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To Study the Effect of Karnapurana in the Patient of Tinnitus

A Comparative Clinical Study To Evaluate The Therapeutic Effect Of Karnapurana With Lashun Siddha Moorchit Sarshap Tail And Moorchit Sarshap Tail In Karnanada W.S.R. To Tinnitus. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085979
Enrollment
50
Registered
2025-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: H833- Noise effects on inner ear

Interventions

None listed

Sponsors

Parul Institute Of Ayurveda And Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 18-75 years. Clinical diagnosis of subjective tinnitus. Participants with moderate to severe tinnitus as assessed by a validated tinnitus severity scale (Tinnitus Handicap Inventory, Tinnitus Functional Index). Stable general health with no acute systemic illness or active ear infections. Absence of prior ear surgery or invasive procedures affecting auditory function. Absence of known allergy to garlic or mustard to ensure safety of oil application. Willing and able to comply with study procedures and follow-up visits.

Exclusion criteria

Exclusion criteria: Objective tinnitus or structural auditory abnormalities. Severe otological or neurological disorders. Current use of tinnitus-altering medications. Significant psychiatric disorders. Pregnancy or lactation. Ear infections or inflammation. Allergies to intervention. Other medical or social factors impacting participation. Tinnitus from earwax, foreign bodies, or tympanic membrane rupture.

Design outcomes

Primary

MeasureTime frame
Reduces the severity of tinnitus.Timepoint: 0-15 days BT-0th Day DT-7th Day AT-15th Day

Secondary

MeasureTime frame
Improvement in Tinnitus Severity (Subjective Perception),Quality of Life,Changes in Sleep Quality,Reduction in Anxiety and Depression Symptoms,Etc.Timepoint: 0-15 days BT-0th Day DT-7th Day AT-15th Day

Countries

India

Contacts

Public ContactDr Ganesh Tejasvi S

Parul Institute of Ayurveda and Research, Parul University, Vadodara, Gujarat

ganesh.s36117@paruluniversity.ac.in9164774710

Outcome results

None listed

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