Clinical Trials for Comparison of Two Kinds of Moxibustion | NCT01366456

Studies
Clinical Trials for Comparison of Two Kinds of Moxibustion

NCT01366456

Sponsor

Semyung University

Status

Unknown status

Last Update Posted

Jun 9, 2011Estimated

Enrollment

40Estimated

Phase

Not Applicable

Conditions

Temperature Change

Interventions

Moxibustion

Countries

South Korea

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Apr 2010

Overall Recruitment Status or Expanded Access Status

Unknown status

Last Known Status

Recruiting

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jun 2011

Primary Completion Date

Jun 2012Estimated

Completion Date

Jun 2012Estimated

First Submitted Date

Jun 2, 2011

First Submission Date that Met QC Criteria

Jun 3, 2011

First Posted Date

Jun 6, 2011Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Jun 8, 2011

Last Update Posted Date

Jun 9, 2011Estimated

Name	Class
Kyunghee University	OTHER

Oversight Module

Has Data Monitoring Committee (DMC)

Yes

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

The purpose of this study is to evaluate efficacy of Shingigu and Charcoal moxibustion scientifically and objectively.

Detailed Description

Moxibustion is traditional treatment that regulate circulation of Qi-blood by making the body warm to prevent and treat disease. Recently many kinds of moxibustion and moxibustion apparatus were developed. However evaluating efficacy of moxibustion is insufficient. Thus, there is need for objective evaluating about efficacy of moxibustion.

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

40Estimated

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Shingigu	Active Comparator	Treat with Shingigu	Device: Moxibustion
Charcoal	Active Comparator	Treat with Charcoal	Device: Moxibustion

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Moxibustion	Device	Comparison of different kinds of moxibustion	Charcoal Shingigu

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Temperature Change after moxa treatment		30 minutes after treatment

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

18~65 years old

Exclusion Criteria:

Hyperthyroidism
Heart disease(Heart failure, angina pectoris, myocardial infarction)
Uncontrolled hypertension (SBP>145mmHg or DBP>95mmHg)
Severe renal disorder
Severe liver disorder
Diabetes Mellitus
Female are in the duration of pregnancy

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

65 Years

Standard Ages

AdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Hoyeon Go, O.M.D.	Semyung University Chungju Hospital	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Semyung University Chungju Hospital	Recruiting	Chungju	North Chungcheong	380-960	South Korea

Intervention Browse Module

MeSH Terms

ID	Term
D009071	Moxibustion

Ancestor Terms

ID	Term
D015670	Acupuncture Therapy
D000529	Complementary Therapies
D013812	Therapeutics

Browse Leaves

Not provided

Browse Branches

Not provided