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Effects of Bloodletting Acupuncture for Subacute and Chronic Non-specific Low Back Pain

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Enrolling

Conditions

Back Pain, Low

Treatments

Procedure: Bloodletting acupuncture at the fossa poplitea
Procedure: Bloodletting acupuncture at the regio glutaea

Study type

Interventional

Funder types

Other

Identifiers

NCT06190366
Mikroaderlass

Details and patient eligibility

About

Evaluation of a bloodletting acupuncture at the fossa poplitea in comparison to bloodletting acupuncture at the regio glutaea and a waiting list control group in patients with subacute and chronic non-specific pain low back pain.

Enrollment

108 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Specialist confirmed diagnosis of subacute or chronic non-specific low back pain for at least 6 weeks prior to inclusion
  • Average pain intensity with at least 50 mm on the VAS from 0 to 100 mm

Exclusion criteria

  • Serious illnesses
  • Poor general condition
  • Coagulation disorder, therapy with anticoagulants
  • Thrombophlebitis, skin inflammation in the area of the lower extremities
  • Alcohol, drug or medication addiction
  • Pregnancy
  • Lack of willingness to cooperate, linguistically or mentally unable to understand the contents of the study
  • Participation in another clinical trial during the study period
  • Starting a new therapy for the treatment of low back pain in the last 2 weeks

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

108 participants in 3 patient groups

Bloodletting acupuncture at the fossa poplitea
Experimental group
Treatment:
Procedure: Bloodletting acupuncture at the fossa poplitea
Bloodletting acupuncture at the regio glutaea
Experimental group
Treatment:
Procedure: Bloodletting acupuncture at the regio glutaea
Waiting list control group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Miriam Rösner

Data sourced from clinicaltrials.gov

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