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Use of Pyridostigmine for Constipation in Diabetics

Primary Purpose

Constipation, Diabetes Mellitus, Colonic Transit

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Pyridostigmine
Placebo
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Constipation

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects with diabetes mellitus (Type I or type II), diagnosed by a physician. On medical treatment for diabetes (oral medication or injected insulin) for at least one year Symptomatic constipation at least 25% of the time in the past year (Rome II criteria for functional constipation) 18-70 years of age Colonoscopy negative for obstructive lesions, cancer, or inflammatory bowel disease (IBS) within the last 8 years if 50 years of age or older Able to provide written informed consent before participating in trial Able to communicate adequately with the Investigator and to comply with the requirements for the entire study Exclusion Criteria: History of pelvic floor dysfunction (other functional GI disorders, eg IBS, non-ulcer dyspepsia are acceptable); Specifically, patients will be excluded if they have at least 2 of the following 3 criteria: History of digital evacuation of the rectum or pressure on the posterior aspect of the vagina or perineum to facilitate defecation Examination findings suggestive of puborectalis spasm or anismus, on assessment by an experienced gastroenterologist with expertise in this field; i.e. high anal sphincter tone at rest, failure of perineal descent by >1cm on straining, and tenderness or paradoxical contraction of the puborectalis on digital examination Requirement of > 200g to expel a rectal balloon during voluntary straining Abdominal surgery other than appendectomy, cholecystectomy, hysterectomy, tubal ligation, or inguinal hernia repair Suspected or known gastrointestinal or genitourinary obstruction Uncontrolled hypertension (defined as > 150/90 at rest) Known cardiac arrhythmia or ECG abnormalities, i.e. cardiac conduction disturbances (2nd or 3rd degree atrioventricular (AV) block, prolonged corrected QT interval (QTc)(> 460 msec) or bradycardia (< 45 beats/minute)) Renal insufficiency with serum creatinine greater than 2 mg/dl based on a reading from the previous 6 months Asthma or chronic obstructive pulmonary disease requiring systemic steroids in the previous 3 years (inhaled steroids acceptable) Current use of narcotics, gut prokinetic drugs (eg metoclopramide, domperidone, tegaserod, senekot), anticholinergic medication (eg. Hyoscyamine, belladonna), antidiarrheals (Imodium, Lomotil), or laxatives other than fiber supplements, docusate, or glycerin suppositories. Patients on any of these restricted medications must cease use at least 48 hours before starting and for the duration of both study phases. No rescue laxatives will be permitted within 7 days of transit testing Patients who have taken any investigational medications within the past 30 days Known intolerance or allergy to eggs Pregnant or breast-feeding females

Sites / Locations

  • Mayo Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Pyridostigmine

Placebo

Arm Description

Oral pyridostigmine, starting with 60 mg capsules three times per day (TID), increasing by 60 mg every third day (i.e., over 10 days) up to the maximum tolerated dose or 120 mg TID (a total of 360 mg per day). This dose was maintained for 7 days.

Placebo (sham) capsules, matching the appearance of the active drug comparator and taken TID.

Outcomes

Primary Outcome Measures

Colonic Geometric Center at 24 Hours (GC24) Measured by Scintigraphy
The scintigraphic method is used to measure colonic transit. An isotope is adsorbed on activated charcoal particles and delivered to the colon in a delayed release capsule. Anterior and posterior gamma images of the abdomen are taken hourly for the first 6 hours after the radio-labeled meal, then at 8, 24 and 48 hours. The geometric center (GC) is the weighted average of counts in the different colonic regions. The scale ranges from 1 to 5; a high GC implies faster colonic transit, a GC of 1 implies all isotope is in the ascending colon, and a GC of 5 implies all isotope is in the stool. GC24 is the measurement taken at 24 hours after the radio-labeled meal.
Ascending Colon Emptying Half-time (AC t1/2) Measured in Hours
Calculated by linear interpolation of values on the AC emptying curve.

