Comparison of the Effect of Vaseline and Bepanthen® "Wund- Und Heilsalbe" on the Wound Healing Following Laser Therapy

Photodamaged Skin Clinical Trial

— CO2  

Official title:

Comparison of the Effect of Vaseline and Bepanthen® "Wund- Und Heilsalbe" on the Wound Healing Following Fractional Ablative Laser Treatment of Photo-damaged Skin

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03095872
• Other study ID #: 16-011
• Status: Completed
• Phase: Phase 3
• Start date: March 1, 2017
• Est. completion date: February 5, 2018

Study information

• Verified date: May 2018
• Source: RWTH Aachen University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In the field of dermatology the healing process and therefore the success of a laser treatment are strongly determined by an appropriate postoperative treatment of the laser-treated skin. The manufacturer of CO2 laser systems recommends the application of Vaseline postoperatively to protect the treated tissue from air exposition until encrustation of the laser-treated skin decreases (usually after 7-14 days). An alternative to Vaseline could be Bepanthen® "Wund- und Heilsalbe" (Bayer). It contains the active ingredient pro-vitamin Dexapanthenol, which is widely used in dermatology therapy. The product helps to stabilize the protective barrier of the skin, to reduce the skin irritation, to stimulate the skin regeneration and to promote the wound healing. In an in-vitro study Bepanthen® "Wund- und Heilsalbe" triggered wound closure significantly faster compared to Vaseline. In this study the effect of Bepanthen® "Wund- und Heilsalbe" on wound healing should be investigated and compared to Vaseline in vivo following fractional ablative CO2 laser treatment of photo-damaged skin.

Description:

The healing process and therefore the success of a laser treatment are strongly determined by an appropriate treatment with special skin care products of the laser-treated skin. Cooling measures prevent the swelling of the treated skin area, if applied directly after the procedure. A soothing and wound-healing-promoting care applied subsequently for seven days, can support and also speed up the healing process.

The Lumenis® Company is the manufacturer of CO2 laser systems and recommends the application of the Okklusiv ointment Vaseline® postoperatively, in order to prevent the treated tissue to the air exposition. These occlusive wound care should be maintained, until the encrustation of the laser-treated skin decreases, which usually happens 7-14 days postoperatively.

The Bepanthen® Wund- und Heilsalbe (Bayer) could be a possible alternative to Vaseline® as postoperative care. Bepanthen® Wund- und Heilsalbe contains pro-vitamin Dexpanthenol as an active ingredient and is widely used in dermatological therapy. The product helps to stabilize the protective barrier of the skin, to reduce the skin irritation, to stimulate the skin regeneration and to promote the wound healing. The investigators examined the effect of substances containing Dexpanthenol on wound healing process applied topically, in three-dimensional (3D) dermal skin equivalents in vitro. For this purpose, many lesions with standardized diameter and depth were generated using a laser. The subsequent topical application of substances containing dexpanthenol on the wound healing models (treated with laser) for three-days led to a significantly faster wound closure compared to Vaseline-covered models (Marquardt et al., 2015). The aim of this study is to compare the effect of white Vaseline with Bepanthen® "Wund- und Heilsalbe" (both applied postoperatively) on the wound healing following fractional ablative CO2 laser treatment of photo-damaged skin in vivo.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 37
• Est. completion date: February 5, 2018
• Est. primary completion date: January 22, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years

• photodamaged skin, which need to be treated with the fractional ablative CO2 laser

Exclusion Criteria:

• pregnant or lactating females

• chronic diseases such as diabetes and vascular disease with impaired wound healing

• Patients, who tend to form hypertrophic scars and keloids

• Patients, who take the isotretinoin-containing medication in the past year

• topical or systemic corticosteroid treatment

• immunocompromised patients

• Patients with the Koebner phenomenon

• People with the skin type 6

• Patients with melanoma

Related Conditions & MeSH terms

• Photodamaged Skin

Intervention

Device:
• CO2-laser
Patients with photo-damaged skin are treated with the CO2 laser to remove damaged skin layers.

Drug:
• Vaseline
After the laser treatment, the wound area will be divided into two parts with a sterile skin marker. One area will be treated with Vaseline, and be marked "V". Thus, it is ensured that the care product will be applied correctly to the defined area. Postoperatively, this area of the wound will be treated with Vaseline. In the next seven days the patient will repeat the treatment every day at home.
• Bepanthen
After the laser treatment, the wound area will be divided into two parts with a sterile skin marker. One area will be treated with Bepanthen® Wund- und Heilsalbe, and be marked "B". Thus, it is ensured that the care product will be applied correctly to the defined area. Postoperatively, this area of the wound will be treated with Bepanthen® Wund- und Heilsalbe. In the next seven days the patient will repeat the treatment every day at home.

Locations

Country	Name	City	State
Germany	University Hospital RWTH Aachen	Aachen	NRW

Sponsors (1)

Lead Sponsor	Collaborator
RWTH Aachen University

Country where clinical trial is conducted

Germany, 

References & Publications (4)

Bogdan Allemann I, Kaufman J. Laser principles. Curr Probl Dermatol. 2011;42:7-23. doi: 10.1159/000328236. Epub 2011 Aug 16. — View Citation

Marquardt Y, Amann PM, Heise R, Czaja K, Steiner T, Merk HF, Skazik-Voogt C, Baron JM. Characterization of a novel standardized human three-dimensional skin wound healing model using non-sequential fractional ultrapulsed CO2 laser treatments. Lasers Surg Med. 2015 Mar;47(3):257-65. doi: 10.1002/lsm.22341. Epub 2015 Mar 15. — View Citation

Reinholz M, Tietze JK, Kilian K, Schaller M, Schöfer H, Lehmann P, Zierhut M, Klövekorn W, Ruzicka T, Schauber J. Rosacea - S1 guideline. J Dtsch Dermatol Ges. 2013 Aug;11(8):768-80; 768-79. doi: 10.1111/ddg.12101. Epub 2013 May 6. English, German. — View Citation

Wigger-Alberti W, Kuhlmann M, Ekanayake S, Wilhelm D. Using a novel wound model to investigate the healing properties of products for superficial wounds. J Wound Care. 2009 Mar;18(3):123-28, 131. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of the diameter of the individual lesions [initial value 1.3mm] between study visits.	Large clinical digital photos as well as dermatoscopic images of the skin.	Over 2 weeks (immediately after laser treatment and on day 1, 2, 5 and 14 after laser treatment)
Primary	Change of the size of the individual lesions between study visits.	Two-dimensional microscopic skin cut images in real time of the skin.	Over 2 weeks (immediately after laser treatment and on day 1, 2, 5 and 14 after laser treatment)
Primary	Visual changes of the wound healing between study visits.	The wound healing rates will be visually assessed, based on the measure of re-epithelialization.	Over 2 weeks (immediately after laser treatment and on day 1, 2, 5 and 14 after laser treatment)
Primary	Change of the wound under cosmetic aspects between study visits.	The cosmetic result is based on a visual analog scale (VAS) from 0 (bad) to 10 (excellent, with no visible difference of the wound to the surrounding tissue).	Over 2 weeks (immediately after laser treatment and on day 1, 2, 5 and 14 after laser treatment)
Secondary	Change of the transepidermal water loss (TEWL) between study visits.	TEWL is the most important parameter for the assessment of skin barrier function.	Over 2 weeks (immediately after laser treatment and on day 1, 2, 5 and 14 after laser treatment)

External Links

•   Leitlinie zur Behandlung der aktinischen Keratosen C44.X der Deutschen Dermatologischen Gesellschaft.