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A Comparative Study of Camphor Extract and Povidone-Iodine for Surgical Skin Cleaning.

In Vitro and Randomized Controlled Clinical Trial Assessing the Efficacy of Hydro-Alcoholic Camphor Extract Compared to Povidone-Iodine for Surgical Skin Preparation.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104123
Enrollment
100
Registered
2026-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

None listed

Sponsors

Parul institute of ayurved
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 years and above undergoing clean or clean-contaminated elective surgical procedures. Patients willing to participate and provide written informed consent. Patients undergoing minor elective surgical procedures such as hernia repair, circumcision, hydrocele repair,excision of cysts,lipoma,skin tags,warts,nail avulsion,and ear lobe repair. Patients of either gender irrespective of religion,occupation,or socio-economic status. Patients with normal preoperative laboratory investigations.

Exclusion criteria

Exclusion criteria: Known hypersensitivity or allergy to camphor,alcohol,or povidone-iodine. Patients with active skin infections or dermatological conditions at the surgical site eczema,dermatitis,cellulitis. Immunocompromised patients including those on chronic steroid therapy, chemotherapy, or with systemic immunodeficiency. Patients positive for HIV,HBsAg,orVDRL. Patients suffering from uncontrolled diabetes mellitus,malignancy,burns,leprosy,syphilis,or osteomyelitis. Patients unwilling to give informed consent.

Design outcomes

Primary

MeasureTime frame
Mean reduction in Colony Forming Units (CFU/cm ) from pre-application of hydroalcoholic camphor extract compared with povidone-iodine in patients undergoing clean elective surgerieTimepoint: 4 days

Secondary

MeasureTime frame
Incidence and severity of local skin reactions burning, itching, redness assessed using graded scoring scale post-application. Incidence of allergic or hypersensitivity reactions assessed through preapplication patch testTimepoint: 4 days

Countries

India

Contacts

Public ContactMAURYA AKANSHA SUBHASHCHANDR

Parul institute Ayurveda

hemant.toshikhane@paruluniversity.ac.in8469496525

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026