Skip to content

Stresswin in Hypertension

Validation & Dissemination of Polyherbal formulation for Management of Hypertension

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052806
Enrollment
30
Registered
2023-05-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

None listed

Sponsors

IOE, BHU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing to participate in the study. 2. Patients of either sex with ages between 18-60 years. 3. Patients having Hypertension between the time intervals of 6 months to 1 year. 4. Patients suffering from Stage I Hypertension (Systolic Blood Pressure 140-159mm of Hg, Diastolic Blood Pressure 90-99mm of Hg) 5. Patients suffering from Stage I Hypertension are those who are on allopathic medicines. 6. Patients suffering from Isolated Systolic Hypertension.

Exclusion criteria

Exclusion criteria: 1. Patients not willing to participate in the study. 2. Patients of either sex below 18 years & above 60 years will be excluded from the study. 3. Patients having Hypertension for 1 year will be excluded. 4. Patients of Stage II Hypertension (Systolic Blood Pressure >160mmHg and Diastolic Blood Pressure >100mmHg) 5. Patients suffering from serious comorbidities like renal failure, coronary artery disease, Type 2 Diabetes Mellitus, cervical spondylosis, taking medications/drugs (oral contraceptives, steroids, chronic use of NSAIDs etc.). 6. Alcoholics and/or drug abusers. 7. History of hypersensitivity to the trial drug or any of its ingredients. 8. Pregnant/ lactating woman. 9. Patients who have completed participation in any other clinical trial during the past 6 months.

Design outcomes

Primary

MeasureTime frame
Normalization of Blood Pressure within one month of interventionTimepoint: 4 weeks

Secondary

MeasureTime frame
Reduce Stress Sound sleep Reduce Palpitations Timepoint: 1 week

Countries

India

Contacts

Public ContactSanjeev Kumar

Institute of Medical Sciences, BHU

kumarsanjeevdg@bhu.ac.in

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026