investigator-approved hormonal contraceptives, hormone replacement therapy (HRT) and occasional paracetamol.

8. Participation in a clinical drug study during the 30 days preceding enema administration in this clinical investigation.

9. Donation of blood or blood products within 30 days prior to enema administration or during the clinical investigation, except as required for this clinical investigation

10. Pregnant or lactating females.

11. Any clinically significant illness within 28 days prior to enema administration.

12. History or presence of any significant drug allergy, or a known allergy or contraindication to polyethylene glycols, Fleet® enema or midazolam.

13. Laboratory values at screening which are deemed to be clinically significant, unless agreed in advance by the Sponsor's Medical Representative and Principal Investigator.

14. Positive for human immunodeficiency virus (HIV), hepatitis B or hepatitis C.

15. Current or history of drug or alcohol abuse within the 12 months prior to enema administration, or a positive drugs of abuse test at screening or check-in.

16. Consumption of alcoholic beverages within 24 hours of confinement or during confinement.

17. Subjects who, in the opinion of the Investigator, are unsuitable for participation in the clinical investigation.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Screening

Related Conditions & MeSH terms

• Colorectal Cancer

Intervention

Device:
• NER1008 enema
NER1008 enema administered to cleanse the bowel bewteen 1 and 3 hours prior to flexible sigmoidoscopy

Drug:
• Fleet
Fleet enema administered to cleanse the bowel bewteen 1 and 3 hours prior to flexible sigmoidoscopy

Locations

Country	Name	City	State
United Kingdom	BioKinetic Europe Ltd	Belfast

Sponsors (1)

Lead Sponsor	Collaborator
Norgine

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Success of bowel cleansing	Whether recto-sigmoid bowel cleansing has been successful, based on an endoscopist's assessment of the quality of cleansing in the rectum and colon, according to the modified Harefield cleansing scale.	Up to 3 hours	No
Secondary	Grade of bowel cleansing	Grade of bowel cleansing (A, B, C or D), based on an endoscopist's assessment.	Up to 3 hours	No
Secondary	Quality of cleansing in rectum	Quality of cleansing in the rectum based on the modified Harefield cleansing scale (0-4).	Up to 3 hours	No
Secondary	Quality of cleansing in sigmoid colon	Quality of cleansing in the sigmoid colon based on the modified Harefield cleansing scale (0-4)	Up to 3 hours	No
Secondary	Quality of cleansing in the descending colon	Quality of cleansing in the descending colon to the splenic flexure based on the modified Harefield cleansing scale (0-4)	Up to 3 hours	No
Secondary	Depth of scope progression	Prior to removing the endoscope, the depth of progression it has made, in cms	Up to 3 hours	No
Secondary	Stool weight	Weight of stool during the one hour period after the administration of the enema	Up to 3 hours	No