Secondary Outcome Measures

Gastric Emptying Half-time (GE t1/2)
The measure of time for 50 percent of a radio-labeled meal to empty from the stomach.
Colonic Filling at 6 Hours
The proportion of a radio-labeled meal in the colon at 6 hours (identifiable by radio-labelled tracer to capsule eaten with meal), measured by scintigraphy. This is an indirect measurement of small-bowel transit time.
Colonic Geometric Center at 48 Hours (GC48) as Measured by Scintigraphy
The scintigraphic method is used to measure colonic transit. An isotope is adsorbed on activated charcoal particles and delivered to the colon in a delayed release capsule. Anterior and posterior gamma images are taken hourly for the first 6 hours after the radio-labeled meal, then at 8, 24 and 48 hours. The geometric center (GC) is the weighted average of counts in the different colonic regions. The scale ranges from 1 to 5; a high GC implies faster colonic transit, a GC of 1 implies all isotope is in the ascending colon, and a GC of 5 implies all isotope is in the stool. GC48 is the measurement taken at 48 hours after the radio-labeled meal.
Stool Frequency Per Day
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record the number of times per day they had a bowel movement. Only the 7 days of highest treatment dose will be used for comparison purposes.
Stool Form/Consistency
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record a description of stool consistency according to the Bristol Stool Form Scale (ranging from 1 (hard lumps) to 7 (watery)). The Bristol Stool Scale is a medical aid designed to classify the form of human feces into seven categories or types. Types 1 and 2 indicate constipation with 3 and 4 being the "ideal stools" especially the latter, as they are the easiest to defecate, and 5-7 tending towards diarrhea.
Stool Ease of Passage
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record a description of stool ease of passage of stool, according to the Bristol Stool Form Scale (ranging from 1 (manual disimpaction) to 7 (incontinence)). Only the 7 days at highest treatment dose will be used for comparison purposes.
Sense of Completely Emptying Bowels
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record whether or not they felt they had completely emptied their bowels(1= Yes; 0= No). Only the 7 days of highest treatment dose will be used for comparison purposes.
Stool Frequency Per Week
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record the number of times per day they had a bowel movement. Complete spontaneous bowel movements per week are reported. Only the 7 days of highest treatment dose will be used for comparison purposes.
Heart Rate Before and After Treatment
Heart rate is the number of beats per minute, as recording on an Electrocardiogram (ECG).
QTc Interval Before and After Treatment
The corrected QT interval (QTc) is a measurement of time (seconds) between the Q and T waves of an heart beat as recorded during an Electrocardiogram (ECG).

Full Information

First Posted
January 11, 2006
Last Updated
November 2, 2012
Sponsor
Mayo Clinic
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Center for Research Resources (NCRR)
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1. Study Identification

Unique Protocol Identification Number
NCT00276406
Brief Title
Use of Pyridostigmine for Constipation in Diabetics
Official Title
Pyridostigmine in Diabetics With Constipation: Randomized, Placebo-controlled, Double-blind Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2012
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
October 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Center for Research Resources (NCRR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Doctors at Mayo Clinic are doing this study to learn if pyridostigmine, a drug, affects the speed at which food travels through the stomach, intestines and colon, and if pyridostigmine improves constipation symptoms in patients with diabetes. Pyridostigmine has been approved by the Food and Drug Administration (FDA) for routine clinical use, however, its use as proposed in this study is considered investigational.
Detailed Description
Chronic constipation in diabetes mellitus is associated with colonic motor dysfunction and is managed with laxatives. Cholinesterase inhibitors increase colonic motility. The study evaluated the effects of a cholinesterase inhibitor (pyridostigmine vs. placebo) on gastrointestinal and colonic transit and bowel function in diabetic patients with constipation. After a 9-day baseline period, patients with diabetes mellitus and chronic constipation without defecatory disorder will be randomized to oral placebo or pyridostigmine, starting with 60 mg three times a day, increasing by 60 mg every third day up to the maximum tolerated dose of 120 mg three times a day; this dose will be maintained for 7 days. Gastrointestinal and colonic transit (assessed by scintigraphy) and bowel function will be evaluated at baseline and the final 3 and 7 days of treatment, respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation, Diabetes Mellitus, Colonic Transit, Gastric Emptying

