Use of Prokinetics During Inpatient Bowel Care for SCI Patients
| Status: | Recruiting |
|---|---|
| Conditions: | Hospital, Orthopedic |
| Therapuetic Areas: | Orthopedics / Podiatry, Other |
| Healthy: | No |
| Age Range: | 18 - 75 |
| Updated: | 8/30/2017 |
| Start Date: | December 2012 |
| End Date: | December 2018 |
| Contact: | Mark A Korsten, MD |
| Email: | mark.korsten@va.gov |
| Phone: | 718-584-9000 |
Bowel care (BC) is a time-consuming and cumbersome activity of daily living for most
individuals with SCI. Previous studies have reported that the average time to complete a BC
routine is 45 minutes; 10-20% of SCI individuals report BC routines lasting for more than 1
hour. In past studies, the investigators have shown that a medication called neostigmine can
increase bowel activity and thus, promote bowel movement. The investigators have successfully
used this medication with traditional and novel methods of colonoscopic preparations, and
have shown that it improves the quality of these preparations. In this study, we would like
to test the applicability of this medication to bowel care routines.
The investigators believe that the addition of this medication to the beginning of regular
bowel regiments will significantly decrease the time and effort needed to complete BC, thus
improving patient perception of their BC routines and quality of life. SCI individuals
followed by the James J Peters VA Medical Center (JJPVAMC) SCI Medical Service are admitted
on a routine basis for inpatient respite care, therapy, and/or annual physicals. Such
inpatient stays typically range in duration from 1 week to 3 weeks, during which the patient
undergo BC routines assisted by the inpatient care team. BC routines are typically performed
every other day, or thrice weekly (Monday, Wednesday, Friday) in "Blue Rooms" located on the
inpatient SCI wards (IE and ID). The bowel care routine, including duration of procedure, use
of assistive medications or devices, and completeness of bowel care are documented in the
patients' electronic medical chart (CPRS) by care providers. The investigators propose to
perform the described protocol in individuals who have been admitted to the hospital for
routine care and are otherwise healthy. In doing so, the investigators can ensure that
patients are vigilantly monitored during each BC session, and that any changes in BC pattern
are accurately observed and documented. Furthermore, by performing these procedures on an
inpatient basis, study investigators can ensure the consistency of care and daily routine,
allowing for better control of study conditions.
individuals with SCI. Previous studies have reported that the average time to complete a BC
routine is 45 minutes; 10-20% of SCI individuals report BC routines lasting for more than 1
hour. In past studies, the investigators have shown that a medication called neostigmine can
increase bowel activity and thus, promote bowel movement. The investigators have successfully
used this medication with traditional and novel methods of colonoscopic preparations, and
have shown that it improves the quality of these preparations. In this study, we would like
to test the applicability of this medication to bowel care routines.
The investigators believe that the addition of this medication to the beginning of regular
bowel regiments will significantly decrease the time and effort needed to complete BC, thus
improving patient perception of their BC routines and quality of life. SCI individuals
followed by the James J Peters VA Medical Center (JJPVAMC) SCI Medical Service are admitted
on a routine basis for inpatient respite care, therapy, and/or annual physicals. Such
inpatient stays typically range in duration from 1 week to 3 weeks, during which the patient
undergo BC routines assisted by the inpatient care team. BC routines are typically performed
every other day, or thrice weekly (Monday, Wednesday, Friday) in "Blue Rooms" located on the
inpatient SCI wards (IE and ID). The bowel care routine, including duration of procedure, use
of assistive medications or devices, and completeness of bowel care are documented in the
patients' electronic medical chart (CPRS) by care providers. The investigators propose to
perform the described protocol in individuals who have been admitted to the hospital for
routine care and are otherwise healthy. In doing so, the investigators can ensure that
patients are vigilantly monitored during each BC session, and that any changes in BC pattern
are accurately observed and documented. Furthermore, by performing these procedures on an
inpatient basis, study investigators can ensure the consistency of care and daily routine,
allowing for better control of study conditions.
