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Comparison of Papsmear adequacy with either Ayrespatula and Cervix brush

Comparison of Papsmear adequacy with either Ayrespatula and Cervix brush in patients reffered to a private medical office,2007-2008

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201206131306N4
Enrollment
198
Registered
2012-07-10
Start date
2007-07-09
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Comparison of Papsmear adequacy with either Ayrespatula and Cervix brush. Provisional assignment of new diseases of uncertain etiology

Interventions

Intervention 1: use Ayre spatula in first group. Intervention 2: use Cervix Brush in second group.
Diagnosis
use Ayre spatula in first group
use Cervix Brush in second group

Sponsors

Vice Chancellor for research – Guilan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

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

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026