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pyridostigmine
Arm Type
Experimental
Arm Description
Oral pyridostigmine, starting with 60 mg capsules three times per day (TID), increasing by 60 mg every third day (i.e., over 10 days) up to the maximum tolerated dose or 120 mg TID (a total of 360 mg per day). This dose was maintained for 7 days.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo (sham) capsules, matching the appearance of the active drug comparator and taken TID.
Intervention Type
Drug
Intervention Name(s)
Pyridostigmine
Other Intervention Name(s)
Mestinon
Intervention Description
Pyridostigmine will be started at (60mg) tid, increased over 10 days to 120 mg tid, and maintained at that dose for 7 days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
If subject is randomized to placebo, placebo pills will be started at (60mg) tid, increased over 10 days to 120 mg tid, and maintained at that dose for 7 days.
Primary Outcome Measure Information:
Title
Colonic Geometric Center at 24 Hours (GC24) Measured by Scintigraphy
Description
The scintigraphic method is used to measure colonic transit. An isotope is adsorbed on activated charcoal particles and delivered to the colon in a delayed release capsule. Anterior and posterior gamma images of the abdomen are taken hourly for the first 6 hours after the radio-labeled meal, then at 8, 24 and 48 hours. The geometric center (GC) is the weighted average of counts in the different colonic regions. The scale ranges from 1 to 5; a high GC implies faster colonic transit, a GC of 1 implies all isotope is in the ascending colon, and a GC of 5 implies all isotope is in the stool. GC24 is the measurement taken at 24 hours after the radio-labeled meal.
Time Frame
Baseline period (days 7-9 ), Treatment period (days 14-17)
Title
Ascending Colon Emptying Half-time (AC t1/2) Measured in Hours
Description
Calculated by linear interpolation of values on the AC emptying curve.
Time Frame
Baseline period (days 7-9 ), Treatment period (days 14-17)
Secondary Outcome Measure Information:
Title
Gastric Emptying Half-time (GE t1/2)
Description
The measure of time for 50 percent of a radio-labeled meal to empty from the stomach.
Time Frame
Baseline period (9 days), Treatment period (7 days)
Title
Colonic Filling at 6 Hours
Description
The proportion of a radio-labeled meal in the colon at 6 hours (identifiable by radio-labelled tracer to capsule eaten with meal), measured by scintigraphy. This is an indirect measurement of small-bowel transit time.
Time Frame
Baseline period (9 days), Treatment period (7 days)
Title
Colonic Geometric Center at 48 Hours (GC48) as Measured by Scintigraphy
Description
The scintigraphic method is used to measure colonic transit. An isotope is adsorbed on activated charcoal particles and delivered to the colon in a delayed release capsule. Anterior and posterior gamma images are taken hourly for the first 6 hours after the radio-labeled meal, then at 8, 24 and 48 hours. The geometric center (GC) is the weighted average of counts in the different colonic regions. The scale ranges from 1 to 5; a high GC implies faster colonic transit, a GC of 1 implies all isotope is in the ascending colon, and a GC of 5 implies all isotope is in the stool. GC48 is the measurement taken at 48 hours after the radio-labeled meal.
Time Frame
Baseline period (days 7-9 ), Treatment period (days 14-17)
Title
Stool Frequency Per Day
Description
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record the number of times per day they had a bowel movement. Only the 7 days of highest treatment dose will be used for comparison purposes.
Time Frame
Daily during baseline period (9 days), Treatment period (7 days)
Title
Stool Form/Consistency
Description
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record a description of stool consistency according to the Bristol Stool Form Scale (ranging from 1 (hard lumps) to 7 (watery)). The Bristol Stool Scale is a medical aid designed to classify the form of human feces into seven categories or types. Types 1 and 2 indicate constipation with 3 and 4 being the "ideal stools" especially the latter, as they are the easiest to defecate, and 5-7 tending towards diarrhea.
Time Frame
Daily during baseline period (9 days), Treatment period (7 days)
Title
Stool Ease of Passage
Description
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record a description of stool ease of passage of stool, according to the Bristol Stool Form Scale (ranging from 1 (manual disimpaction) to 7 (incontinence)). Only the 7 days at highest treatment dose will be used for comparison purposes.
Time Frame
Daily during baseline period (9 days), Treatment period (7 days)
Title
