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Treatment of abnormal uterine bleeding

Comparison of two kinds of treatment with thermal balloon and hysteroscopy in the treatment of abnormal uterine bleeding

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201207163820N5
Enrollment
70
Registered
2012-08-18
Start date
2011-11-09
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

Abnormal uterine bleeding. Other specified abnormal uterine and vaginal bleeding

Interventions

Intervention 1: Frist group:treatment with tharmal balloon, Intervention group. Intervention 2: Second group:treatment with hysteroscop, control group.
Treatment - Surgery
Frist group:treatment with tharmal balloon, Intervention group
Second group:treatment with hysteroscop, control group

Sponsors

Vice Chancellor for Research and technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1 - no response to treatment; 2 - lack of desire for fertility and having children; 3 - normal cervical cytology; 4 - normal endometrial histology. Exclusion criteria: 1 - intrauterine pathologies (such as polyps or submocusal fibroma); 2 - Uterine cavity length more than 12 cm; 3 - hyperplasia or endometrial atypy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The amount of vaginal bleeding. Timepoint: 6 month and 12 month. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Perforation of the uterus after treatment. Timepoint: Intraoperative. Method of measurement: Clinical.;Uterine infection after treatment. Timepoint: 7-3 days after intervention. Method of measurement: Clinical.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDR. Zinatossadat Bouzari

Babol University of Medical Sciences

z_b412003@yahoo.com+98 11 1223 8301

Outcome results

None listed

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