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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03693079
Other study ID # KBU-BAP-17/1-KA-071
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 3, 2017
Est. completion date October 1, 2018

Study information

Verified date July 2018
Source Karabuk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This interventional study investigates the efficacy of Wet cupping therapy on heavy metal levels.The levels of the selected heavy metals will be measured in the blood samples obtained from the participants before and after the interventions


Description:

Wet cupping therapy (WCT) is a traditional therapy which was used for centuries especially for detoxifiying purposes.Current literature also points out its blood clarifiying capacity in order to illuminate the underlying mechanism of this ancient treatment.

Steel industry workers, different from the general population are exposed to heavy metals more often.Conducting a study in this special group where we will evaluate the levels of selected heavy metals in blood before and after the three sessions of WCT might let us know its detoxifiying capacity based on measurable parameters.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date October 1, 2018
Est. primary completion date August 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- Healthy individuals

- Iron and Steel industry workers

Exclusion Criteria:

- having any chronic disorder

- being on daily medication

- wet cupping application in the last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Wet cupping therapy
CT was applied using plastic disposable vacuum cups on the back in the 5 areas of C7 cervical spine (DU14 acupoint), T2-4 lateral spine bilaterally (BL41-42 acupoint) and T6-8 lateral spine bilaterally (BL44-46). The cupping technique procedure was conducted in five phases: Primary suction; cups are left attached to the skin for 5 minutes. Area disinfection; areas are wiped with sterile gauze after disinfection with povidone iodine. Scarification; Superficial incisions (20-30 gauge), 5 mm length and 1-2 mm depth, are made on the skin with a sterile, number 11 surgical blade. Bloodletting and secondary suction; the cups which had been previously removed are placed again on the scarified areas Blood leaks from the capillary vessels of the skin and subcutaneous tissue and fills the cups, which are left in place for 15 minutes. Removing and dressing; the cups full of blood are removed. The areas of application are wiped with sterile gauze and then a dressing is applied

Locations

Country Name City State
Turkey Suleyman Ersoy Safranbolu Karabuk

Sponsors (1)

Lead Sponsor Collaborator
Karabuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Levels of the selected heavy metals in venous blood samples before and after the interventions the levels of the calculated heavy metals will be in ppm 3 months
Secondary Levels of the selected heavy metals in cupping blood samples obtained during the first intervention the levels of the calculated heavy metals will be in ppm 1 month
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