Crohn'sPhase 4NCT02465385
Single-dose Linaclotide for Capsule Endoscopy Preparation
A Phase 4 study testing Linaclotide in people with Crohn's and Ulcerative Colitis, run by University of Virginia at 1 site in United States.
Trial summary
Video capsule endoscopy is an important procedure that can be used by doctors to find abnormalities in the small intestine, especially those that can cause bleeding. The procedure uses a tiny wireless camera to take pictures of the digestive tract. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Crohn's, Ulcerative Colitis, Gastrointestinal Bleeding
- What is being tested?
- Linaclotide
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteUnited States
- Study dates
- Feb 2015to Jun 2016
- Phase
- Phase 4
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Schedule for video endoscopy at UVHS
- Ability to speak, read and write English
- Age >18
- Able to provide consent
Who cannot join
- Prisoner
- Woman who is currently pregnant or breastfeeding
- Allergy to linaclotide
- Patients with known or suspected mechanical gastrointestinal obstruction
Trial locations and contacts
1 site in 1 country.
United States1 site
University of Virginia Health System
Charlottesville, Virginia, 22903
About this study
Video capsule endoscopy is an important procedure that can be used by doctors to find abnormalities in the small intestine, especially those that can cause bleeding. The procedure uses a tiny wireless camera to take pictures of the digestive tract. The camera sits inside a vitamin-sized capsule that a person can swallow. As the capsule travels through the digestive tract, the camera takes thousands of pictures that are transmitted to a recorder worn on a belt around a person's waist or over his/her shoulder. However, abnormalities can be missed partly because the normal dark liquids present in the intestine can prevent abnormalities from being recorded, hiding them from the physician who reviews the video.
The current method used to clear these dark liquids from your small intestine is to follow a clear liquid diet and drink approximately 2 quarts of polyethylene glycol (Golytely®) the day before the video endoscopy and take simethicone (a medication used to treat symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating) the morning of the test.
Read more
Some of the current preparations to clear these dark liquids are not able to entirely prevent abnormalities from being missed and most have an unpleasant taste or involve drinking a lot of fluid.
Linaclotide (Linzess®) is a medication approved by the Food and Drug Administration (FDA) for the treatment of constipation and irritable bowel syndrome. It is not approved by the FDA for use as an aid for clearing dark liquid from the small intestine prior to a video endoscopy.
A recent presentation at a medical meeting proposed using one-dose of linaclotide (Linzess®) to improve cleansing of the small intestine for capsule endoscopy preparation to supplement fasting and clear liquid diet.
This report claimed a noticeably better quality of small intestine cleansing and a 20% shorter transit time for the capsule by taking one dose of linaclotide one hour before patients swallowed the video capsule.
The purpose of this study is to assess the use of one dose of linaclotide in terms of the total time it takes the capsule to move through the small bowel, and image quality as compared to the current method. The results of this study will be compared to previous patients who drank the preparation that is currently used
Read the detailed description
Video capsule endoscopy is an important modality for detection of lesions in the small intestine. It is particularly helpful in patients with occult sources of gastrointestinal bleeding, suspected Crohn's disease, ulcerative jejunitis, and in cases where a small intestinal neoplasm is suspected. Despite advances in technique and equipment, significant limitations remain in obtaining adequate visualization due to dark bilious fluid that obscures the mucosa. Furthermore, limitations of battery technology mean that in approximately 16.5% of studies the capsule will fail to visualize the entire small bowel. Numerous methods of bowel preparation have been used for capsule endoscopy. To date, all of them are unpleasant/have significant side effects. This is particularly onerous given that the majority has already had a similar but more extensive preparation for colonoscopy. Furthermore, overall efficacy is varied, and the preparation frequently remains suboptimal. The University of Virginia Health System Motility Lab uses a current regimen of 2000 mL of golytely and simethicone, but incomplete and partially occluded portions of the small bowel remain persistent clinical issues. Nearly one in five studies may ultimately have to be repeated as a result.
