NCT01452386

Brief Summary

To prove the modify functional magnetic stimulation could improve constipation.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Jun 2011

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2011

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 11, 2011

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 14, 2011

Completed
4.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2016

Completed
Last Updated

November 8, 2016

Status Verified

November 1, 2016

Enrollment Period

5 years

First QC Date

October 11, 2011

Last Update Submit

November 6, 2016

Conditions

Constipation

Keywords

ConstipationStimulation Treatment

Outcome Measures

Primary Outcomes (1)

  • To improve bowel movement by the modify functional magnetic stimulation

Study Arms (2)

Experimental Group

Control Group

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

constipation patients

You may qualify if:

  • Patients who age between 20\~60 years old and have suffered from chronic constipation for more than 6 months will be enrolled in this study.

You may not qualify if:

  • Patients with implantation chip of brain
  • Patients with implantation of pacemaker
  • Patients with heart transplantation
  • Patients are embedded electronic and Life support products.
  • People who have be implanted metal、electronic devices、artificial joints or fixator.
  • Patients with hemiplegia
  • Patients with peripheral neuritis
  • Patients with Prostate abnormalities
  • Patients with Pregnancy
  • Patients with Fever
  • Patients with Injure
  • Patients with Heart disease
  • Patients with Consciousness disturbance
  • Patients with Organic constipation
  • Patients with Kidney stone
  • +1 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taipei Medical University - WanFang Hospital

Taipei, Taiwan

Location

MeSH Terms

Conditions

Constipation

Condition Hierarchy (Ancestors)

Signs and Symptoms, DigestiveSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Fat-Moon Suk

    Taipei Medical University WanFang Hospital

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 11, 2011

First Posted

October 14, 2011

Study Start

June 1, 2011

Primary Completion

June 1, 2016

Study Completion

June 1, 2016

Last Updated

November 8, 2016

Record last verified: 2016-11

Locations

TW(1)