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Taking people in PakistanPhase 3

Tests herbal medicine Qurs e Fishar for mild to moderate high blood pressure

Tests an herbal medicine, Qurs e Fishar, in adults with mild to moderate hypertension.

Plain-language title generated from the registry record
Registry title: Safety & Efficacy of Qurs e Fishar in Mild to Moderate Hypertensive Patients in Pakistan

Key facts

Where
Karachi, PakistanSee the site
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 30 and 60 years old?

Source: NCT06852079, who can take part

Where in Pakistan

  • Taj Medical Complex, Hamdard University HospitalKarachi, PakistanTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Abdul Bari
Trial code
NCT06852079
Record updated
28 February 2025
Original description
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.Read full original descriptionShow less

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

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.

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

ClinicalTrials.gov NCT06852079