A Pilot Study to Assess the Efficacy and Safety of Various Vibrating Capsule Modes
| Status: | Completed |
|---|---|
| Conditions: | Constipation |
| Therapuetic Areas: | Gastroenterology |
| Healthy: | No |
| Age Range: | 22 - Any |
| Updated: | 5/24/2018 |
| Start Date: | November 14, 2017 |
| End Date: | March 30, 2018 |
A Prospective, Multicenter, Randomized, Double-blind, Sham-controlled Pilot Study to Assess the Efficacy and Safety of Various Vibrating Capsule Modes
The study is a prospective, adaptive, multicenter, randomized, double-blind, Sham-controlled
pilot study, to evaluate the efficacy and safety of the Vibrant Capsule in relieving
constipation in subjects with functional constipation.
Three arms will be assessed:
- Vibrant Capsule with vibrating mode 1 administered 5 times per week
- Vibrant Capsule with vibrating mode 2 administered 5 times per week
- Sham Capsule administered 5 times per week
Subjects will be followed continuously for at least a 2 weeks run-in period and then be
randomized to either Vibrant or Sham capsules for a treatment period of 8 weeks. The first 2
weeks of treatment will be considered as a subjects' training period.
Data reporting will be done on an electronic Case Report Form and an eDiary. Subjects will be
asked to refrain from taking any medication or supplement to relieve their constipation,
during the entire study period.
After the run-in period, the subjects will return and eligibility will be re-assessed.
Subjects will be trained on how to use the base unit and will swallow the first capsule on
site the day of baseline visit. They will activate and ingest the rest of the capsules at
home by themselves, using the base unit.
Subjects will be instructed to complete a simple subject eDiary each day throughout the
duration of the study. A final visit will take place at the end of the 8 week treatment
period.
Subjects will receive phone calls at least once a week and subject compliance will be
monitored during the 8 weeks of the study.
pilot study, to evaluate the efficacy and safety of the Vibrant Capsule in relieving
constipation in subjects with functional constipation.
Three arms will be assessed:
- Vibrant Capsule with vibrating mode 1 administered 5 times per week
- Vibrant Capsule with vibrating mode 2 administered 5 times per week
- Sham Capsule administered 5 times per week
Subjects will be followed continuously for at least a 2 weeks run-in period and then be
randomized to either Vibrant or Sham capsules for a treatment period of 8 weeks. The first 2
weeks of treatment will be considered as a subjects' training period.
Data reporting will be done on an electronic Case Report Form and an eDiary. Subjects will be
asked to refrain from taking any medication or supplement to relieve their constipation,
during the entire study period.
After the run-in period, the subjects will return and eligibility will be re-assessed.
Subjects will be trained on how to use the base unit and will swallow the first capsule on
site the day of baseline visit. They will activate and ingest the rest of the capsules at
home by themselves, using the base unit.
Subjects will be instructed to complete a simple subject eDiary each day throughout the
duration of the study. A final visit will take place at the end of the 8 week treatment
period.
Subjects will receive phone calls at least once a week and subject compliance will be
monitored during the 8 weeks of the study.
Inclusion Criteria:
- Subjects aged 22 years and older
- Subjects with Chronic Idiopathic Constipation according to Rome III criteria and who
have not experienced relief of their symptoms from available therapies
- Subjects with an average of <3 Spontaneous Bowel Movements per week and ≥1 Spontaneous
Bowel Movements per week
- Normal colonoscopy performed within 10 years prior to study participation, unless the
subjects are <50 years old and without alarm signs and/or symptoms
- Subject signed the Informed Consent Form
- Female subjects must have a negative pregnancy test
Exclusion Criteria:
- History of complicated/obstructive diverticular disease
- History of intestinal or colonic obstruction, or suspected intestinal obstruction.
- History of significant gastrointestinal disorder, including any form of inflammatory
bowel disease or gastrointestinal malignancy
- History of gastroparesis
- Use of any of the following medications:
- Medications that may affect intestinal motility, prokinetics, anti-Parkinsonian
medications, opiates, opioids, calcium-channel blockers, aluminum/magnesium hydroxide
- With the exception of antidepressants, thyroid or hormonal replacement therapy, when
the subject has been on a stable dose for at least 3 months prior to enrollment.
- Clinical evidence of significant respiratory, cardiovascular, renal, hepatic, biliary,
endocrine, psychiatric or neurologic disease.
- Presence of cardiac pacemaker or gastric electrical stimulator.
- History of, or current eating disorders, such as anorexia, bulimia, or compulsory
overeating.
- Diagnosis of mega-rectum or colon, congenital anorectal malformation, clinically
significant rectocele, history of intestinal resection (with an exception for
appendectomy, cholecystectomy and inguinal hernia repair), history of bariatric
surgery or evidence of any structural abnormality of the gastrointestinal tract that
might affect transit
- History of Zenker's diverticulum, dysphagia, Barrett's esophagus, esophageal stricture
or achalasia
- Chronic use of non-steroidal anti-inflammatory drugs (NSAIDs)
- Subjects with pelvic floor dysfunction/defecatory disorder
- Participation in another clinical study within one month prior to screening.
- Women who are pregnant or lactating
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