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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00749905
Other study ID # SHEBA-08-5217-SBH-CTIL
Secondary ID
Status Terminated
Phase Phase 2
First received
Last updated
Start date January 2009
Est. completion date December 2009

Study information

Verified date June 2018
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A prospective randomized controlled investigator-blinded study to compare efficacy of low fiber diet for 5 days versus regular diet, both as adjunct to one day clear liquid diet and standard bowel preparation for colon capsule examination


Recruitment information / eligibility

Status Terminated
Enrollment 75
Est. completion date December 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- Age >18 and <75

- Colon study indicated for colo-rectal carcinoma screening

- After colonoscopy for any indication failed due to technical causes

- Patients who decline an indicated colonoscopy

Exclusion Criteria:

- Significant heart failure (NYHA grade III-IV)

- Renal failure (Creatinine > 1.2 mg/dl)

- Known or suspected intestinal strictures

- Known or suspected mesenteric adhesions

- History suggestive of bowel obstruction

- Vomiting and/or aspirations

- Symptoms of dysphagia

- Pace-maker or AICD implanted

- Known allergy or intolerance to any of the study drugs

- Pregnancy

- Illicit drug abuse or alcoholism

- Inability to provide an informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
low fiber diet
Low fiber diet for 5 days prior to colon capsule
regular diet
Regular diet until 1 day before colon capsule

Locations

Country Name City State
Israel Sheba Medical Center Tel-Hashomer

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Colon cleanliness one week from capsule examination
Secondary Tolerability of preparations within 1 day of completing preparation
See also
  Status Clinical Trial Phase
Completed NCT03146052 - Comparison Between Asymmetric And Standard Split-Dose Regimen For Bowel Preparation N/A