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Performance, Efficacy and Safety of Vibrating Capsule in Aiding Constipated Individuals

NCT02030756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 144

Last updated 2017-11-07

No results posted yet for this study

Summary

This is a study intended to evaluate the efficacy and safety of the vibrating capsule versus sham non-vibrating capsule on spontaneous bowel movement, in aiding reliving Constipated Individuals

Conditions

  • Chronic Idiopathic Constipation

Interventions

DEVICE

vibrating capsule

patients will receive vibrating capsule for 8 weeks of treatment \[1 every 3 days (+/- 1 day)\].

DEVICE

sham non-vibrating capsule

patients will receive sham non-vibrating capsule for 8 weeks of treatment \[1 every 3 days (+/- 1 day)\].

Sponsors & Collaborators

  • Vibrant Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2016-01-31
Completion
2016-02-29

Countries

  • United States
  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02030756 on ClinicalTrials.gov