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Register:	ClinicalTrials.gov
Last refreshed on:	12 December 2020
Main ID:	NCT02995356
Date of registration:	12/12/2016
Prospective Registration:	No
Primary sponsor:	Ege University
Public title:	Evaluation of the Axonemal Dynein Heavy Chain 5 and Creatine Kinase Concentration in Cervical Fluid for Early Detection of the Ectopic Pregnancy
Scientific title:
Date of first enrolment:	September 2016
Target sample size:	85
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT02995356
Study type:	Observational
Study design:
Phase:

Countries of recruitment
Turkey

Contacts

Key inclusion & exclusion criteria

Inclusion Criteria:

- Doubted ectopic pregnancy

- Without any finding about intrauterine pregnancy in ultrasonography results

- Without any vaginal bleeding

- Having irregular pregnancy test results

- Beta-HCG results should be at least upper than 100 milli-International unit (mIU/ml)

- Having fist trimester pregnancy for intrauterine pregnancy group

- Without any emergency findings

Exclusion Criteria:

- Doubted incomplete abortion

- Having vaginal bleeding

- Having ultrasound results which include intrauterine embryo report

- Having lower than 100 mIU/ml beta-HCG results

- Without fetal heart rate in intrauterine pregnancy group

- Having older than fist trimester pregnancy for intrauterine pregnancy group

- Having emergency findings

Age minimum: 18 Years
Age maximum: 45 Years
Gender: Female

Health Condition(s) or Problem(s) studied

Ectopic Pregnancy

Intervention(s)

Other: Collecting cervical liquid and sera samples

Primary Outcome(s)

Concentration of creatine kinase [Time Frame: 1 year]

Concentration of Axonemal Dynein Heavy Chain 5 [Time Frame: 1 year]

Secondary Outcome(s)

Secondary ID(s)

2.101.2015.0076

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:
Date Posted:
Date Completed:
URL:

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