Using battlefield acupuncture to relieve pain in hidradenitis suppurativa
Official title: Battlefield Acupuncture to Treat Pain in Hidradenitis Suppurativa
Run by Wayne State University · NCT04218422 · Data updated 2026-11-12
This study is testing if battlefield acupuncture can help reduce pain for people with hidradenitis suppurativa.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 32 (estimated) |
| Sponsor | Wayne State University Academic / other |
| Locations | 1 site (Dearborn, Michigan) |
| Status | Recruiting |
| Started | January 22, 2020 |
| Main results expected | December 23, 2030 |
| Study ends | February 20, 2031 |
| Registry record updated | May 16, 2023 |
| Trial ID | NCT04218422 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older with a dermatologist-confirmed diagnosis of hidradenitis suppurativa and significant pain occurring at least twice weekly.
✕Probably not a fit
Patients with ear conditions that prevent acupuncture or those with other chronic pain issues that interfere with pain assessment may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the effectiveness of battlefield acupuncture as a treatment for pain associated with hidradenitis suppurativa. Participants will report their pain levels daily over a four-week period, receiving acupuncture in the ears during the second and third weeks. The study aims to determine if this acupuncture technique can significantly reduce pain for individuals suffering from this condition.
Why it matters
Potential benefit: If successful, this approach could provide a non-pharmacological option for managing pain in patients with hidradenitis suppurativa.
How similar studies have gone: While acupuncture has been explored in various pain management contexts, the specific application of battlefield acupuncture for hidradenitis suppurativa is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * age 18 years or older * dermatologist-confirmed diagnosis of hidradenitis suppurativa * significant pain from hidradenitis at least twice weekly * stable treatment regimen for hidradenitis during study period Exclusion Criteria: * disease or disfigurement of the ear that prevents battlefield acupuncture of the ears * other chronic pain that will interfere with the ability to rate hidradenitis pain
Where it's running
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WSUPG Dermatology
Dearborn, Michigan, United States Recruiting
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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BTK inhibitor remibrutinib in hidradenitis suppurativa shows how it works in adults
This phase 1 trial tests whether remibrutinib can safely affect HS in adults with moderate to severe disease.
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Olatorepatide vs placebo for adults with moderate-to-severe hidradenitis suppurativa who are overweight
This study tests whether olatorepatide can help people with hidradenitis suppurativa who are overweight or obese.
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Remibrutinib extension study for adults with moderate to severe hidradenitis suppurativa
This extension study tests whether continuing remibrutinib is safe and helps skin symptoms in adults who completed prior HS trials.
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LAD328 in adults with hidradenitis suppurativa
This study tests whether LAD328 works better than placebo for adults with moderate-to-severe hidradenitis suppurativa.
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Long-term real-world tracking of secukinumab treatment for moderate to severe hidradenitis suppurativa in Italy
This project will see how secukinumab works and is used in adults with moderate to severe hidradenitis suppurativa in Italy.
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Secukinumab outcomes in Canadians with hidradenitis suppurativa
It will see how well secukinumab works and how safe it is for adults in Canada with moderate-to-severe hidradenitis suppurativa who were newly prescribed it in routine care.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.