ClinicalTrials.gg
CompletedNCT07899684STITCHINGUpdated Oct 27, 2026

The Role of Simulation Fidelity in Early Surgical Skills Education

An interventional study of Suture skills retention in Medical Education, Simulation Training and Medical Student, sponsored by Medical University of Lodz. Completed at 3 sites in Poland. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Medical University of Lodz · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled May 2025, registered Oct 2026).
Updated Oct 27, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
131
Allocation
Randomized
Sex
All
01

Study summary

The aim of the study is to evaluate the effectiveness of teaching surgical suturing techniques using various materials (e.g., banana peel, orange peel, pork, chicken, and silicone pads). The study results will help identify the most effective teaching materials and methods, which will contribute to optimizing educational programs and improving the quality of training for future surgeons.

02

Conditions studied

  • Medical Education
  • Simulation Training
  • Medical Student
  • Medical Education Assessment

Keywords

  • surgical training
  • medical education
  • surgical suturing
  • surgery
03

In context

Lead sponsor

Medical University of Lodz is the lead sponsor of 107 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Medical students (any age and sex)
  • No prior experience in surgical suturing.
  • Written consent to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Medical students with prior experience in surgical suturing. Participation in specialized sewing courses outside the scope of the degree program.
  • Allergies to any of the materials used in the study.
  • Refusal to participate in the study.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
131 participants (actual)

Study arms

  • Active comparator
    Medical students (various materials)

    Medical students with no prior suturing experience and no known allergies to the materials used who are willing to participate in suturing on porcine skin, banana, chicken, or orange in Round 1, then on silicone model in Round 2.

    Procedure: Suture skills retention

  • Sham comparator
    Medical students (silicone only)

    Medical students with no prior suturing experience and no known allergies to the materials used who are willing to participate in suturing on a silicone model in Round 1, then on a silicone model in Round 2.

    Procedure: Suture skills retention

Interventions

  • ProcedureSuture skills retention

    Medical students with no prior formal experience in surgical suturing are randomly assigned to practice on one of five training materials using computer-generated randomisation: silicone pad, porcine skin, chicken tissue, banana peel or orange peel (study arm). All participants attend a lecture led by an experienced surgeon (academic teacher). After this, in Round 1, they practise suturing using a standardised protocol, supervised by experienced surgeons (four per group). In Round 2, trainees from all groups (silicone, porcine, chicken, banana, and orange) perform suturing on silicone pads (standardised material exposure, control arm). A pre-specified random subsample from each Round 1 arm are invited to Round 2 due to logistical constraints; selection is not performance-based. Consequently, if Round 2 has a smaller sample size than Round 1, and paired analyses of Round 1 and Round 2 would be performed only for participants with data available at both time points.

    Also known as: Skill retention

06

What researchers measure

Primary outcomes

  1. Trainee-reported outcomes

    Immediately after practice, trainees complete a questionnaire rating the training material and the learning experience. Four items are measured on a 5-point Likert scale (1-5): material comfort/usability, perceived realism (similarity to human skin), perceived understanding of basic suturing principles, and perceived development of practical skills. Additionally, trainees rate their confidence in placing sutures on a 0-10 numeric scale.

    Time frame: 1 day

  2. Expert-rated technical outcomes

    Experienced surgeons evaluate students' sutures across multiple domains, each scored on a 1-5 scale (1 = worst, 5 = best). For students who do not complete the task, a score of "0" is recorded, and the result is excluded from the qualitative analysis. Technical endpoints are analysed separately for simple interrupted domains, vertical mattress domains, and global composite scores, defined as the mean across available domains within a suture type. Composite scores will first be calculated at the participant level as the mean across available domains. Group-level summaries will be presented as medians with interquartile ranges (IQR) due to the non-normal distribution of scores.

    Time frame: 1 day

07

Study locations

3 sites
  • Department of General and Transplant Surgery, Medical University of Lodz, 22 Kopcińskiego St., 90-153 Łódź
    Lodz, PL 90-153, Poland
  • Department of Plastic, Reconstructive, and Aesthetic Surgery, Medical University of Lodz
    Lodz, PL, Poland
  • Department of Vascular, General, and Transplant Surgery, Wrocław Medical University
    Wroclaw, PL, Poland
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Yes

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07899684
Collaborators
Wroclaw Medical University
Responsible party
Sponsor
First posted
Oct 27, 2026
Start date
May 20, 2025
Primary completion
Nov 14, 2025
Completion
Nov 14, 2025
Last update
Oct 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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