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Effect of Cupping Therapy on Nitric Oxide Level in Patients With Cervical Spondylosis

NCT06271525 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-02-21

No results posted yet for this study

Summary

this study will be conducted to investigate the effect of cupping therapy on the nitric oxide level in patients with cervical spondylosis

Conditions

  • Cervical Spondylosis

Interventions

OTHER

cupping therapy

All the patients will be asked to be in a sitting position with both feet flat on the floor the cupping group will receive the cupping bloodletting at three acupuncture points (SI15, GB21, LI15) the medium size glass with a diameter of 4cm and a volume of 260ml. Each wet cupping treatment procedure will last about 20 min and will be conducted in five steps. 1. -Primary sucking 2. -Scarification 3- Bloodletting 4-Removal 5 -Dressing

Sponsors & Collaborators

  • Shady Abdelsattar Refaat

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
24 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-20
Primary Completion
2024-05-20
Completion
2024-05-20

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06271525 on ClinicalTrials.gov