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A Study to Evaluate How Effectively Amrutveni LiceQit Oil Treats Head Lice Infestation in Children and Adults.

An Open-Label, Single-Arm, Interventional Clinical Test to Evaluate the Efficacy of Amrutveni LiceQit oil in Reducing Head Lice and Nit Count - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096413
Enrollment
36
Registered
2025-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: B850- Pediculosis due to Pediculus humanus capitis

Interventions

Intervention1: Amrutveni LiceQit oil: Type of Product: Herbal topical formulation (cosmeceutical / therapeutic oil) Dosage Form: Oil (for external application on scalp and hair) Route of Administrat

Sponsors

Sahyadri Bio Labs Pvt. Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals aged between 18 and 60 years Presence of head Lice infestation

Exclusion criteria

Exclusion criteria: Known hypersensitivity or allergy to any ingredients present in the Amrutveni LiceQit Oil. Presence of underlying dermatological scalp disorders such as psoriasis, seborrheic dermatitis, or eczema. Use of other anti-lice treatments or pediculicides within the preceding 7 days. Participation in any other clinical test within the past 30 days. Pregnant or lactating women, due to unknown effects on maternal or neonatal health.

Design outcomes

Primary

MeasureTime frame
Mean percentage reduction in live lice and nit count from baseline (Day 0) to Day 28, determined by standardized lice detection combing and count comparisonTimepoint: Day 0 (baseline), Day 1–7, Day 14, Day 21, and Day 28

Secondary

MeasureTime frame
1. Change in Pediculosis Severity Score (PSS) from Day 0 to Day 28. 2. Change in itching intensity (VAS, 0–10). 3. Change in scalp inflammation/redness (0–3 scale). 4. Improvement in hair texture, softness, and manageability. 5. Change in hair volume and tangle score. 6. Overall subject satisfaction (1–5 Likert scale). 7. Incidence of local irritation, erythema, allergic reaction, and overall safety (IGDES score). Timepoint: Day 0 (baseline), Day 1–7, Day 14, Day 21, and Day 28

Countries

India

Contacts

Public ContactDr Kasthuri Nair A

Pankajakasthuri Ayurveda Medical college and PG centre

dr.kasthurinair@pkhil.com8113851665

Outcome results

None listed

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