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OpenTrials
Completed

NCT Number: NCT04812275

Absorbable or Non Absorbable Sutures in Hand Surgery

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.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Södersjukhuset Hospital

Stockholm, 118 83, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Skin closure

Procedure

Skin closure

Primary outcomes

  1. Infection

    Time frame: 2 weeks

    Signs of superficial infection after surgery. Redness, pus, swelling.

Secondary outcomes

  1. Rupture

    Time frame: 2 weeks

    The prevalens of wound rupture after hand surgery

  2. VAS

    Time frame: 2 weeks

    Visual analog scale

  3. Time

    Time frame: 2 weeks

    Time consumption removal of sutures

Sponsors and collaborators

Lead sponsor

Department of Hand surgery Södersjukhuset

Other

Registry information

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Mar 23, 2021
Registry last updated
Dec 15, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.