Cupping in Fibromyalgia

NCT ID: NCT01635634

Last Updated: 2018-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

141 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-06-30

Study Completion Date

2015-03-31

Brief Summary

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The purpose of this randomized controlled study is to determine the effectiveness of cupping in patients with fibromyalgia compared to sham cupping.

Detailed Description

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see above

Conditions

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Fibromyalgia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Sham Cupping

Dry Cupping Therapy 5 serial treatments twice weekly 4-8 cups at the upper and lower back

Group Type SHAM_COMPARATOR

Cupping therapy

Intervention Type OTHER

Cups are placed at the skin; local suction is created on the skin; it mobilizes blood flow; the suction is created by a mechanical device (Pneumatron, Pneumed, Germany)

Cupping Therapy

Dry Cupping 5 serial treatments twice weekly 4-8 cups at the upper and lower back

Group Type EXPERIMENTAL

Cupping therapy

Intervention Type OTHER

Cups are placed at the skin; local suction is created on the skin; it mobilizes blood flow; the suction is created by a mechanical device (Pneumatron, Pneumed, Germany)

Wait list

Wait list control no specific intervention for 3 weeks study period

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Cupping therapy

Cups are placed at the skin; local suction is created on the skin; it mobilizes blood flow; the suction is created by a mechanical device (Pneumatron, Pneumed, Germany)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* FMS diagnosis according to AWMF Guidelines,
* necessary documents: medical records
* Pain intensity \> 45mm VAS
* Participation in cupping twice weekly on appointment

Exclusion Criteria

* pregnancy
* other study participation
* pain due to other rheumatic disease
* major psychiatric disorder
* substance abuse
* severe somatic disorder (cancer)
* injections, acupuncture, neural therapy within the past 3 months
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universität Duisburg-Essen

OTHER

Sponsor Role lead

Responsible Party

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Jost Langhorst

Prof. Dr. med.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jost Langhorst, MD, Prof

Role: PRINCIPAL_INVESTIGATOR

University of Duisburg-Essen

Locations

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Klinik für Naturheilkunde

Essen, , Germany

Site Status

Countries

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Germany

References

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Lauche R, Spitzer J, Schwahn B, Ostermann T, Bernardy K, Cramer H, Dobos G, Langhorst J. Efficacy of cupping therapy in patients with the fibromyalgia syndrome-a randomised placebo controlled trial. Sci Rep. 2016 Nov 17;6:37316. doi: 10.1038/srep37316.

Reference Type BACKGROUND
PMID: 27853272 (View on PubMed)

Related Links

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Other Identifiers

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CuFib

Identifier Type: -

Identifier Source: org_study_id

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