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Efficacy and Safety of Bowel Preparations for Colonoscopy in Spinal Cord Injury (SCI)

This study is not yet open for participant recruitment.
Verified by Department of Veterans Affairs, September 2008

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00745095
  Purpose

The annual incidence of colorectal cancer in the US during 2005 was approximately 150,000 cases and this neoplasm claimed 56,000 lives (American Cancer Society). Detection (and removal) of colonic polyps is now the central strategy in reducing the risk of colon cancer. Thus, failure to detect and remove small cancers and polyps can have dire consequences. Although it has not been shown that persons with spinal cord injury (SCI) have an increased risk of this disease, there is no reason to assume that the incidence after SCI would be less than that of the general population.

Colonoscopy would appear to be a better approach to colon cancer screening after SCI but may also be unreliable if bowel evacuation is unsatisfactory for complete large bowel visualization. Poor colonoscopic visualization is a major concern in persons with SCI because they have long-standing difficulty with evacuation (DWE) and might not respond in a predictable or satisfactory manner to the conventional bowel preparations used for colonoscopy. Furthermore, to the extent that bowel preparation for colonoscopy is unsatisfactory in persons with SCI, the putative benefits of colonoscopy in reducing colon cancer mortality may not be realized.

In the absence of effective regimens for bowel preparation in persons with SCI, we suspect that the documented benefits of screening colonoscopy in the able-bodied may not generalize to persons with SCI. Regardless, these observations support the need for improved bowel preparation approaches in persons with SCI. One such approach might involve the adjunctive administration of prokinetic drugs to standard practices. A prokinetic agent that might be beneficial in this context is neostigmine, an anticholinesterase inhibitor with prominent parasympathomimetic actions (stimulation of peristalsis) on the colon. We have studied neostigmine extensively in persons with SCI and have shown that, when given in combination with glycopyrrolate, this approach to stimulate bowel evacuation is safe and effective for bowel evacuation.


Condition Intervention Phase
Spinal Cord Injury
Drug: Neostigmine
Phase IV

MedlinePlus related topics:   Cancer    Spinal Cord Injuries   

Drug Information available for:   Neostigmine    Neostigmine bromide    Neostigmine Methylsulfate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Diagnostic, Randomized, Single Blind (Outcomes Assessor), Factorial Assignment, Safety/Efficacy Study
Official Title:   Efficacy and Safety of Bowel Preparations for Colonoscopy in SCI

Further study details as provided by Department of Veterans Affairs:

Primary Outcome Measures:
  • Quality of bowel preparation [ Time Frame: 1-2 days following intervention ] [ Designated as safety issue: No ]

Estimated Enrollment:   480
Study Start Date:   November 2008
Estimated Study Completion Date:   November 2012
Estimated Primary Completion Date:   November 2011 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: No Intervention
(SCI, GFR<=60) Polyethylene glycol prep only
2: Experimental
(SCI, GFR<=60) Polyethylene glycol prep and neostigmine
Drug: Neostigmine
Neostigmine will be administered in 20, 40, and 60mg doses until an individualized dose-response relationship is established
3: No Intervention
(SCI, GFR>=60) OSPS only
4: Experimental
(SCI, GFR>=60) OSPS + NG
Drug: Neostigmine
Neostigmine will be administered in 20, 40, and 60mg doses until an individualized dose-response relationship is established
5: No Intervention
(SCI, GFR>=60) PEG only
6: Experimental
(SCI, GFR>=60) NG + PEG
Drug: Neostigmine
Neostigmine will be administered in 20, 40, and 60mg doses until an individualized dose-response relationship is established
7: No Intervention
(SCI, GFR>=60) OSPS + PEG
8: Experimental
(SCI, GFR>=60) OSPS + PEG + NG
Drug: Neostigmine
Neostigmine will be administered in 20, 40, and 60mg doses until an individualized dose-response relationship is established
9: No Intervention
(Control, GFR>=60) OSPS
10: No Intervention
(Control, GFR>=60) PEG only
11: No Intervention
(Control, GFR>=60) OSPS + PEG

Detailed Description:

The annual incidence of colorectal cancer in the US during 2005 was approximately 150,000 cases and this neoplasm claimed 56,000 lives (American Cancer Society). Detection (and removal) of colonic polyps is now the central strategy in reducing the risk of colon cancer. Thus, failure to detect and remove small cancers and polyps can have dire consequences. Although it has not been shown that persons with spinal cord injury (SCI) have an increased risk of this disease, there is no reason to assume that the incidence after SCI would be less than that of the general population.

