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Effect of Pranic Healing as addâ??on therapy in chronic rhinosinusitis

Evaluating the Impact of Pranic Healing as a Complementary Therapy on Physical, Functional, and Emotional Outcomes in Chronic Rhinosinusitis without Nasal Polyp: A Mixed Method Study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075679
Enrollment
76
Registered
2024-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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: Conventional Treatment + Pranic Healing: Oxymetazoline Nasal drops 2-2-2 drops X 5 days T. Amoxicillin with clavulanic acid 625mg, 1-0-1 X 5 days T. Paracetamol+ Chlorpheniramine male

Sponsors

World Pranic Healing Foundation India - Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Those who consent to participate in the study 2. Both male and female subjects aged 18 years to 65 years 3. Those who were diagnosed with chronic rhinosinusitis without nasal polyp with at least two of the symptoms (a) nasal blockage/obstruction/congestion, (b) nasal discharge (anterior or posterior), (c) facial pain or pressure, or (d) reduction or loss of smell. 4. Subjects with moderate to severe symptoms indicated by SNOT -22 scores ranging from 21 -100

Exclusion criteria

Exclusion criteria: Subjects with positive skin prick test indicating atopy Subjects with abnormal spirometry results Subjects who require surgical management within 2 months Subjects with nasal tumors, acute sinusitis, allergic fungal rhinosinusitis, allergic rhinitis Subjects with uncontrolled diabetes mellitus Subjects with severe hepatic and renal disease, and other severe medical conditions requiring immediate intervention. Subjects with skin diseases such as eczema, urticaria, skin rashes Lund Mackay CT scores more than 14 Subjects who are on corticosteroids Subjects with a history of epistaxis due to secondary cause Subjects who are cognitively impaired and unable to provide reliable symptom ratings. Subjects who are pregnant or lactating. Subjects who are not willing to participate Subjects who are participating in any other clinical or interventional study

Design outcomes

Primary

MeasureTime frame
Change in SNOT -22 scores and Change in Pittsburgh Sleep Quality Index scoresTimepoint: 0, 4 Weeks

Secondary

MeasureTime frame
Change in SNOT -22 scoresTimepoint: 2 weeks and Telephonic follow up 6 weeks;Improvement in nasal airflow and nasal patencyTimepoint: 0, 4 Weeks;Pranic Healing Experience Questionnaire (PEPQ) â?? Qualitative narrativeTimepoint: 2, 4 weeks and Telephonic follow up 6 weeks

Countries

India

Contacts

Public ContactSrikanth Jois Nagaraja

Darlas Health Care

entsowmya@gmail.com9741805003

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 9, 2026