ClinicalTrials.gg
RecruitingNCT05785182Updated Oct 2, 2026

OCT in Open Fracture and Infected Fracture

An observational study in Trauma Injury, Trauma and Open Fracture, sponsored by Dartmouth-Hitchcock Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-02.

Sponsored by Dartmouth-Hitchcock Medical Center · Observational

From the registry’s dates

  • Started Mar 2023; still recruiting 3 years 7 months later.
Updated Oct 2, 2026Primary completion movedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years and older
Sex
All
01

Study summary

This is a pilot prospective, observational study of patients with open or infected fracture evaluating the feasibility and acceptability of OCT, a light-based imaging modality that requires no drug or contrast agent.

02

Conditions studied

  • Trauma Injury
  • Trauma
  • Open Fracture
  • Fracture Infection
03

In context

Accidental Injuries

128 studies on the registry are indexed under Accidental Injuries; 39 are open to participants now.

This study's planned enrollment of 40 is below the median of 170 across 59 observational studies indexed under Accidental Injuries.

Browse Accidental Injuries studies →

Lead sponsor

Dartmouth-Hitchcock Medical Center is the lead sponsor of 488 studies on the registry; 71 are open to participants now.

Of its 31 completed or terminated interventional studies of FDA-regulated products, 21 (68%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients 18 years of age or older who present to DHMC (Lebanon) with open and infected fracture

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

  • Age 18 years or older
  • Open fracture
  • Fracture Related Infection

Exclusion criteria

Exclusion Criteria:

  • Metatarsal fractures
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No

Groups and cohorts

  • Open Fracture

    High energy open fracture.

    Procedure: Open Fracture

  • Infected Fracture

    Infected open or closed fracture.

    Procedure: Infected Fracture

Interventions

  • ProcedureOpen Fracture

    Patients 18 years of age or older with open fracture. Provision of informed consent.

  • ProcedureInfected Fracture

    Patients 18 years of age or older with infected fracture. Provision of informed consent.

06

What researchers measure

Primary outcomes

  1. Feasibility and acceptability of OCT imaging

    The primary objective of this work is to demonstrate feasibility, acceptability, and preliminary effectiveness of Optical Coherence Tomography (OCT) to image bacteria and biofilm. Data will be analyzed accordingly: The association between optical imaging parameters (particularly around biofilm and bacterial contamination) and (1) surgical wound severity and (2) development of infection or treatment failure for infection.

    Time frame: 36 months

07

Study locations

1 of 1 sites recruiting
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Mar 2023 to primary completion in Jul 2026, 40 months.

Of 33 non-industry observational studies under Accidental Injuries, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 60. This study's 40 months is above that.

Counting every sponsor, half of 39 studies reached it within 31 months; a quarter within 12 and three quarters within 60.

Primary completion moved once since we started tracking on Sep 25, 2026: Aug 2026 → Jul 2026, on Oct 2, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Mar 14, 2023
First posted
Mar 27, 2023
StartActual
Mar 27, 2023
Primary completionActual
Jul 28, 2026was Aug 2026
CompletionEst.
Jun 2027
Last update
Oct 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Primary completion
Aug 2026→Jul 28, 2026 (actual)
Oct 2, 2026
Show all 1 update
  1. Oct 2, 2026
    Primary completion Aug 2026→Jul 28, 2026 (now actual)

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 ↗

09

Registry details

Key details

Study ID
NCT05785182
Collaborators
Dartmouth College
Responsible party
Ida Leah Gitajn (Section Chief, Orthopaedics, Dartmouth-Hitchcock Medical Center) — Principal investigator
First posted
Mar 27, 2023
Start date
Mar 27, 2023
Primary completion
Jul 28, 2026
Completion
Jun 2027 (estimated)
Last update
Oct 2, 2026

Study contacts

Holly B Symonds
Contact
Holly.B.Symonds@hitchcock.org
603-653-9440
Devin S Mullin
Contact
Devin.S.Mullin@hitchcock.org
603-650-6032
Ida L Gitajn
principal investigator · Dartmouth-Hitchcock Medical Center

Oversight

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

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