Part 1: IV Screening Twenty subjects with chronic SCI (>1 year) and difficulty with
evacuation (DWE) managed by a regular, thrice weekly BC routines will be recruited for study
participation. In order to determine eligibility for the study, the subject will have to
undergo an IV screening to test whether or not they are responsive to the drug treatment
(neostigmine-glycopyrrolate). If the subject responds (bowel movement) to the IV treatment,
they will be allowed to continue on to part 2 of the study. If patient does not have a
successful bowel movement, then they will be considered a non-responder and study
participation will be discontinued.
Part 2: Baseline and Dose Titration Once eligibility has been determined, and subject consent
has been obtained, each subject will undergo 1 week of baseline observation after admission.
An abdominal x-ray (KUB) will be performed, the SCI Bowel Survey and Treatment Satisfaction
Questionnaire (TSQM) will be administered, and the subject's weight determined. Each subject
will continue with regular bowel care as an inpatient, and after 1 week, all of the baseline
measurements (KUB, weight and surveys) will be repeated. This will be followed by a 2 visit-
dose titration study of concomitantly administered, transcutaneous neostigmine methylsulfate
(NEO) and glycopyrrolate (GLY). Each visit will be scheduled on a BC day. All procedures will
take place in the "Blue Room" located in the SCI inpatient ward. Subjects will be prone
throughout the duration of the study, in a stretcher routinely used during bowel care. As
part of the setup, subjects will be instrumented with blood pressure cuff; intravenous access
will be obtained at a peripheral vein (if one is not available), as a precautionary measure,
since the drug will be administered via an Iontophoresis transdermal patch. Heart rate will
be continuously monitored throughout the procedure through finger oximetry. Symptoms will be
assessed every 5 minutes for the first 30 minutes, and then at 1 hour post drug
administration. Once the subject has a positive response to one of the two doses, or the
higher dose has been performed, the dose titration will be stopped. If the subject has a
positive response (bowel movement within 60 minutes of drug administration) he/she will be
eligible to continue to the third study phase. If the subject does not respond to either
dose, the subject will be considered a non-responder and study participation will be
discontinued. We expect that about 1/3rd of the subjects will be non-responders, or will be
lost to attrition; therefore, we are prepared to over-recruit by 5 subjects in order to
ensure that at least 15 subjects will be eligible to complete the second part of the study.
The study will be stopped once the patient experiences a bowel movement within 30 minutes of
administering ION NEO because the protocol objective will have been achieved. If the patient
should experience cardiopulmonary side effects when receiving the ION NEO on the lower doses
that are not effectively reversed by the ION GLY, the study will be stopped. In addition, the
study investigators reserve the right to stop the study should they have any other safety
concerns.
Part 3: 2 Week Treatment Each subject will be assessed for their perception of their current
BC routine using the Treatment Satisfaction Questionnaire for Medication (TSQM-Appendix 1),
and their bowel habits using the bowel survey (Appendix 2).The subject will then be asked to
continue with their normal BC routine for two weeks during their inpatient stay, with the
exception that NEO and GLY will be administered at the beginning of each BC session as an
adjunct to each subject's normal routine. Each BC session will be documented by a study team
member including the time needed to complete BC, methods used (i.e. number of enemas used,
oral laxatives, suppositories, digital stimulation, abdominal massage) and the quality and
completeness of the bowel movement. Heart rate, oxygenation and blood pressure will be
monitored continuously. Subjects will be weighed at baseline, once after each week of
treatment and once at the post treatment follow-up visit. After two weeks of treatment, each
subject will undergo a final KUB and be reassessed for their perception of the BC routine for
the past two weeks using the TSQM and their bowel habits (bowel survey).
evacuation (DWE) managed by a regular, thrice weekly BC routines will be recruited for study
participation. In order to determine eligibility for the study, the subject will have to
undergo an IV screening to test whether or not they are responsive to the drug treatment
(neostigmine-glycopyrrolate). If the subject responds (bowel movement) to the IV treatment,
they will be allowed to continue on to part 2 of the study. If patient does not have a
successful bowel movement, then they will be considered a non-responder and study
participation will be discontinued.
Part 2: Baseline and Dose Titration Once eligibility has been determined, and subject consent
has been obtained, each subject will undergo 1 week of baseline observation after admission.
