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NCT04035018 Clinical Trial

Effectiveness of Pharmacopuncture for Chronic Neck Pain

Chronic Neck Pain Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04035018
Other study ID # JS-CT-2019-04
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 18, 2019
Est. completion date June 25, 2020

Study information
Verified date July 2020
Source Jaseng Medical Foundation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 101
Est. completion date June 25, 2020
Est. primary completion date June 25, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 70 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• pharmacopuncture therapy
The participants in the treatment group will be receive one or more pharmacopuncture therapy according to the physician's decision.
• Physical therapy
The participants in the control group will be receive one or more physical therapy according to the physician's decision.

Locations
Country Name City State
Korea, Republic of Bucheon Jaseng Hospital of Korean Medicine Bucheon Gyeonggi Province
Korea, Republic of Haeundae Jaseng Hospital of Korean Medicine Busan
Korea, Republic of Daejeon Jaseng Hospital of Korean Medicine Daejeon
Korea, Republic of Jaseng Hospital of Korean Medicine Seoul Gangnam-Gu

Sponsors (1)
Lead Sponsor Collaborator
Jaseng Medical Foundation

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual analogue scale of neck pain Minimum 0, Maximum 100. Higher values represent a worse outcome week 6
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