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Effect of Cupping Therapy on Microcirculation in Healthy Volunteers (CTWN)

T

Tokat Gaziosmanpasa University

Status

Completed

Conditions

Microcirculation

Treatments

Diagnostic Test: Vascular occlusion test
Procedure: cupping therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06872216
NIRS-CUPPİNG

Details and patient eligibility

About

Twenty healthy volunteers were included in the study. The NIRS was placed on the thenar region of the hand. The vascular occlusion protocol had been done before and after cupping therapy (CT). Regional oxygen saturation (rSO2), the times to the lowest and highest values were recorded. The occlusion slope, the recovery slope and the first 10 second recovery slope were calculated.

Full description

Participants rested in a seated position at standard temperature for at least 10 minutes. A blood pressure cuff was applied to the upper arm, and the NIRS device (Covidien INVOS™ 5100C Cerebral/Somatic Oximeter, Dublin) was used to monitor regional oxygen levels in the thenar region of the hand throughout the protocol. After a 3-minute stabilization period, the vascular occlusion protocol commenced: the blood pressure cuff was inflated rapidly within 3-4 seconds to 50 mmHg above the baseline systolic blood pressure and maintained for 3 minutes, then deflated within 1 second. The participant rested for another 10 minutes before a certified cupping therapist placed a plastic therapy cup on the forearm, 5 cm from the medial and lateral epicondyles. The size of the cup was based on the participant's forearm, covering 50% of the area. The cup was vacuumed twice using a manual hand pump and left in place for 5 minutes before the air was released through the valve. Following a 3-minute stabilization period, the vascular occlusion protocol was repeated. During the test, rSO2 values and the time to reach the lowest and highest values were recorded. Using this data, the occlusion slope, recovery slope, and 10-second recovery slope were calculated. The occlusion slope was determined by the formula [(baseline rSO2 - minimum rSO2) / time to lowest rSO2], in %/minute. The recovery slope was calculated as [(minimum rSO2 - maximum rSO2) / time to reach the highest rSO2], in %/second. The 10-second recovery slope was calculated as [(minimum rSO2 - rSO2 at 10 seconds) / 10 seconds].

Enrollment

20 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-65 years old
  • Healthy

Exclusion criteria

  • Smoking or using tobacco products
  • Taking alcohol or other substances, or any medication
  • Have conditions affecting microcirculation
  • Have acute or chronic pain
  • Anemia
  • Obesity
  • Reynaud's phenomenon
  • Baseline blood pressure being 140-90mmHg or above
  • sPO2 value being below 96%

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

cupping therapy
Other group
Description:
nırs monitored during vot test pre-post cupping therapy
Treatment:
Procedure: cupping therapy
Diagnostic Test: Vascular occlusion test

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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