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Effectiveness of Pharmacopuncture for Chronic Neck Pain

A Study on the Effectiveness of Pharmacopuncture for Chronic Neck Pain: A Protocol for a Pragmatic Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04035018
Enrollment
101
Registered
2019-07-29
Start date
2019-09-18
Completion date
2020-06-25
Last updated
2020-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Neck Pain

Brief summary

In this study, the investigators will evaluate the efficacy and safety of pharmacopuncture therapy for chronic neck pain compared to physical therapy.

Detailed description

This study is prgmatic RCT of pharmacopuncture therapy for chronic neck pain compared to physical therapy.

Interventions

The participants in the treatment group will be receive one or more pharmacopuncture therapy according to the physician's decision.

PROCEDUREPhysical therapy

The participants in the control group will be receive one or more physical therapy according to the physician's decision.

Sponsors

Jaseng Medical Foundation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Neck pain more than 6 months * VAS of neck pain more than 5 * Age between 17 and 70 years old * Participants who wrote informed consent

Exclusion criteria

* Migration of cancer reaching to spine, fracture of spine * Progressive neurologic deficits or severe neurologic deficits * Cancer, fibromyalgia, RA, or goat * Stroke, MI, kidney disease, dimentia, diabetic neuropathy, or epilepsy * Participants taking steroid, immunosuppressant, or psychotropic medication * Hemorrhagic disease, severe diabetes or taking anticoagulant drug * Participants who took NSAIDs or pharmacopuncture within 1 week * Pregnant or lactating women * Participants who had undergone cervical surgery within 3 months * Participants who had participated in other clinical trial within 1 month, or have plan for participation in other trial during follow up period of this trial * Participants who can not write informed consent * Participants who is difficult to participate in the trial according to investigator's decision

Design outcomes

Primary

MeasureTime frameDescription
Visual analogue scale of neck painweek 6Minimum 0, Maximum 100. Higher values represent a worse outcome

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026