A recent presentation by Ira J. Schmelkin, M.D. proposed the use of single-dose linaclotide for capsule endoscopy preparation to supplement fasting and clear liquid diet. In an uncontrolled series, he noted a clinically significant improvement in preparation quality and a 20% shorter transit time (compared with published norms) with one higher range dose of linaclotide an hour prior to endoscopy. Linaclotide is guanylate cyclase-C that acts on the luminal surface of the intestinal epithelium thereby stimulating secretion of chloride and bicarbonate into the intestinal lumen, resulting in increased intestinal fluid and increased motility. The increased motility and secretion throughout the gastrointestinal tract make it a potentially useful agent to decrease capsule transit time and decrease the amount of dark small intestine fluid, thereby improving capsule endoscopy yield. Initial reports suggest that linoclotide is generally well tolerated, with the primary side effect of diarrhea. The investigators propose to study the use of a single dose for capsule endoscopy preparation.
The hypothesis is that single-dose linaclotide will lead to significantly decreased transit time and improved small bowel visualization quality when compared to controls using polyethylene glycol and simethicone (standard of care).
The investigators propose to prospectively enroll approximately 30 patients as subjects, who will receive a single dose of 290mcg one hour prior to capsule endoscopy. This was calculated using power calculations from values of the Viazis study, who noted an average transit time of approximately 290 minutes, compared with approximately 190 minutes in the data from Schmelkin. Given the standard deviation of approximately 90 minutes in Viazis, power calculation with an alpha of 0.05 and a beta of 0.80 would require 18 subjects per group. The investigators will target 30 to allow for dropouts and to allow the use of statistics pertaining to large (approximately 30 and up) numbers of subjects.
All adult patients undergoing capsule endoscopy (with the exception of certain criteria, such as severe gastroparesis, pregnancy, non-English speaking, prisoners, those unable to give consent, prior small intestinal resection) will be approached sequentially until completion of the study. These will be matched 1:1 with historic controls selected at random from cases in the prior three years. The same exclusion criteria will be applied to both groups. There will be two primary outcomes: total transit time and rated overall mucosal visualization (categorized as ideal, good, inadequate or poor/needs repetition). Primary analysis will presume no confounding and use a t-test and chi-square, respectively. Should the groups prove significantly different, the investigators also plan to use adjusted analysis. The investigators will plan to collect BMI, history of reflux, age, sex, gastroparesis, diabetes, narcotic use, other conditions e.g. Parkinson's, lupus, scleroderma as these may affect transit time for the historic controls.
Two gastrointestinal fellows or attending level gastroenterologists will perform the scoring of the images recorded during the capsule endoscopy in a blinded manner. Secondarily, the investigators will also look at the percentage of capsule endoscopies detecting a culprit lesion, and the percentage of failed (incomplete) studies.
- Conditions
- Crohn's, Ulcerative Colitis, Gastrointestinal Bleeding
- Being tested
- Linaclotide
- Medical subject headings
- Colitis, Ulcerative, Gastrointestinal Hemorrhage
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
LinaclotideDrug
Also called Linzess
Every participant with be given 290 mcg of linaclotide 1 hour prior to receiving their capsule, in place of the standard (golytely) preparation
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Linaclotide 290mcg Receives: Drug: Linaclotide |
What is being measured
The primary outcome is the main question the study is designed to answer.
Small bowel transit time
The time of transit will be reviewed on the following day after the study. The data is collected when the capsule is finished recording, approximately 10 hours post-dose
Measured: 10 hours post-dose
Secondary outcomes (1)
Overall mucosal visualization on the recorded images as rated by an expert reviewer and graded on a 5-point likert scale.
The mucosal visualization will be reviewed on the following day after the study. The data is collected when the capsule is finished recording, approximately 10 hours post-dose
Measured: 10 hours post-dose
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Jun 2015 (estimated)
- Study startFeb 2015
- Primary completionJun 2016
- Study completionJun 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Crohn'sStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Virginia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, R. Ann Hays, MD, University of Virginia
- Investigators
- Rachel Hays, MD, Principal investigator, Assistant professor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02465385
- Sponsor's protocol ID
- 17803
- Status last verified
- Jul 2016
- First submitted
- 27 May 2015
- Last updated
- 14 Jul 2016
- Results posted
- No
- Data monitoring committee
- No
Publications
Stein DJ, Copland A, McDaniel D, Hays RA. Single-Dose Linaclotide Is Equal in Efficacy to Polyethylene Glycol for Bowel Preparation Prior to Capsule Endoscopy. Dig Dis. 2019;37(4):297-302. doi: 10.1159/000496350. Epub 2019 Feb 7.
