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

F

Fraser Health

Status

Completed

Conditions

Suture Removal

Treatments

Procedure: Suture removal by family doctor or clinic
Procedure: Suture self removal

Study type

Interventional

Funder types

Other

Identifiers

NCT01372488
2010-004

Details and patient eligibility

About

  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.

Full description

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.

Enrollment

160 patients

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

160 participants in 2 patient groups, including a placebo group

Study group
Active Comparator group
Description:
Study group will be provided with suture removal instructions and suture removal kit and asked to consider removing their own sutures
Treatment:
Procedure: Suture self removal
Control group
Placebo Comparator group
Description:
Control group will be asked to have their sutures removed as they normally would (see family doctor or clinic)
Treatment:
Procedure: Suture removal by family doctor or clinic

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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