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OpenTrials
Completed

NCT Number: NCT01372488

Are Patients Willing and Capable of Removing Their Own Non-absorbable Sutures

1. Hypothesis

If patients who are sutured with non-absorbable sutures in the Emergency Department (ED) are provided with the proper equipment and knowledge on how to remove their own sutures, they will be willing and capable of removing their own sutures. 2. Primary and Secondary Questions

Primary Question What number of patients in the study group will successfully remove their own sutures if they are provided with the equipment and information on how to do so compared with a control group who are treated and advised in the usual fashion? (follow up with family doctor or local medical clinic for suture removal)

Secondary Questions

1. Number of complications related to self removal of sutures as compared to traditional treatment. Complications measured were wound infections, dehiscence and prolonged bleeding (>30 min) 2. Number of physician visits related to self removal of sutures as compared to traditional treatment. 3. Patient satisfaction and comfort level related to self removal of sutures as compared with traditional treatment.

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Key information

Conditions

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Royal Columbian and Eagle Ridge Hospitals

New Westminster, British Columbia, Canada

About this study

Introduction/Background:

Patients who are sutured with non-absorbable sutures in the Emergency Department are asked to follow up with their family doctor or local medical clinic for suture removal. Suture removal, especially for simple lacerations is easy to do. Given the proper instructions and equipment suture removal could be done by the patient or a family member.

Objectives:

Are patients willing and capable of removing their own non-absorbable sutures? How many patients can successfully self remove their own sutures if given the proper equipment and instructions as compared with patients who are not given equipment and instructions? Would patient self removal result in less physician visits related to sutured wounds? What would be the complication rate for self removal of sutures be? Specific complications were wound infection, dehiscence and prolonged bleeding? Would patients be satisfied and comfortable in taking out their own sutures?

Methods:

Patients who are sutured with non absorbable sutures in the emergency department will be randomly enrolled into either of two groups. One group will receive wound care instructions alone. The second group will be given wound care instructions, a suture removal kit and instructions regarding self-removal to take home. Both groups will be contacted by telephone 14 days after suturing and asked questions concerning who removed their sutures, number of physician visits, time loss from work related to suture removal and complications related to sutures or suture removal. Questions regarding patient satisfaction with respect to self removal of sutures will also be asked.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Patients 19 years and older that have wounds sutured in the ER with non-absorbable sutures

Exclusion criteria

  • Inability to give consent secondary to alcohol, drugs or failure to speak English
  • Complicated lacerations or lacerations which require close medical supervision
  • Lacerations that are inaccessible to the patient (ie. scalp, back or buttock lacerations)
  • Inability to contact patient by telephone for follow-up (no telephone, patient travelling out of country etc.)
  • Patients who are immunocompromised, have diabetes mellitus or are on steroid medications

Treatment and study plan

Suture self removal

Procedure

Suture self removal

Suture removal by family doctor or clinic

Procedure

As above

Primary outcomes

  1. Are patients willing and capable of removing their own non-absorbable sutures?

    Time frame: 3 months

    What number of patients in the study group will successfully remove their own sutures if they are provided with the equipment and information on how to do so compared with a control group who are treated and advised in the usual fashion? (follow up with family doctor or local medical clinic for suture removal)

Secondary outcomes

  1. Complications related to self removal of sutures

    Time frame: 3 months

    Number of complications related to self removal of sutures as compared to traditional treatment were measured. Complications measured were wound infections, dehiscence and prolonged bleeding (>30 min)

  2. Physician Visits Related to Suture Self Removal

    Time frame: 3 months

    Number of physician visits related to self removal of sutures as compared to traditional treatment.

  3. Patient Comfort and Satisfaction with Self-Removal of Sutures

    Time frame: 3 months

    Patient satisfaction and comfort level related to self removal of sutures as compared with traditional treatment. Measures used were a survey with a 5 choice answer.

Sponsors and collaborators

Lead sponsor

Fraser Health

Other

Collaborators

  • University of British Columbia

Registry information

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Jun 14, 2011
Registry last updated
Oct 12, 2021

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.