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Trials / Completed

CompletedNCT02090686

Pulsatile Cupping in Low Back Pain

Efficacy of Pulsatile Cupping in Patients With Chronic Low Back Pain - a Randomized Controlled Study.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Charite University, Berlin, Germany · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether pulsatile cupping with a cupping device is effective in the treatment of patients with chronic low back pain compared to no cupping or to minimal cupping.

Conditions

Interventions

TypeNameDescription
DEVICEPulsatile Cupping8 cupping sessions (each 8 minutes) in 4 weeks (-150 to -350 mbar), interval 2 seconds. Paracetamol on demand as rescue medication (maximum dosage 4 x500 mg/day)
DEVICEMinimal Cupping8 cupping sessions (each 8 minutes) in 4 weeks witth (-60 to -70 mbar). Paracetamol on demand as rescue medication (maximum dosage 4 x500 mg/day).

Timeline

Start date
2014-03-01
Primary completion
2014-10-01
Completion
2015-02-28
First posted
2014-03-18
Last updated
2018-02-20

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02090686. Inclusion in this directory is not an endorsement.

Pulsatile Cupping in Low Back Pain (NCT02090686) · Clinical Trials Directory