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Comparative effectiveness of Itrifal ustukhuddus and Sharbat e Sadar in the treatment of Chronic Sinusitis

A clinical study of Waram Tajawif al -Anf Muzmin (chronic sinusitis) to evaluate the efficacy of ITRIFAL USTUKHUDDUS and SHARBAT E SADAR - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071703
Enrollment
60
Registered
2024-07-31
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: J329- Chronic sinusitis, unspecified

Interventions

Intervention1: Itrifal Ustukhuddus: Patients will be given compound test drug that has to be administered orally after meals in a dosage of 7gm for 6 weeks. Control Intervention1: Sharbat e Sadar: Pat

Sponsors

State Unani Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of any sex, aged 18-50 years 2. Duration of the disease greater than 12 week. 3. Patient having at least two out of four cardinal symptoms i.e., facial pain/pressure, hyposmia/anosmia, nasal obstruction, and nasal discharge for at least 12 consecutive weeks 4. Patient having any of the following symptoms like rhinorrhoea, nasal congestion, frontal headache, nasal itching, impaired sense of smell and frequent sneezing for more than 12 weeks. 5. Positive X-ray PNS finding like Thickened mucosal lining, opacity of sinus.

Exclusion criteria

Exclusion criteria: 1. Patient aged below 18 years or above 50 years 2. Patient with deviated nasal septum 3. Local pathology such as mucocele, cyst, antrochoanal polyp, facial trauma. 4. Diabetes mellitus and any other illness requiring long term treatment. 5. Pregnant or Lactating Women. 6. Significant Pulmonary/Cardiovascular/Hepato-renal Dysfunction 7. Known cases of Immunocompromised states like HIV/ AIDS, etc. or Malignancies 8. Patient not willing to attend regular treatment and follow-up for the entire duration of study 9. Mentally retarded patients. 10. Patient having history of any surgery of nose or paranasal sinuses. 11. Patient having history of trauma to nose or sinus area. 12. Patient of pulmonary Koch’s or having history of epistaxis. 13. Any medical condition where physician feels that participation in the study could be detrimental to patient’s well- being. 14. Alcoholic and Drug addicted patient.

Design outcomes

Primary

MeasureTime frame
Clinical assessment will be done and the response to treatment will be assessed using the following parameters: 1. Visual Analogue ScaleTimepoint: Week 2, 4 and 6.

Secondary

MeasureTime frame
1. Visual Analogue ScaleTimepoint: Week 2, 4 & 6.

Countries

India

Contacts

Public ContactDr Usamah Ahmad

State Unani Medical College

asifhussainusmani@gmail.com7905831926

Outcome results

None listed

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