Effectiveness of Pippalyadi Avapida Nasya followed by Anutaila Pratimarsha Nasya in Pratishyaya (Chronic Rhinosinusitis).

Randomized controlled clinical evaluation of Pippalyadi Avapida Nasya followed by Anutaila Pratimarsha Nasya in Pratishyaya with special reference to Chronic Rhinosinusitis. - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061049

Enrollment

132

Registered

2024-01-02

Start date

Unknown

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

Health Condition 1: J310- Chronic rhinitis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient who are willing to participate in the study and ready to give a written informed consent. 2. Subjects of either sex in the age group of 18 to 60 years. 3. Patients who are having the clinical signs and symptoms of Pratishyaya. 4. Patients fulfilling the criteria of chronic rhinosinusitis as per American Academy of Otolaryngology—Head and Neck Surgery (2015).

Exclusion criteria

Exclusion criteria: 1. Patient with migraine, tension type of headache, cluster headache, glaucoma or any other type of headache, except sinusitis. 2. Patients with space occupying lesion of brain. 3. Patients with nasal polyp, deviated nasal septum or any benign or malignant growth of nose and paranasal sinuses. 4. Known patient of epilepsy, mental disorder, malignancy, serious acute organic disease, or any serious comorbidity that will make it impossible to participate in the trial interventions. 5. Pregnant or lactating women. 6. Patients with contraindication of nasya karma.

Design outcomes

Primary

Measure	Time frame
1.Classical parameters of Pratishyaya 2. Sino-Nasal Outcome Test - 22 (SNOT-22) questionnaire score 3. Sino-Nasal Outcome Test - 20 (SNOT-20) questionnaire score 4. Sinus Control Test (SCT) 5.Haziness over the PNS (Maxillary sinuses) in X-Ray PNS water’s view 6.Haziness over the frontal sinuses in X-Ray Skull Caldwell view 7.Erythrocyte Sedimentation Rate (ESR) 8.C-Reactive Protein (CRP) Timepoint: Base line 15th day 30th day	—

Measure

Time frame

1.Classical parameters of Pratishyaya 2. Sino-Nasal Outcome Test - 22 (SNOT-22) questionnaire score 3. Sino-Nasal Outcome Test - 20 (SNOT-20) questionnaire score 4. Sinus Control Test (SCT) 5.Haziness over the PNS (Maxillary sinuses) in X-Ray PNS water’s view 6.Haziness over the frontal sinuses in X-Ray Skull Caldwell view 7.Erythrocyte Sedimentation Rate (ESR) 8.C-Reactive Protein (CRP) Timepoint: Base line 15th day 30th day

—

Secondary

Measure	Time frame
Adverse effect of the treatmentTimepoint: after treatment	—

Countries

India

Contacts

Public ContactVijay Kumar

North Eastern Institute of Ayurveda and Homoeopathy

drabhishekb@gmail.com8876059293

Outcome results