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Assessing the Efficacy of Hammam and Dawaul Misk Motadil Sada in Managing Primary Hypertension

To Evaluate the Therapeutic effects of Hammam and Dawaul Misk Motadil Sada in management of Zaght Al-Dam Qawi Ibtidai (Primary Hypertension). A Randomized open labelled Standard Control Study. - NIL

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054266
Enrollment
159
Registered
2023-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I10- Essential (primary) hypertension

Interventions

Intervention1: Dawaul Misk Motadil Sada for 12 weeks: Dawaul Misk Motadil Sada is a semi-solid compound Unani pharmacopoeial formulation taken from NFUM part III. The semi solid drug has been used by

Sponsors

Research Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of hypertension with SBP 140-179 mm of Hg and DBP 90-100 mm of Hg 2. Ambulatory Blood Pressure Monitoring for at least one day. 3. Willingness to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patient with SBP >=180 mm of hg and diastolic BP >100 mm of hg and secondary hypertension, 2. Pregnant and lactating females, 3. Females using oral contraceptive pills regularly, 4. Patients taking any other medication affecting blood pressure like NSAIDs, 5. Patients with abnormality in investigations done at baseline (SGPT >105 IU). 6. Obese subjects â?? BMI >30, patients with disorders requiring long term-treatment, e.g., diabetes mellitus, drug addicts, alcoholics /malignancy /epilepsy /CAD/CKD, patients with sinus bradycardia, i.e., pulse rate less than 60/min. 7. Treatment defaulters 8. Life threatening medical problems

Design outcomes

Primary

MeasureTime frame
Reduction in systolic and diastolic blood pressure levels. To achieve a target blood pressure level that is associated with a lower risk of cardiovascular events.Timepoint: The patients will be assessed clinically at every 2 weeks i.e., at 14, 28, 42, 56, 70 and 84, The subjective and objective clinical observations will be recorded in the follow-up sheet.

Secondary

MeasureTime frame
Adverse events:Such as dizziness, fatigue, or gastrointestinal symptoms. These adverse events should be monitored and reported as secondary outcomes. SUBJECTIVE PARAMETERS: Suda (Headache), Duwar (Vertigo), Khafqan (Palpitation), Kasal (Laziness), Qalaq (Anxiety), Usr al-tanaffus (Breathlessness), Takaddurfiâ??lhawas (Diminished alertness), Ruâ??af (Epistaxis) and Nabz mumtali (Pulsus plenus) should be assessed. Quality of life: Hypertension can impact a persons quality of life, and reducing blood pressure can improve quality of life measures such as physical functioning, mental health, and social functioning. Cost-effectiveness: The cost-effectiveness of hypertension treatments is an important consideration for healthcare decision-making. A study can include a secondary outcome measure that evaluates the cost-effectiveness of a hypertension treatment.Timepoint: 12 weeks

Countries

India

Contacts

Public ContactDr Aamir Yousuf

Regional Research Institute of Unani Medicine (RRIUM), Srinagar

draamir.rrium@gmail.com9596079069

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026