Trials / Completed
CompletedNCT03530150
Pirfenidone and Its Role in Burn Wound Healing
Pirfenidone and Its Efficacy in Wound Re-Epithelization in Patients With Second-Degree Burns: A Proof-of-Concept Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 8 (actual)
- Sponsor
- Universidad Autonoma de Nuevo Leon · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
Burn patients which skin has been lost a rapid growth of the skin is a foremost in their treatment. Due to the injury, burn patients undergo a systemic inflammation that helps the skin heal faster. However, several studies have shown that this inflammation increases the levels of several inflammatory molecules that impairs skin growing, which further delays the recovery of burn patients. As such, by inhibiting these inflammatory molecules with the administration of a medication called pirfenidone burn patients might present faster rates of skin growth and recovery. Thus, patients suffering from a burn injury will be recruited at the emergency department of the Hospital University in Monterrey Mexico. Afterward, patients will be randomized to either receive pirfenidone 600 mg orally once per day or usual care consisting of covering the wound with hydrocolloid dressings. To assess the amount of newly growth skin investigators will take a small piece of the skin to further evaluate it through a microscope.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Pirfenidone Oral Product | A pill containing 600 mg of pirfenidone |
Timeline
- Start date
- 2017-01-01
- Primary completion
- 2017-06-22
- Completion
- 2017-06-22
- First posted
- 2018-05-21
- Last updated
- 2018-05-21
Source: ClinicalTrials.gov record NCT03530150. Inclusion in this directory is not an endorsement.