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Treatment of throat infection with Unani medicine Habb-e-Khardal

Clinical validation of Unani Pharmacopoeial formulation Habb-e-Khardal in Waram-e-Halaq (Pharyngitis) - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071434
Enrollment
300
Registered
2024-07-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: J312- Chronic pharyngitis

Interventions

Intervention1: Habb-e-Khardal: 500 mg (two tablets of 250mg) to be taken orally with water twice daily one hour after meals for 14 days. Control Intervention1: NIL: NIL

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex in the age group of 18-60 years. 2. Patients having Sore throat Pharyngeal Inflammation along with any of these Cough Rhinorrhoea Hoarseness Oral ulcers Conjunctivitis

Exclusion criteria

Exclusion criteria: 1. Age below 18 and more than 60. 2. Patient with GERD. 3. Patient having bacterial pharyngitis. 4. Fever more than 100 F 5. Weak debilitating patients 6. Known cases of other clinically significant co-morbid conditions (severe hepatitis, renal, cardiovascular disorders, etc.) that in the opinion of the investigator could affect the efficacy and safety outcome of the study. 7. Patients with laboratory values outside the normal limits or those with values considered abnormal in the opinion of the investigator 8. Known hypersensitivity to study drug or any of its ingredients. 9. Pregnancy and lactation 10. Any Malignancy 11. History of alcohol and drug abuse.

Design outcomes

Primary

MeasureTime frame
The efficacy of the study drug will be assessed on the basis Sore throat questionnaireTimepoint: At baseline, 14th day and 21 day of treatment.

Secondary

MeasureTime frame
Haematological & biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examination.Timepoint: At baseline and after 14days

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

ghazala.javed@gov.in9811810454

Outcome results

None listed

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