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
| Type | Name | Description |
|---|---|---|
| DEVICE | Pulsatile Cupping | 8 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) |
| DEVICE | Minimal Cupping | 8 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.