About this trial

The proposed research is to determine the clinical efficacy and neurobiological mechanisms of acupuncture analgesia in patients with sickle cell disease.

Eligibility criteria

Qualifiers

Any gender

14-17 (Adolescents) and 18-80 (Adults) years old

Right-handed

Either outpatient or inpatient or status changing between each other

Disqualifiers

Subjects with Covid-19 suspicion or confirmation

Recent/ongoing alternative pain management with acupuncture or acupuncture-related techniques within the last 6-months.

Presence of a known coagulation abnormality: Thrombocytopenia (mild thrombocytopenia with a platelets range of 51,000-100,000/ul will be further evaluated for inclusion consideration), or bleeding diathesis that may preclude the safe use of acupuncture.

Presence of a concurrent autoimmune or inflammatory disease such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, etc. that causes pain or any other chronic pain condition with pain greater than sickle pain.

Trial design

Treatments tested in this trial

  • needling acupuncture
  • laser acupuncture

Treatment groups

120 Participants
are divided into 4 treatment groups

Locations

1
Indiana University School of Medicine46075, IndianapolisIndiana, United States

Sponsors and collaborators

Indiana University

Lead sponsor