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Analgesic Effect And Safety Of Topical Sevoflurane During Dressing Of Painful Wound

Analgesic Effectiveness And Safety Of Topical Sevoflurane During Dressing/Debridement Of Painful Ulcer/Wound

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034481
Enrollment
100
Registered
2021-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: L99- Other disorders of skin and subcutaneous tissue in diseases classified elsewhere

Interventions

Intervention1: Topical Sevoflurane: 1ml/cm2 7-10min over wound Control Intervention1: Placebo: Alternate dressing without Topical Sevoflurane

Sponsors

Dr Ajin Anto AK
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: visual analogue score >4 while wound dressing. the wound etiology maybe arterial, venous, lymphatic or traumatic.

Exclusion criteria

Exclusion criteria: pregnant and lactating women. Patient with cognitive and senile dementia. Neuropathic and painless wound.

Design outcomes

Primary

MeasureTime frame
painless wound dressingTimepoint: one and half year—

Secondary

MeasureTime frame
1)rashes if sevoflurane come in contact with skin. So sevoflurane drop is placed over wound bed without coming contact with skin.Timepoint: Maximum duration 1day—

Countries

India

Contacts

Public ContactDr Ajin Anto AK

Command Hospital Airforce Bangalore

viveksadhnaom@gmail.com9596078989

Outcome results

None listed

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