Comparing Liquid Vaseline and Olive Oil for Itching and Scarring in Scald Burns
Comparison of the Effects of Liquid Vaseline and Olive Oil on Itching and Scarring in Scald Burns
This study is testing whether liquid Vaseline or olive oil can help reduce itching and scarring in adults with second-degree scald burns.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 24 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Ankara Yildirim Beyazıt University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06104540 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effects of liquid petroleum jelly and olive oil on itching and scarring in patients with second-degree scald burns. Participants aged 18-65 with a total body burn area of less than 15% will be randomly assigned to receive either liquid vaseline, olive oil, or no treatment. The study aims to assess symptom relief, including itching and hypertrophic scarring, which are common complications following burn injuries. By comparing these two moisturizing agents, the research seeks to provide evidence-based recommendations for post-burn care.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 with less than 15% total body area affected by second-degree scald burns who have completed their treatment.
Not a fit: Patients with burns on the face and neck, those with dermatologic diseases, or individuals using antihistamines may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide effective, low-cost treatments to alleviate itching and scarring in burn patients, improving their quality of life.
How similar studies have performed: While there is limited scientific evidence on the effects of olive oil and liquid petroleum jelly for this specific application, the study aims to fill a gap in existing literature.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Between the ages of 18-65, * With a total body burn area of less than 15% 2nd degree scald burn, * Wwhose treatment has been completed and who do not need dressing and do not have open wounds, * Who do not have any allergies, * Who can read and write, * Who do not have cognitive problems, * Who do not have communication problems, * Who live in Ankara and who volunteer to participate in the study. Exclusion Criteria: * Patients with burns on the face and neck, * Ppatients with dermatologic diseases and patients using antihistamines will not be included. * Patients who do not want to continue the study, * Who develop an allergic reaction during the follow-up period, * Who start treatment during the follow-up period due to itching, * Wwho have not applied more than 20% liquid vaseline/olive oil during the 3-month follow-up period (60 applications/30 days; more than 36 applications out of 180 applications) will be excluded from the study.
Where this trial is running
Ankara
- Ankara Bilkent City Hospital — Ankara, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Merve AKIN, Ass Prof — Ankara City Hospital Bilkent
- Study coordinator: Nuray Çetintaş
- Email: nuray-2111@hotmail.com
- Phone: 905462651755
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.