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To evaluate the Safety and efficacy of Unani formulation in the treatment of Palpitatio

Phase 2
Conditions
Health Condition 1: null- Khafaqan (Palpitation)Health Condition 2: R002- Palpitations
Registration Number
CTRI/2015/02/005525
Lead Sponsor
Central Council for Research in Unani MedicineCCRUM
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
300
Inclusion Criteria

•Patients of either sex in the age group of 18-60

•Patients of Palpitation (heart rate: < 60 or >100 bpm) with and without any of the following symptoms/ signs:

ï?§Ghabrahat

ï?§Feeling of Missed Beat

ï?§Discomfort in Chest

ï?§Sweating

ï?§Dizziness

Exclusion Criteria

•History of any heart diseases

•History of hepatic, renal disorders, diabetes mellitus, hypertension, anaemia, COPD

•History of thyroid dysfunction

•History of hypersensitivity to any ingredient of the study drug.

•Participants with history of long term use of any other drugs such as anti-epileptic, anti-arrhythmic and anti-psychotic drugs etc.

•History of Addiction (smoking, alcohol, drugs)

•Pregnant and lactating women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement in signs and symptomsTimepoint: 4 weeks
Secondary Outcome Measures
NameTimeMethod
Hematological and biochemical assessments for safetyTimepoint: 4 weeks
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