Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04812275
Other study ID # 2020-06004
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 19, 2021
Est. completion date November 11, 2023

Study information

Verified date December 2023
Source Department of Hand surgery Södersjukhuset
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

After all surgical procedures, the skin must be closed with some form of stitch, in healthcare called suture. According to the tradition of hand surgery, sutures that must be removed by caregivers, ie non-resorbable thread, have been used extensively, and the frequency of complications in the form of wound rupture and infection is low. For many procedures, however, it can be an advantage to avoid removing the stitches, as it is both painful for the patient and time-consuming and resource-consuming for both the patient and the healthcare system. You can then use a thread that the body itself breaks down and absorbs, ie resorbable suture. In the project, we will compare resorbable and non-resorbable suture with the primary outcome of superficial infection in the surgical area sometime day 1-20 after surgery. Secondary outcomes are the occurrence of wound rupture, pain VAS (Visual Analog Scale) when changing 2 weeks postoperatively, patient satisfaction VAS at 2 weeks and time spent in minutes for changing at 2 weeks postoperatively. The project will include all consecutive patients> 18 years of age who are operated on at the hand surgery clinic Södersjukhuset for elective or emergency surgery that do not meet the exclusion criteria. The project will include 270 patients.


Recruitment information / eligibility

Status Completed
Enrollment 270
Est. completion date November 11, 2023
Est. primary completion date November 10, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - all consecutive patients> 18 years of age who are operated on at the hand surgery clinic Södersjukhuset for elective or emergency surgery that do not meet any of the exclusion criteria. Exclusion Criteria: - -The researcher has an age <18 years. - Patients with known healing problems in the past, for example patients with burns or during cortisone treatment. - Patients undergoing surgery where skin grafting occurs. - Patients with acute injuries that include a traumatic wound-ie what is usually referred to as "open injuries" -where the risk of infection is higher from the beginning.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Skin closure
Skin closure

Locations

Country Name City State
Sweden Södersjukhuset Hospital Stockholm

Sponsors (1)

Lead Sponsor Collaborator
Department of Hand surgery Södersjukhuset

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Infection Signs of superficial infection after surgery. Redness, pus, swelling. 2 weeks
Secondary Rupture The prevalens of wound rupture after hand surgery 2 weeks
Secondary VAS Visual analog scale 2 weeks
Secondary Time Time consumption removal of sutures 2 weeks