CTRI/2025/05/086754Not yet recruitingPhase 2
Comparative evaluation of the effectsof Hijama bila Shart (Dry Cupping) &Hijama bish shart (Wet Cupping) incases of Waja-al-Unuq (Cervical Spondylosis)
Department of Ilaj Bit Tadbeer1 site in 1 country60 target enrollmentStarted: May 26, 2025Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- •VAS (Visual Analogue Scale)[10]
Study Overview
Brief Summary
Objective of the study:
1.)To evaluate the effects of Hijama bila Shart (Dry Cupping), in Waja-al Unuq
(Cervical Spondylosis).
2.)To evaluate the effects of Hijama bish shart (Wet Cupping), in Waja-al Unuq
(Cervical Spondylosis).
3.)To compare the effects of Hijama bila Shart (Dry Cupping) and Hijama bish
shart (Wet Cupping), in Waja-al Unuq (Cervical Spondylosis).
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 20.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Clinically diagnosed patients of Waja’ al-Unuq (cervical spondylosis) 2)Patients who had given informed written consent and accepted to follow the protocol.
- •Patients of both genders.
- •Patients in the age group of 20-60 years.
- •Cervical spondylosis with or without radiculopathy.
Exclusion Criteria
- •Patients below 20 years and above 60 years.
- •Pregnant and lactating women.
- •Patients of diabetes and hypertension.
- •Patients with severe systemic illnesses.
- •Patients unable to give informed written consent.
- •Patient with nervous disorders like epilepsy & dizziness.
- •Patient having concomitant therapy.
- •Patient with thyroid disease.
- •Patient requiring rescue medicine very frequently or once a week.
Outcomes
Primary Outcomes
•VAS (Visual Analogue Scale)[10]
Time Frame: 7th, 14th, 21st, 28th day
•Vernon and Mior Cervical Spine Questionnaire
Time Frame: 7th, 14th, 21st, 28th day
•X- ray cervical spine Antero-posterior and Lateral view
Time Frame: 7th, 14th, 21st, 28th day
Secondary Outcomes
- •Pain(•Tenderness)
Investigators
Study Sites (1)
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