Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: i) Subjects who are ready to give voluntary written informed consent. ii) Both Male and female subjects between the age group of 18-60years iii) Subjects who undergone any major/ minor surgeries where the surgical wound need a dressing will be taken in to the study
Exclusion criteria
Exclusion criteria: i) Subjects allergic to charcoal ii) Subjects who are unwilling to adhere to the study iii) Individual has a condition the Investigator believes would interfere with his or her ability to provide informed consent, comply with the study protocol, which might confound the interpretation of the study results or put the person at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| i) The primary objective of this pilot study is to assess the efficacy of DRONAID (activated charcoal absorption gauge) over surgical wound. ii) Pain if any during the dressing change at day 15Timepoint: i) The primary objective of this pilot study is to assess the efficacy of DRONAID (activated charcoal absorption gauge) over surgical wound at day 15 ii) Pain if any during the dressing change at day 15 | — |
Secondary
| Measure | Time frame |
|---|---|
| i) The secondary objective is to evaluate the time taken for complete wound healingTimepoint: Day 3,Day 6 and Day 15 | — |
Countries
India
Contacts
AIIMS Bhubaneswar