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WithdrawnNCT02574611Updated Sep 28, 2021

Use of High Resolution Colonic Manometry in Studying Motility

A Phase 1 interventional study of Neostigmine and Glycopyrrolate in Gastrointestinal Dysfunction, sponsored by James J. Peters Veterans Affairs Medical Center. Withdrawn at 1 site in United States. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-09-28.

Sponsored by James J. Peters Veterans Affairs Medical Center · Phase 1, Interventional, and Other

Why this study was withdrawn
No reportable findings are possible. The PI/Co-PI were unable to recruit participants for this study. One participant was consented but did not undergo any study procedure.
Phase
Phase 1
Study type
Interventional
Enrollment
0
Allocation
Non-randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

An injury to the spinal cord (SCI) results in numerous medical complications, including gastrointestinal (GI) function. Individuals with SCI may experience severe constipation (prolonged stool retention), incontinence (accidents), and overall difficulty in bowel evacuation. While various treatments and medications have been established to address this complication, there is little knowledge relating to the overall colonic motility. However, new technology such as High Resolution Colonic Manometry allows physicians to visualize high pressure contractions inside the colon, leading to a greater understanding of typical motility, a more accurate diagnosis, and an effective treatment. In this study, the investigators propose to use this technology to understand the effects of SCI on colonic motility by comparing to normal colonic function observed in able-bodied (AB) individuals. In addition, the investigators plan to study the effects of pharmacological treatments, such as neostigmine, on promoting peristaltic contractions in the colon as it is delivered across the skin.

Read the detailed description

The investigators data suggests that the fundamental consequence of SCI is a slowing of intestinal peristaltic activity, most likely as a result of down regulation of parasympathetic neural pathways. Furthermore, the investigators have effectively shown that measures involved in increase parasympathetic stimulation results in efficient bowel evacuation and improved bowel care. Such measures include the administration of neostigmine (NEO), which increases peristaltic contractions in the colon, resulting in predictable bowel evacuations. Given the cardiopulmonary side-effects of NEO, an ant-cholinergic known as Glycopyrrolate (GLY) is usually co-administered with NEO to reverse these side effects. However, the investigators knowledge regarding the effects of SCI on colonic motility is still primitive, mainly due to pervious technological disadvantages. New High Resolution Colonic Manometry systems (Medical Measurement Systems Dover, NH) simultaneously capture high amplitude pressure contractions (HAPCs) across the ascending, transverse, descending, and recto-sigmoid colon. Such capabilities allow for a much clearer display of pressure events compared to previous line tracing manometric systems and the direction of contractions are much easier to discern as well. To date, this technology has been an effective tool in diagnosing bowel disorders and complications, such as constipation in able-bodied individuals (AB). However, such studies have not been conducted in a SCI population. This technology also has the potential to capture the effects of NEO+GLY on improving colonic function.

02

Conditions studied

  • Gastrointestinal Dysfunction
03

In context

Lead sponsor

James J. Peters Veterans Affairs Medical Center is the lead sponsor of 49 studies on the registry; 4 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 2 (25%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Chronic SCI >1year
  • Able-Bodied (non SCI)
  • Undergoing Elective Colonoscopy
  • Age 18-75 years.

Exclusion criteria

Exclusion Criteria:

  • Previous adverse reaction or hypersensitivity to electrical stimulation
  • Known sensitivity to neostigmine or glycopyrrolate
  • Persons with SCI who do not require additional bowel care or have "normal bowel function"
  • Known hypersensitivity to neostigmine or glycopyrrolate
  • History of mechanical obstruction of the intestine or urinary tract
  • History of Myocardial infarction
  • Uncontrollable Hypertension Defined by a blood pressure reading of 160/100 mmHg or higher
  • Organ damage (heart \& kidney) and/or transient ischemic attack-cerebral vascular accident as a result of hypertension
  • Known past history of coronary artery disease or bradyarrythmia
  • Active respiratory disease
  • Known history of asthma during lifetime or recent (within 3 months) respiratory infections
  • Adrenal insufficiency
  • Diagnosed coagulopathy
  • Any renal disease or dysfunction
  • Potential for pregnancy
  • Lactating/nursing females
  • Slow-heart beat (HR\<45 bpm)
  • Lack of mental capacity to give consent
  • Use of any antibiotic in the past 7 days
  • Use of medications known to affect the respiratory system
  • Use of medications known to alter airway caliber
  • Concurrent participation in other clinical trials (within 30 days)
05

Study design

Phase
Phase 1
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Single group
Masking
Single (Participant)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    SCI observational

    Individuals with SCI will undergo a one day observation following elective colonoscopy and placement of the colonic catheter. Investigators will be monitoring colonic motility during a "typical" day (eating, sleeping, mobility, etc.).

    Device: High Resolution Colonic Manometry

  • Experimental
    Able-bodied observational

    Able-bodied individuals (non SCI) will undergo a one day observation following elective colonoscopy and placement of the colonic catheter. Investigators will be monitoring colonic motility during a "typical" day (eating, sleeping, mobility, etc.).

    Device: High Resolution Colonic Manometry

  • Active comparator
    SCI drug group

    Individuals with SCI will undergo a second day observation following elective colonoscopy and placement of the colonic catheter. Investigators will be monitoring colonic motility during the transdermal administration of neostigmine and glycopyrrolate.

    Drug: Neostigmine · Drug: Glycopyrrolate · Device: High Resolution Colonic Manometry

  • Placebo comparator
    SCI placebo group

    Individuals with SCI will undergo a second day of observation following elective colonoscopy and placement of the colonic catheter. Investigators will be monitoring colonic motility during the transdermal administration of normal saline solution (placebo).

    Other: Saline (Placebo) · Device: High Resolution Colonic Manometry

Interventions

  • DrugNeostigmine
  • DrugGlycopyrrolate
  • OtherSaline (Placebo)
  • DeviceHigh Resolution Colonic Manometry
06

What researchers measure

Primary outcomes

  1. High Amplitude Contractions

    Monitor changes in High Amplitude Contractions inside the colon during a typical day for SCI and AB patients. The manometry system will record these changes and allow the investigators to visualize changes during various activities (eating, resting, supine, seated, walking, etc.) The investigators will also measure changes in contractions during administration of prokinetic agents to promote bowel evacuations

    Time frame: 1-2days

07

Study locations

1 site
  • James J. Peters VA Medical Center
    Bronx, New York 10468, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02574611
Lead sponsor
James J. Peters Veterans Affairs Medical Center
Responsible party
Dr. Mark Korsten (Chief Gastroenterologist, James J. Peters Veterans Affairs Medical Center) — Principal investigator
First posted
Oct 14, 2015
Start date
Oct 13, 2015
Primary completion
Dec 25, 2017
Completion
Dec 25, 2018
Last update
Sep 28, 2021

Study contacts

Mark Korsten, MD
principal investigator · James J. Peters Veterans Affairs Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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