PubMed 30731474
Study at a glance
From the registry record, last updated by the sponsor on 14 Jul 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Single-dose Linaclotide for Capsule Endoscopy Preparation
- ClinicalTrials.gov ID
- NCT02465385
- Acronym / sponsor ID
- 17803
- Conditions
- Crohn's, Ulcerative Colitis, Gastrointestinal Bleeding
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- University of VirginiaUniversity, hospital or other
- Study start
- Feb 2015
- Primary completion
- Jun 2016 (actual)
- Study completion
- Jun 2016 (actual)
- First posted
- 8 Jun 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Video capsule endoscopy is an important procedure that can be used by doctors to find abnormalities in the small intestine, especially those that can cause bleeding. The procedure uses a tiny wireless camera to take pictures of the digestive tract. The camera sits inside a vitamin-sized capsule that a person can swallow. As the capsule travels through the digestive tract, the camera takes thousands of pictures that are transmitted to a recorder worn on a belt around a person's waist or over his/her shoulder. However, abnormalities can be missed partly because the normal dark liquids present in the intestine can prevent abnormalities from being recorded, hiding them from the physician who reviews the video.
The current method used to clear these dark liquids from your small intestine is to follow a clear liquid diet and drink approximately 2 quarts of polyethylene glycol (Golytely®) the day before the video endoscopy and take simethicone (a medication used to treat symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating) the morning of the test.
Some of the current preparations to clear these dark liquids are not able to entirely prevent abnormalities from being missed and most have an unpleasant taste or involve drinking a lot of fluid.
Linaclotide (Linzess®) is a medication approved by the Food and Drug Administration (FDA) for the treatment of constipation and irritable bowel syndrome. It is not approved by the FDA for use as an aid for clearing dark liquid from the small intestine prior to a video endoscopy.
A recent presentation at a medical meeting proposed using one-dose of linaclotide (Linzess®) to improve cleansing of the small intestine for capsule endoscopy preparation to supplement fasting and clear liquid diet.
This report claimed a noticeably better quality of small intestine cleansing and a 20% shorter transit time for the capsule by taking one dose of linaclotide one hour before patients swallowed the video capsule.
The purpose of this study is to assess the use of one dose of linaclotide in terms of the total time it takes the capsule to move through the small bowel, and image quality as compared to the current method. The results of this study will be compared to previous patients who drank the preparation that is currently used
Detailed description
Video capsule endoscopy is an important modality for detection of lesions in the small intestine. It is particularly helpful in patients with occult sources of gastrointestinal bleeding, suspected Crohn's disease, ulcerative jejunitis, and in cases where a small intestinal neoplasm is suspected. Despite advances in technique and equipment, significant limitations remain in obtaining adequate visualization due to dark bilious fluid that obscures the mucosa. Furthermore, limitations of battery technology mean that in approximately 16.5% of studies the capsule will fail to visualize the entire small bowel. Numerous methods of bowel preparation have been used for capsule endoscopy. To date, all of them are unpleasant/have significant side effects. This is particularly onerous given that the majority has already had a similar but more extensive preparation for colonoscopy. Furthermore, overall efficacy is varied, and the preparation frequently remains suboptimal. The University of Virginia Health System Motility Lab uses a current regimen of 2000 mL of golytely and simethicone, but incomplete and partially occluded portions of the small bowel remain persistent clinical issues. Nearly one in five studies may ultimately have to be repeated as a result.
