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Status unknownNCT02335476Updated Oct 14, 2016

Automatic Early Melanoma Detection by Ultrahigh Resolution Three Dimensional Optical Coherence Tomography

An observational study in Melanoma, sponsored by National Taiwan University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2016-10-14.

Sponsored by National Taiwan University Hospital · Observational

The sponsor has not verified this record recently (last verified Oct 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Enrollment
100
Ages
20 Years and older
Sex
All
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Study summary

The investigators will use optical coherence tomography to detect the ex-vivo tissue image of surgical removed melanoma or other benign pigmented lesions of skin.

Read the detailed description

The investigators will use an advanced high resolution 3D optical coherence tomography (OCT) technology to observe skin tissue images in ex vivo culture. Parts of melanoma or benign pigmented lesions specimens derived from biopsy or surgical excision specimen will be observed by 3D optical tomography. A tiny tissue fragment of melanoma or benign pigmented lesions will be taken from surgical specimen without interference normal pathological evaluation. The location of melanocytic cells in melanoma or benign tissue fragments will be mapped by the 3D optical coherence tomography (OCT). The 3D optic tomography system utilize a Ce:YAG optical fiber as light source and also combined with confocal microscopy. Taken together, these features made the 3D optic tomography system have very high resolution and suitable for single cell imaging. This study will not interfere with the normal medical practice and had no impact on patient's safety and health. All of the materials will be destroyed once the experiments are done. The enrollment criteria will be dermatological patients who need to surgical intervention.

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Conditions studied

  • Melanoma

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Keywords

  • optical coherence tomography
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In context

Melanoma

3,006 studies on the registry are indexed under Melanoma; 520 are open to participants now.

This study's planned enrollment of 100 is below the median of 182 across 438 observational studies indexed under Melanoma.

Browse Melanoma studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

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

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Who can participate

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

Study population

Participants are patients at out-patient clinics or ward of Department of Dermatology, National Taiwan University Hospital.

Inclusion criteria

  • Patients aged older than 20 years old
  • Patients who had melanoma, melanoma in situ, and/or other benign pigmented lesions,
  • Patients who had non-melanoma skin cancers (basal cell carcinoma, or squamous cell carcinoma).
  • Patients who had precancerous skin lesions (Bowen's disease, actinicc keratosis)

Exclusion criteria

Exclusion Criteria:

  • Pregnant women.
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Study design

Enrollment
100 participants (estimated)
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What researchers measure

Primary outcomes

  1. Ex vivo Tissue image.

    Partial fragments of tissue specimens from melanoma, melanoma in situ, or other benign pigmented lesions will be used for imaging purpose by a optical coherence tomography.

    Time frame: 1 day

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Study locations

1 of 1 sites recruiting
  • National Taiwan University Hospital
    Taipei City, 10016, Taiwan
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 14, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02335476
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Jan 9, 2015
Start date
Mar 2015
Primary completion
Apr 2017 (estimated)
Completion
Apr 2017 (estimated)
Last update
Oct 14, 2016

Study contacts

JENGWEI TJIU
Contact
jengweitjiu@gmail.com
886-2-23123456 ext. 65315
JENGWEI TJIU
principal investigator · National Taiwan University Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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