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

NCT ID: NCT06271525

Last Updated: 2024-02-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-20

Study Completion Date

2024-05-20

Brief Summary

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

Detailed Description

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Cupping therapy is one of the oldest alternative medical procedures, along with acupuncture, with more than 3500 years of history to treat pain and various disorders. Cupping induces various biological responses that could be evoked by suction of the skin, About 5 to 10 minutes of cupping causes extravascular blood within the subcutaneous tissue and creates bruise-like marks. Therefore, cupping induces mild damage to a painful part of the body and accelerates healing by evoking the natural healing process. While this hypothesis is acceptable for some people, it might not be enough to change the minds of skeptics since cupping itself has no curative effects. Suppose the healing process after cupping can be accelerated by merging cupping with scientifically proven techniques. In that case, this new form of therapy might help to persuade skeptics of the efficacy of cupping. Integrative medicine, including acupuncture, dry needling, and cupping, is being used increasingly in the United States. evidence regarding their efficacy in the management of musculoskeletal conditions is heterogeneous and subject to several limitations. despite these limitations, acupuncture consistently is more effective than no treatment and is relatively safe. for chronic back pain, it is recommended as a first-line noninvasive therapy. for neck pain, acupuncture provides benefits when it is combined with other treatments. dry needling is similar to acupuncture and frequently is regarded as a form of acupuncture. sixty patients with cervical spondylosis will receive cupping therapy for three months.

Conditions

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Cervical Spondylosis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

cupping therapy
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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cupping therapy

patients with cervical spondylosis will receive cupping therapy one time per month for three months

Group Type EXPERIMENTAL

cupping therapy

Intervention Type OTHER

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

Interventions

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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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with (cervical spondylosis) from both sexes.
* Age range (24-60) in chronic stages.
* BMI from20-25 kg/m2.

Exclusion Criteria

* Renal and hepatic patients.
* Anemia, hepatic disease, and dermatological diseases.
* Morbid obese patients if their BMI exceeds the 25 kg/m2 will be also excluded.
* the patients are taking any medications known to affect the pain level
* The patients have a systemic illness, dermatological problems, skin allergy, local ischemic problems
Minimum Eligible Age

24 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shady Abdelsattar Refaat

OTHER

Sponsor Role lead

Responsible Party

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Shady Abdelsattar Refaat

principle investigator shady abdelsattar refaat

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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P.T.REC/012/002532

Identifier Type: -

Identifier Source: org_study_id

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