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Safety & Efficacy of Qurs e Fishar in Mild to Moderate Hypertensive Patients in Pakistan

Safety & Efficacy of Qurs e Fishar in Mild to Moderate Hypertensive Patients in Pakistan

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06852079
Enrollment
119
Registered
2025-02-28
Start date
2023-12-23
Completion date
2025-12-31
Last updated
2025-02-28

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

Conditions

Hypertension

Keywords

HTN, Hypertension, Qurs e Fishar

Brief summary

The herbal medicine Qurs-e-Fishar to treat mild to moderate High blood pressure or hypertension comprises of Rauwolfia serpentina. A product of Hamdard Laboratories (Waqf) Pakistan. A Phase III Safety & Efficacy Open-label, Single-Arm, Interventional, Multicenter, Study in mild to moderate hypertensive, adults (30 to 60 years of age) prescribed with study product for 12 weeks (84 days). Primary End Points: 1. Reduction in diastolic blood pressure less than 130 / 80 mmHg at the end of the study period (accepted by WHO) or if there was a fall of 20 / 10 mmHg or more in diastolic blood pressure as compared to baseline. 2. Type, frequency and severity of ADRs during the study period. Secondary End Points: 1\. Compliance of the prescribed study medication.

Interventions

OTHERQurs e Fishar

Qurs e Fishar is a herbal remedy for Hypertension

Sponsors

Hamdard University
CollaboratorOTHER
Abdul Bari
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Ability to sign ICD * Participant(s) are willing and able to fulfill the requirements of the study protocol * Mild to moderate hypertensive * Mild hypertension range (140-159/90-99 mm Hg) * Moderate hypertension range (160-179/100-109 mm Hg) * Be between the age of 30 to 60 year

Exclusion criteria

* Patients with recent history of following will be excluded: * Severe hypertension, * Congestive cardiac failure, * Left ventricular failure, * Myocardial ischemia, * Renal failure or * Cerebrovascular accidents

Design outcomes

Primary

MeasureTime frameDescription
Blood Pressure12 weeksBlood pressure (in mmHg) will be measure at baseline and again at first follow-up (4th week), than at second follow-up (at 8th week) the end of treatment (12th week).

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026