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Uterine fluid lactate dehydrogenase isoenzyme activity profile. Can it be considered a diagnostic marker for endometrial cancer?

Uterine fluid lactate dehydrogenase isoenzyme activity profile. Can it be considered a diagnostic marker for endometrial cancer? A prospective controlled clinical trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000135617
Enrollment
200
Registered
2014-02-05
Start date
2014-02-08
Completion date
2014-05-15
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

A new test for diagnosis and early detection of endometrial cancer

Interventions

200 Postmenopausal women with one or more episode of vaginal bleeding will be included after signing informed consent. The transvaginal ultrasonography (TVS ) and uterine fluid sampling for lactate dehydrogenase ( LD ) isoenzyme analysis will be performed as office examinations taking about 30 minutes on the same setting. Endometrial thickness will be classified as >5 mm or <5 mm on TVS. Patients with endometrial thickness >5 mm on TVS will be evaluated with diagnostic curettage, and tho

200 Postmenopausal women with one or more episode of vaginal bleeding will be included after signing informed consent. The transvaginal ultrasonography (TVS ) and uterine fluid sampling for lactate dehydrogenase ( LD ) isoenzyme analysis will be performed as office examinations taking about 30 minutes on the same setting. Endometrial thickness will be classified as >5 mm or <5 mm on TVS. Patients with endometrial thickness >5 mm on TVS will be evaluated with diagnostic curettage, and those with endometrial thickness <5 mm will be evaluated with office endometrial biopsy usually within one week . LD isoenzyme profile will subsequently be related to histopathological diagnosis.

Sponsors

alexandria univerisity
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
45 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

females with postmenopausal uterine bleeding even one episode of bleeding will be included in the study

Exclusion criteria

Patients with recent endometrial sampling. Current hormone replacement therapy Uterine fluid collection at TVS Clinical signs of endometritis

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026