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Benefits of Unani medicine in common cold

A Comparative clinical study on the efficacy of Laooq shamoon vs Laooq khiyarshambar in Allergic Rhinitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053622
Enrollment
28
Registered
2023-06-07
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: J309- Allergic rhinitis, unspecified

Interventions

Intervention1: LAOOQ SHAMOON: Asl-us-soos nimkofta Glycyrrhiza glabra L. 20gms 2. Maghz-e-Behidana Cydonia oblonga Mill. 20gms 3. Tukhmekhashkhashsafaid Papaver somniferum L. 40gms 4. Samagh-e-arbi Ac

Sponsors

National Institute of Unani Medicine Bangalore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age between 18-60 years 2. All genders 3. All cases of allergic rhinitis according to ARIA classification 4. Subjects with both intermittent and/or persistent allergic rhinitis and having at least two of the following rhinitis-associated conditions: nasal congestion, rhinorrhea, sneezing and nasal itching. 5. Patients who will give consent and able to do follow up

Exclusion criteria

Exclusion criteria: 1. Subjects having Nasal polyps, Sinusitis, Atrophic rhinitis, Hypertrophied turbinates,Deviated nasal septum, and congenital nasal abnormalities like nasal dermoid cysts, congenital midline nasal masses etc. 2. Subjects with a history of heart diseases, kidney diseases, liver diseases, DM,Malignancy, and severe asthma. 3. Subjects who had received systematically or topically administered corticosteroids, antihistamines, or decongestants 07 days prior to enrolment 4. Personnel who are taking part in other clinical trials 5. Subjects with known allergy from the ingredients of trial interventions 6. Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
Reduction in Rhino-conjunctivitis Total Symptom Score (RCTSS)Timepoint: 4 weeks

Secondary

MeasureTime frame
1.Reduction in SNOT-22 score 2.Improvement in subjective parameters 3. AECTimepoint: 4 WEEKS

Countries

India

Contacts

Public ContactDr Mohd Riyazuddin

National institute of unani medicine bangalore

shaikh.riyaz368@gmail.com8010392768

Outcome results

None listed

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