Hypertension Clinical Trial
Official title:
The Efficacy of Wet Cupping on Blood Pressure Among Hypertension Patients in Jeddah, 2013, A Pilot Study
| NCT number | NCT01853371 |
| Other study ID # | 001 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | May 7, 2013 |
| Last updated | November 24, 2014 |
| Start date | June 2013 |
| Verified date | November 2014 |
| Source | King Abdulaziz University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Saudi Arabia: Ministry for Higher Education |
| Study type | Interventional |
This research proposal is submitted to fulfill the requirement of the PHD degree of
Community Medicine Saudi Board at the Joint Program of Family and Community Medicine in
Jeddah, Saudi Arabia.
Background: Cupping is an ancient treatment remedy that has been used for many centuries in
many parts of the world. In the Middle East, Wet cupping "Hijama" is still a popular
treatment because of its religious background. Despite of that, it still has little
scientific evidence that proves its efficacy. Many hijama healers claim that they have
observed dramatic improvement in Blood pressure control of hypertension patients. Not many
studies support that. This study should help to prove or disprove this hypothesis.
Objectives:
- To determine the efficacy of wet cupping on blood pressure among high blood pressure
patients.
- To assess the incidence of wet cupping side effects in the intervention group.
Methods: The study design is a randomised controlled trial. There will be an intervention
group of high blood pressure patients who will perform hijama in addition to their usual
management, and a control group of high blood pressure patients who will receive their usual
anti-hypertension management only. There will be 4 weeks follow up period. After that, data
entry, analysis and interpretation will take place.
Hypothesis: Wet cupping has an effect on blood pressure in adult hypertension patients
| Status | Completed |
| Enrollment | 20 |
| Est. completion date | |
| Est. primary completion date | November 2013 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 19 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - High BP at the time of the study (SBP 140 mmHg or more and/or DBP 90mmHg or more). For patients with DM, high BP is defined as SBP 130 mmHg or more and/or DBP 85mmHg or more. - Age between 19 and 65 years old. - Males and females Exclusion Criteria: - Grade III Hypertension (SBP 180 mmHg or more and/or DBP 110 BP or more). - Patients with very high added risk,according to the Saudi Hypertension management guidelines. By excluding the patient who have associated clinical conditions which are: cerebrovascular disease, heart disease, renal disease, peripheral vascular disease and advanced retinopathy. - Patients with secondary hypertension. - Pregnant women. - If the patient performed dry cupping, wet cupping or acupuncture during the past 6 months. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Saudi Arabia | King Abdulaziz University Hospital | Jeddah | Western region |
| Lead Sponsor | Collaborator |
|---|---|
| King Abdulaziz University | Joint Program of Family and Community Medicine, Jeddah, Saudi Arabia, King Fahd Medical Research Centre |
Saudi Arabia,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Systolic Blood Pressure After 4 Weeks | 1 month | No | |
| Primary | Diastolic Blood Pressure After 4 Weeks | 1 month | No | |
| Secondary | Incidence of Wet Cupping Side Effects in Intervention Group | Immediate side effects of wet cupping will be assessed through a checklist on the after each cupping session. Delayed side effects of wet cupping will be assessed through another checklist after 1 month of the final hijama session. |
1 month | Yes |
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