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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03303027
Other study ID # 902404
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 27, 2016
Est. completion date April 16, 2019

Study information

Verified date April 2019
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Traditionally, dermatologic surgeons close wounds with stitches. Fast absorbing gut is a dissolvable stitch that is very commonly used. Some surgeons believe that using a thinner size of this stitch causes less skin reaction and improves the cosmetic outcome of the scar. Other surgeons believe that using a thicker size of this stitch reduces the tension on the scar and improves the cosmetic outcome of the scar in that manner. The investigator wishes to determine whether the thickness of the fast absorbing gut suture that is used makes a difference in the cosmetic outcome of the scar.


Description:

The purpose of this study is to determine whether the use of 6-0 fast absorbing gut during repair of linear cutaneous surgery wounds on the face or neck improves scar cosmesis compared to wound closure with 5-0 fast absorbing gut. The investigator will use a split wound model, where half of the wound is repaired with 6-0 fast absorbing gut and the other half is repaired with 5-0 fast absorbing gut. Three-months post-surgery, the scar will be measured via the patient observer scar assessment scale, a validated scar instrument. The scar width, and adverse events will also be recorded.

This study aims to investigate whether 5-0 versus 6-0 fast absorbing gut suture leads to better surgical wound cosmesis on the head and neck. The 5-0 fast absorbing gut suture has a large diameter, and therefore greater tensile strength. The greater tensile strength would provide better support of the healing scar during the first 5-7 days after surgery and for this reason, could potentially lead to improved scar cosmesis. However, the greater diameter could also lead to track marks that are larger and more visible. Furthermore, fast absorbing gut has a high degree of tissue reactivity to begin with, and it is known that larger diameter sutures generate more tissue reactivity compared to smaller diameter sutures of the same material; therefore, it is also possible that the 6-0 fast absorbing gut suture would provide better scar cosmesis by virtue of its lower tissue reactivity3,4.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 16, 2019
Est. primary completion date March 21, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older

- Able to give informed consent themselves

- Patient scheduled for cutaneous surgical procedure on the head and neck with predicted primary closure

- Willing to return for follow up visit.

Exclusion Criteria:

- Mentally handicapped

- Unable to understand written and oral English

- Incarceration

- Under 18 years of age

- Pregnant Women

- Wounds with predicted closure length less than 3 cm

Study Design


Intervention

Device:
6-0 fast absorbing gut suture
Fast absorbing surgical gut suture is a strand of collagenous material, size 6-0
5-0 fast absorbing gut suture
Fast absorbing surgical gut suture is a strand of collagenous material, size 5-0

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of California, Davis

References & Publications (4)

Gabrielli F, Potenza C, Puddu P, Sera F, Masini C, Abeni D. Suture materials and other factors associated with tissue reactivity, infection, and wound dehiscence among plastic surgery outpatients. Plast Reconstr Surg. 2001 Jan;107(1):38-45. — View Citation

Hochberg J, Meyer KM, Marion MD. Suture choice and other methods of skin closure. Surg Clin North Am. 2009 Jun;89(3):627-41. doi: 10.1016/j.suc.2009.03.001. Review. — View Citation

Tajirian AL, Goldberg DJ. A review of sutures and other skin closure materials. J Cosmet Laser Ther. 2010 Dec;12(6):296-302. doi: 10.3109/14764172.2010.538413. Review. — View Citation

van Rijssel EJ, Brand R, Admiraal C, Smit I, Trimbos JB. Tissue reaction and surgical knots: the effect of suture size, knot configuration, and knot volume. Obstet Gynecol. 1989 Jul;74(1):64-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Scar Assessment The primary endpoint will be the score of two blinded reviewers using the patient observer scar assessment score at a three-month assessment visit. 3 months following the procedure
Secondary Width of the Scar The secondary endpoints will include the width of the scar 1 cm from midline on each side at the follow-up visit and any complications from the treatment. 3 months following the procedure