Comparison of Papsmear adequacy with either Ayrespatula and Cervix brush

Phase 2

• Conditions: Comparison of Papsmear adequacy with either Ayrespatula and Cervix brush.; Provisional assignment of new diseases of uncertain etiology; U00-U49

• Registration Number: IRCT201206131306N4
• Lead Sponsor: Vice Chancellor for research – Guilan university of medical sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 198

Inclusion Criteria

Inclusion criterion: all patients who need to perform Pap smear.
Exclusion criteria: pregnant women who are under HRT and the patients with cervicitis.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Adeaquacy of pap smear in Ayre spatula and Cervix brush. Timepoint: Between menstrual cycle. Method of measurement: with Ayre spatula and Cervix brush.

Secondary Outcome Measures

Name	Time	Method
Adeaquacy of pap smear in Ayre spatula and Cervix brush by parity. Timepoint: Between menstrual cycle. Method of measurement: with Ayre spatula and Cervix brush.;Adeaquacy of pap smear in Ayre spatula and Cervix brush by Menopause. Timepoint: one year after Lack of menstruation. Method of measurement: with Ayre spatula and Cervix brush.;Adequacy of Causes of non-satisfactory in Ayre spatula and Cervix brush. Timepoint: Between menstrual cycle. Method of measurement: Based on presence or absence of an adequate endocervical cells.