An abdominal x-ray (KUB) will be performed, the SCI Bowel Survey and Treatment Satisfaction
Questionnaire (TSQM) will be administered, and the subject's weight determined. Each subject
will continue with regular bowel care as an inpatient, and after 1 week, all of the baseline
measurements (KUB, weight and surveys) will be repeated. This will be followed by a 2 visit-
dose titration study of concomitantly administered, transcutaneous neostigmine methylsulfate
(NEO) and glycopyrrolate (GLY). Each visit will be scheduled on a BC day. All procedures will
take place in the "Blue Room" located in the SCI inpatient ward. Subjects will be prone
throughout the duration of the study, in a stretcher routinely used during bowel care. As
part of the setup, subjects will be instrumented with blood pressure cuff; intravenous access
will be obtained at a peripheral vein (if one is not available), as a precautionary measure,
since the drug will be administered via an Iontophoresis transdermal patch. Heart rate will
be continuously monitored throughout the procedure through finger oximetry. Symptoms will be
assessed every 5 minutes for the first 30 minutes, and then at 1 hour post drug
administration. Once the subject has a positive response to one of the two doses, or the
higher dose has been performed, the dose titration will be stopped. If the subject has a
positive response (bowel movement within 60 minutes of drug administration) he/she will be
eligible to continue to the third study phase. If the subject does not respond to either
dose, the subject will be considered a non-responder and study participation will be
discontinued. We expect that about 1/3rd of the subjects will be non-responders, or will be
lost to attrition; therefore, we are prepared to over-recruit by 5 subjects in order to
ensure that at least 15 subjects will be eligible to complete the second part of the study.
The study will be stopped once the patient experiences a bowel movement within 30 minutes of
administering ION NEO because the protocol objective will have been achieved. If the patient
should experience cardiopulmonary side effects when receiving the ION NEO on the lower doses
that are not effectively reversed by the ION GLY, the study will be stopped. In addition, the
study investigators reserve the right to stop the study should they have any other safety
concerns.
Part 3: 2 Week Treatment Each subject will be assessed for their perception of their current
BC routine using the Treatment Satisfaction Questionnaire for Medication (TSQM-Appendix 1),
and their bowel habits using the bowel survey (Appendix 2).The subject will then be asked to
continue with their normal BC routine for two weeks during their inpatient stay, with the
exception that NEO and GLY will be administered at the beginning of each BC session as an
adjunct to each subject's normal routine. Each BC session will be documented by a study team
member including the time needed to complete BC, methods used (i.e. number of enemas used,
oral laxatives, suppositories, digital stimulation, abdominal massage) and the quality and
completeness of the bowel movement. Heart rate, oxygenation and blood pressure will be
monitored continuously. Subjects will be weighed at baseline, once after each week of
treatment and once at the post treatment follow-up visit. After two weeks of treatment, each
subject will undergo a final KUB and be reassessed for their perception of the BC routine for
the past two weeks using the TSQM and their bowel habits (bowel survey).
Inclusion Criteria:
- Age: 18-75 years
- Spinal Cord Injury (SCI):
- greater than 1 year duration
- excess time for bowel evacuation (> 60minutes per session)
Exclusion Criteria:
- Previous Adverse Reaction or Hypersensitivity to Electrical Stimulation
- Do not require additional bowel care or have "normal bowel function"
- Known sensitivity to Neostigmine and Glycopyrrolate
- Blockage in Bowel and/or Bladder
- Myocardial Infarction in the past 6months
- Blood Pressure ≥160/100 mmHg with/without being on 3 or more different classes of
antihypertensive medications
- Organ Damage (heart & kidney) and/or transient ischemic attack (TIA)- cerebrovascular
accident (CVA) as a result of hypertension
- Known past history of coronary artery disease, chronic heart failure, bradyarrythmia
- Slow Heart Rate (<45bpm)
- Active respiratory diseases
- Known history of asthma during lifetime
- Recent (within 3months) respiratory infections
- Adrenal Insufficiency
- Pregnancy or potential for pregnancy
- Lactating/nursing females
- Use of any antibiotics in past 7days
- Use of medications known to affect respiratory system
- Concurrent participation in other clinical trials (within 30days)
We found this trial at
1
site
130 West Kingsbridge Road
The Bronx, New York 10468
The Bronx, New York 10468
Principal Investigator: Mark A. Korsten, MD
Phone: 718-584-9000
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