Thymol Dressing in Diabetic foot Ulcer

Evaluation of Safety and Efficacy of Hydropolymer Dressing (Hydrogel) with Thymol for the Treatment of Neuropatic Diabetic Foot Ulcer in a Phase I/II Clinical Trail

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20170612034485N3

Enrollment

Registered

2018-12-30

Start date

2018-08-06

Completion date

Unknown

Last updated

2019-01-14

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

Conditions

Chronic neuropathic diabetic foot Ulcer. Type 2 diabetes mellitus with foot ulcer

Interventions

Intervention group: in this group, the patients will use thymol-honey (Herbaderm) dressing on their granulated wound daily. the dressing will be changed every 24 hours..

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Chronic neuropathic diabetic foot ulcer (more than 6 weeks) with wound classification Wagner I & II Full informed consent for recruitment in the study Age between 18-70 years

Exclusion criteria

Exclusion criteria: Suspected osteomyelitis Using corticosteroid or immunosuppressor drug Chronic renal failure and hemodialysis

Design outcomes

Primary

Measure	Time frame
Local and systemic side-effects. Timepoint: Every month up to month 6th (or complete healing). Method of measurement: Clinical examination.;Complete wound healing during study (at least 6 months). Timepoint: Every month up to month 6th. Method of measurement: Clinical examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Esmaeeli Djavid

Iranian academic center for education culture and research

djavid@ut.ac.ir+98 21 6698 9110

Outcome results

None listed

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