A recent presentation by Ira J. Schmelkin, M.D. proposed the use of single-dose linaclotide for capsule endoscopy preparation to supplement fasting and clear liquid diet. In an uncontrolled series, he noted a clinically significant improvement in preparation quality and a 20% shorter transit time (compared with published norms) with one higher range dose of linaclotide an hour prior to endoscopy. Linaclotide is guanylate cyclase-C that acts on the luminal surface of the intestinal epithelium thereby stimulating secretion of chloride and bicarbonate into the intestinal lumen, resulting in increased intestinal fluid and increased motility. The increased motility and secretion throughout the gastrointestinal tract make it a potentially useful agent to decrease capsule transit time and decrease the amount of dark small intestine fluid, thereby improving capsule endoscopy yield. Initial reports suggest that linoclotide is generally well tolerated, with the primary side effect of diarrhea. The investigators propose to study the use of a single dose for capsule endoscopy preparation.
The hypothesis is that single-dose linaclotide will lead to significantly decreased transit time and improved small bowel visualization quality when compared to controls using polyethylene glycol and simethicone (standard of care).
The investigators propose to prospectively enroll approximately 30 patients as subjects, who will receive a single dose of 290mcg one hour prior to capsule endoscopy. This was calculated using power calculations from values of the Viazis study, who noted an average transit time of approximately 290 minutes, compared with approximately 190 minutes in the data from Schmelkin. Given the standard deviation of approximately 90 minutes in Viazis, power calculation with an alpha of 0.05 and a beta of 0.80 would require 18 subjects per group. The investigators will target 30 to allow for dropouts and to allow the use of statistics pertaining to large (approximately 30 and up) numbers of subjects.
All adult patients undergoing capsule endoscopy (with the exception of certain criteria, such as severe gastroparesis, pregnancy, non-English speaking, prisoners, those unable to give consent, prior small intestinal resection) will be approached sequentially until completion of the study. These will be matched 1:1 with historic controls selected at random from cases in the prior three years. The same exclusion criteria will be applied to both groups. There will be two primary outcomes: total transit time and rated overall mucosal visualization (categorized as ideal, good, inadequate or poor/needs repetition). Primary analysis will presume no confounding and use a t-test and chi-square, respectively. Should the groups prove significantly different, the investigators also plan to use adjusted analysis. The investigators will plan to collect BMI, history of reflux, age, sex, gastroparesis, diabetes, narcotic use, other conditions e.g. Parkinson's, lupus, scleroderma as these may affect transit time for the historic controls.
Two gastrointestinal fellows or attending level gastroenterologists will perform the scoring of the images recorded during the capsule endoscopy in a blinded manner. Secondarily, the investigators will also look at the percentage of capsule endoscopies detecting a culprit lesion, and the percentage of failed (incomplete) studies.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Drug: LinaclotideLinaclotide 290mcg |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Schedule for video endoscopy at UVHS
- Ability to speak, read and write English
- Age >18
- Able to provide consent
Key exclusion criteria (4 listed)
- Prisoner
- Woman who is currently pregnant or breastfeeding
- Allergy to linaclotide
- Patients with known or suspected mechanical gastrointestinal obstruction
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| LinaclotideAlso: LinzessEvery participant with be given 290 mcg of linaclotide 1 hour prior to receiving their capsule, in place of the standard (golytely) preparation | Drug | Intervention |
Primary outcome
Small bowel transit time
Time frame: 10 hours post-dose
The time of transit will be reviewed on the following day after the study. The data is collected when the capsule is finished recording, approximately 10 hours post-dose
1 secondary outcome
Overall mucosal visualization on the recorded images as rated by an expert reviewer and graded on a 5-point likert scale.
Time frame: 10 hours post-dose
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jul 2016.
- Derived from this study: PubMed 30731474Stein DJ, Copland A, McDaniel D, Hays RA. Single-Dose Linaclotide Is Equal in Efficacy to Polyethylene Glycol for Bowel Preparation Prior to Capsule Endoscopy. Dig Dis. 2019;37(4):297-302. doi: 10.1159/000496350. Epub 2019 Feb 7.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rachel Hays, MD principal investigator
Assistant professor
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Linaclotide in people with Crohn's and Ulcerative Colitis, run by University of Virginia at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Jul 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Small bowel transit time (time frame: 10 hours post-dose). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02465385, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jul 2016.