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Comparing the therapeutic effect of cervix cryotherapy with and without nobothian cyst drainage in the treatment of women with chronic cervicitis

Comparing the therapeutic effect of cervix cryotherapy with and without nobothian cyst drainage in the treatment of women with chronic cervicitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022821653N4
Enrollment
144
Registered
2017-03-10
Start date
2015-06-25
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

chronic cervicitis. Inflammatory disease of cervix uteri

Interventions

Intervention 1: Interventional group one, cryotherapy without nabothian cyst drainage. Intervention 2: Interventional group two, cryotherapy is done after nobothian cyst drainage with needle 5 cc
Treatment - Surgery
Interventional group one, cryotherapy without nabothian cyst drainage
Interventional group two, cryotherapy is done after nobothian cyst drainage with needle 5 cc in controlled and healthy procedure

Sponsors

Vice chancellor for research, Jahrom University of Medical Sience
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria included a married woman who has a child and enters the study after knowing all aspects of the study with satisfaction. Exclusion criteria included the presence of certain immune deficiency diseases, especially cancers of the reproductive system and non-existence of the patient satisfaction for entering the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hypogastric pain. Timepoint: Visiting the patient once a month for three months after intervention. Method of measurement: check list, patients expression.;Dysuria. Timepoint: Visiting the patient once a month for three months after intervention. Method of measurement: check list, patients expression.;Dyspareunia. Timepoint: Visiting the patient once a month for three months after intervention. Method of measurement: check list, patients expression.;Green or yellow vaginal discharge. Timepoint: Visiting the patient once a month for three months after intervention. Method of measurement: check list, vaginal examination.;Bleeding after intercourse. Timepoint: Visiting the patient once a month for three months after intervention. Method of measurement: check list, patients expression.;Mucopurulent vaginal discharge. Timepoint: Visiting the patient once a month for three months after intervention. Method of measurement: check list, vaginal examination.

Secondary

MeasureTime frame
Cervix stenosis. Timepoint: once a month for three months. Method of measurement: check list, vaginal examination.;Uterus adhesion. Timepoint: visting the pateint once a month for three months. Method of measurement: check list, sonography.;Uterus prolapse. Timepoint: visting the pateint once a month for three months. Method of measurement: check list, vaginal examination.;Spotting. Timepoint: visting the pateint once a month for three months. Method of measurement: check list, patients expression.;Hypogastric pain. Timepoint: visting the pateint once a month for three months. Method of measurement: check list, patients expression.;Infertility. Timepoint: once a month for three months. Method of measurement: check list, patients follow up.;Idiopathic abortion. Timepoint: visting the pateint once a month for three months. Method of measurement: check list, patients follow up.;Making a mistake in diagnosis with ectropion or tissue damage. Timepoint: visting the pateint once a month for three months. Method of measurement: check list, patients follow up.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDoctor kavous Solhjo

Jahrom University of Medical Sience

sohjo@jums.ac.ir+98 79 1334 0406

Outcome results

None listed

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