Sense of Completely Emptying Bowels
Description
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record whether or not they felt they had completely emptied their bowels(1= Yes; 0= No). Only the 7 days of highest treatment dose will be used for comparison purposes.
Time Frame
Daily during baseline period (9 days), Treatment period (7 days)
Title
Stool Frequency Per Week
Description
During 9 days of the baseline period and during 17 days of the treatment period, subjects used a daily diary to record the number of times per day they had a bowel movement. Complete spontaneous bowel movements per week are reported. Only the 7 days of highest treatment dose will be used for comparison purposes.
Time Frame
Daily during baseline period (9 days), Treatment period (7 days)
Title
Heart Rate Before and After Treatment
Description
Heart rate is the number of beats per minute, as recording on an Electrocardiogram (ECG).
Time Frame
Baseline period (9 days), Treatment period (7 days)
Title
QTc Interval Before and After Treatment
Description
The corrected QT interval (QTc) is a measurement of time (seconds) between the Q and T waves of an heart beat as recorded during an Electrocardiogram (ECG).
Time Frame
Baseline period (9 days), Treatment period (7 days)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects with diabetes mellitus (Type I or type II), diagnosed by a physician. On medical treatment for diabetes (oral medication or injected insulin) for at least one year Symptomatic constipation at least 25% of the time in the past year (Rome II criteria for functional constipation) 18-70 years of age Colonoscopy negative for obstructive lesions, cancer, or inflammatory bowel disease (IBS) within the last 8 years if 50 years of age or older Able to provide written informed consent before participating in trial Able to communicate adequately with the Investigator and to comply with the requirements for the entire study Exclusion Criteria: History of pelvic floor dysfunction (other functional GI disorders, eg IBS, non-ulcer dyspepsia are acceptable); Specifically, patients will be excluded if they have at least 2 of the following 3 criteria: History of digital evacuation of the rectum or pressure on the posterior aspect of the vagina or perineum to facilitate defecation Examination findings suggestive of puborectalis spasm or anismus, on assessment by an experienced gastroenterologist with expertise in this field; i.e. high anal sphincter tone at rest, failure of perineal descent by >1cm on straining, and tenderness or paradoxical contraction of the puborectalis on digital examination Requirement of > 200g to expel a rectal balloon during voluntary straining Abdominal surgery other than appendectomy, cholecystectomy, hysterectomy, tubal ligation, or inguinal hernia repair Suspected or known gastrointestinal or genitourinary obstruction Uncontrolled hypertension (defined as > 150/90 at rest) Known cardiac arrhythmia or ECG abnormalities, i.e. cardiac conduction disturbances (2nd or 3rd degree atrioventricular (AV) block, prolonged corrected QT interval (QTc)(> 460 msec) or bradycardia (< 45 beats/minute)) Renal insufficiency with serum creatinine greater than 2 mg/dl based on a reading from the previous 6 months Asthma or chronic obstructive pulmonary disease requiring systemic steroids in the previous 3 years (inhaled steroids acceptable) Current use of narcotics, gut prokinetic drugs (eg metoclopramide, domperidone, tegaserod, senekot), anticholinergic medication (eg. Hyoscyamine, belladonna), antidiarrheals (Imodium, Lomotil), or laxatives other than fiber supplements, docusate, or glycerin suppositories. Patients on any of these restricted medications must cease use at least 48 hours before starting and for the duration of both study phases. No rescue laxatives will be permitted within 7 days of transit testing Patients who have taken any investigational medications within the past 30 days Known intolerance or allergy to eggs Pregnant or breast-feeding females
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adil E. Bharucha, MBBS, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22677718
Citation
Bharucha AE, Low P, Camilleri M, Veil E, Burton D, Kudva Y, Shah P, Gehrking T, Zinsmeister AR. A randomised controlled study of the effect of cholinesterase inhibition on colon function in patients with diabetes mellitus and constipation. Gut. 2013 May;62(5):708-15. doi: 10.1136/gutjnl-2012-302483. Epub 2012 Jun 7.
Results Reference
result
Links:
URL
http://clinicaltrials.mayo.edu
Description
Mayo Clinic Clinical Trials

Learn more about this trial

Use of Pyridostigmine for Constipation in Diabetics

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