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A clinical trial to compare the effect of two drugs Habb-e-Baqla and Sharbat e Ejaz in patients with cough

Comparative Clinical validation study to evaluate the safety and efficacy of Unani Pharmacopeial formulation Habb-e-Baqla vs Sharbat e Ejaz in Sual (Cough) - NILL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092556
Enrollment
210
Registered
2025-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: R05- Cough

Interventions

Intervention1: Habb-e-Baqla: 2 tabs 500mg (each) twice daily orally for 14 days. Control Intervention1: Sharbat e Ejaz: 20 ml twice daily with lukewarm water for 14 days

Sponsors

Central Council for Research in Unani Medicine CCRUM New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Dry cough with onset not more than 3 weeks with/without Khushunat e Halq.

Exclusion criteria

Exclusion criteria: 1. Any specific symptoms that signify any history of serious lower respiratory tract infection, such as pneumonia, lung abscess, bronchiectasis, emphysema, pneumothorax, hydrothorax, COPD, or pulmonary tuberculosis. 2. Cough associated with high-grade fever. 3. Known cases of any other clinically significant comorbid conditions, like severe renal,hepatic and cardiovascular disorders. 4. Known cases of immunocompromised conditions such as HIV/AIDS, cancer, etc. 5. Diabetes mellitus, hypertension or any other systemic disorders requiring prolonged treatment. 6. Pregnant and lactating females.

Design outcomes

Primary

MeasureTime frame
The safety and efficacy of Unani Pharmacopeial formulation Habbe Baqla in comparison with Sharbat e Ejaz in Sual (Cough) will be carried out on the basis of a cough Visual Analogue Scale (VAS), Khushunat e Halq (Visual analogue scale) and Cough Symptom Score (CSS).Timepoint: At 7th and 14th day of treatment.

Secondary

MeasureTime frame
Haematological and biochemical investigations for safety assessment i.e., Hemogram, Urine Examination: Routine & Microscopic.Timepoint: At baseline, first follow up and at the end of treatment. i.e., 0, 7th and 14th day

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

javed.ghazal@gmail.com09811810454

Outcome results

None listed

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