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Post Marketing clinical study on surgical wound dressing

"An open label,comparative,post marketing study to evaluate the efficacy and safety of DRONAID dressing (activated charcoal absorption gauge) vs saline gauge used on surgical wound"

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/026207
Enrollment
50
Registered
2020-06-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: Carbon Surgical Bandages: DRONAID surgical wound dressing bandage is the medical device which will be used over the surgical wound as dressing material.The dressing will be applied till

Sponsors

Neosoteria Bandages Pvt Ltd
Lead Sponsor

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

MeasureTime 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

MeasureTime 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

Public ContactDr Tuhin Chakraborthy

AIIMS Bhubaneswar

surg_tushar@aiimsbhubaneswar.edu.in

Outcome results

None listed

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