Pain Clinical Trial
Official title:
The Effect of Acupuncture on Pain, IL 17 and IL 23 in Endovenous Ablation; Prospective, Randomized, Controlled Study.
Verified date | March 2019 |
Source | Kahramanmaras Sutcu Imam University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Acupuncture has emerged in China about 2,000 years ago and is one of the oldest medical procedures in the world. Acupuncture continued to evolve and develop over the centuries, and gradually became one of the standard treatments used in China. Introduced to other regions such as Asia, Europe and the United States. The most extensive use of acupuncture is for pain relief. The aim of this study was to prevent complications due to pain frequently seen in patients who would be treated with endovenous ablation in the postoperative period. In addition, the effect of acupuncture on operative hemodynamics, pain, vascular diameter, postoperative, nausea, vomiting, pain and analgesic needs, IL17 and IL 23.
Status | Completed |
Enrollment | 70 |
Est. completion date | March 7, 2019 |
Est. primary completion date | March 5, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Volunteers to participate in the study, - 18-65 years of age, - patients with a saphenous vein diameter greater than 5.5 mm - small saphenous vein diameter of less than 4 mm with reflux for greater than 0.5 s Exclusion Criteria: - Patients outside the 18-65 age range, - patients with deep venous system obstruction, - patients who have previously used another invasive treatment method (thermal and chemical ablation, surgery), - patients with heart and kidney failure, - patients with secondary varicose veins, - patients with hypercoagulable state patients, - patients with local or systemic infections, - patients with obesity (body mass index> 35), - patients with impaired consciousness, - patients who do not want to participate in the study. |
Country | Name | City | State |
---|---|---|---|
Turkey | Kahramanmaras Sutcu Imam University Faculty of Medicine | Kahramanmaras | Onikisubat |
Lead Sponsor | Collaborator |
---|---|
Kahramanmaras Sutcu Imam University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | IL 17 and IL 23 values | Change From Baseline on the circulating levels of IL 17 and IL 23 ng/ L | before operation and after the operation 3. days | |
Primary | Pain (VAS Score) | Change from Baseline VAS Score. from 1 to 10 , 0: No pain, 10: 10 pain that can not be tolerated | Change From Baseline of VAS Score in 1 minute,3 minute,5 minute,7 minute, 10 minute, 15 minute of pain level during operation.Each unit will be evaluated separately within itself | |
Primary | Pain (VAS Score) | Change from Baseline VAS Score (Visual analog scale) Score. from 1 to 10 , 0: No pain, 10: 10 pain that can not be tolerated | Change From Baseline of VAS Score in1 minute,30 minute, 60 minute after operation and 3. days. Each unit will be evaluated separately within itself | |
Secondary | vessel measurement | Change from Baseline measurement (mm)with ultrasonografi | before the operation, after operation and after operation 3. days |
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