Colonoscopy would appear to be a better approach to colon cancer screening after SCI but may also be unreliable if bowel evacuation is unsatisfactory for complete large bowel visualization. Poor colonoscopic visualization is a major concern in persons with SCI because they have long-standing difficulty with evacuation (DWE) and might not respond in a predictable or satisfactory manner to the conventional bowel preparations used for colonoscopy. Furthermore, to the extent that bowel preparation for colonoscopy is unsatisfactory in persons with SCI, the putative benefits of colonoscopy in reducing colon cancer mortality may not be realized.

In the absence of effective regimens for bowel preparation in persons with SCI, we suspect that the documented benefits of screening colonoscopy in the able-bodied may not generalize to persons with SCI. Regardless, these observations support the need for improved bowel preparation approaches in persons with SCI. One such approach might involve the adjunctive administration of prokinetic drugs to standard practices. A prokinetic agent that might be beneficial in this context is neostigmine, an anticholinesterase inhibitor with prominent parasympathomimetic actions (stimulation of peristalsis) on the colon. We have studied neostigmine extensively in persons with SCI and have shown that, when given in combination with glycopyrrolate, this approach to stimulate bowel evacuation is safe and effective for bowel evacuation.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

1. SCI and able-bodied patients with clinical indication for a colonoscopic examination

Exclusion Criteria:

  1. Able-bodied patients with a GFR 60ml/min.
  2. SCI and able-bodied patients who are not candidates for elective colonoscopy (i.e., those with recent myocardial infarction, terminal illness, etc.)
  3. SCI and able-bodied patients who have a contraindication to PEG administration (i.e., those with colonic obstruction, etc.)
  4. SCI and able-bodied patients who have a contraindication for OSPS (i.e., those with poor renal function, class 2 or greater symptomatic heart failure, ascites)
  5. SCI and able-bodied patients with a history of bradyarrhythmia, active coronary artery disease or asthma will also be excluded from receiving neostigmine/glycopyrrolate
  6. Known hypersensitivity to neostigmine or glycopyrrolate
  7. Potential for pregnancy. Women who are sexually active and of childbearing potential (i.e. not surgically sterile or at least 2 years postmenopausal) must have negative serum pregnancy test.)
  8. Lactating/nursing females
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00745095

Contacts
Contact: Robert E Williams     (718) 584-9000 ext 3126     robert.williams206485@va.gov    
Contact: Racine R Emmons     (718) 584-9000 ext 5246     racine.emmons@va.gov    

Locations
United States, New York
VA Medical Center, Bronx    
      Bronx, New York, United States, 10468

Sponsors and Collaborators

Investigators
Principal Investigator:     Mark A. Korsten, MD     VA Medical Center, Bronx    
  More Information


Responsible Party:   Department of Veterans Affairs ( Korsten, Mark - Principal Investigator )
Study ID Numbers:   A6428R
First Received:   September 2, 2008
Last Updated:   September 2, 2008
ClinicalTrials.gov Identifier:   NCT00745095
Health Authority:   United States: Federal Government;   United States: Food and Drug Administration

Keywords provided by Department of Veterans Affairs:
Safety  
Efficacy  
Colonoscopy  

Study placed in the following topic categories:
Spinal Cord Injuries
Neostigmine
Spinal Cord Diseases
Wounds and Injuries
Disorders of Environmental Origin
Central Nervous System Diseases
Trauma, Nervous System

Additional relevant MeSH terms:
Parasympathomimetics
Cholinesterase Inhibitors
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Autonomic Agents
Physiological Effects of Drugs
Nervous System Diseases
Enzyme Inhibitors
Peripheral Nervous System Agents
Cholinergic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 24, 2008




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