Evaluation of diagnostic accuracy and side effects of endometrial biopsy curette
Not Applicable
Recruiting
- Conditions
- terine endometrial biopsy.Malignant neoplasm of uterus, part unspecified
- Registration Number
- IRCT20151120025139N2
- Lead Sponsor
- Salamat yar Hakim Engineering Company
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Age range 75-18
Willingness to participate in the study
Exclusion Criteria
History of endometrial cancer
History of atypical endometrial hyperplasia
Positive pregnancy test result
Reluctance to participate
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pathological outcome. Timepoint: 10 days after biopsy. Method of measurement: Pathological evaluation.;Patients' pain intensity. Timepoint: Immediately after sampling. Method of measurement: Observation and questioning of the patient.;Complications after biopsy. Timepoint: After sampling. Method of measurement: Observe symptoms in the patient.
- Secondary Outcome Measures
Name Time Method