Skip to content

Topical Preparation Containing Andrographis paniculata Extract in Normal Healthy Volunteers

Topical Preparation Containing Andrographis paniculata Extract in Normal Healthy Volunteers

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250714003
Enrollment
20
Registered
2025-07-14
Start date
2024-10-01
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

Researchers developed a novel topical product containing A. paniculata extract for easier application to burn wounds

Interventions

Four test sites of upper arm (right anterior, right posterior, left anterior, and left posterior upper arms) were identified on each participant. Four creams were randomly applied, one to each site :c
Cream base,Topical preparation containing 5% A. paniculata extraction,silver sulfadiazine,Topical preparation containing 10% A. paniculata extraction

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: healthy volunteers aged 18 to 65 years and the ability to follow study instructions

Exclusion criteria

Exclusion criteria: known pregnancy or breastfeeding, Andrographis allergy, bleeding disorders, use of anticoagulants or antiplatelets, drugs affecting cytochrome P450, immunosuppressive medications, or the presence of wounds at the test site.

Design outcomes

Primary

MeasureTime frame
Allergic reaction assessment following day 3 and 7 at 7 days s after end of the intervention Friedman test to assess differences among groups, while changes in allergic reactions over time were analyzed using the Wilcoxon Signed Ranks Test

Secondary

MeasureTime frame
level of iching at 7 days after end of the intervention Friedman test to assess differences among groups, while changes in allergic reactions over time were analyzed using the Wilcoxon Signed Ranks Test,User Satisfaction after end of the intervention ANOVA or pair T-test

Countries

Thailand

Contacts

Public ContactSuphat Watthanathiranon

Division of surgery, Faculty of Medicine Siriraj Hospital

suphatwat@gmail.com0643599915

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026