Chlamydia trachomatis by Transcription‑Mediated Amplification (TMA)
Also known as: CTAMD
Use
Qualitative detection of Chlamydia trachomatis RNA using a nucleic acid amplification method. This assay provides sensitive, specific identification of infection and is intended for medical diagnostic use.
Special Instructions
Change effective as of 01/05/26: refer to 3020542 in the January Immediate Change Hotline.
Limitations
This test does not include confirmation of positive results by an alternative nucleic acid target. It is not valid for forensic purposes. For confirmation, see CT/NG TMA with reflex to confirmation assay. Not validated for evaluation of suspected sexual abuse.
New York Approved
Methodology
Other
Biomarkers
LOINC Codes
- 43304‑5
Result Turnaround Time
1-4 days
Related Documents
For more information, please review the documents below
Specimen
Vaginal Swab
Volume
Not provided
Minimum Volume
Not provided
Container
Aptima MultiTest Swab Specimen Collection kit (pink swab)
Collection Instructions
Vaginal swab collected with Aptima MultiTest Swab Specimen Collection kit (ARUP supply #65761 single or #55224 pack)
Storage Instructions
Refrigerated
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 2 months |
| Refrigerated | 2 months |
| Frozen | 1 year |