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Surgical versus medical treatment for abnormal uterine bleeding in premenopausal women

Surgical versus medical treatment for abnormal uterine bleeding in premenopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103065563N3
Enrollment
97
Registered
2011-03-24
Start date
2007-05-13
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: diphereline 3.75 mg IM every 28 days for 3 doses. Intervention 2: standard surgical treatment (abdominal hysterectomy).
Treatment - Drugs
Treatment - Surgery
diphereline 3.75 mg IM every 28 days for 3 doses
standard surgical treatment (abdominal hysterectomy)

Sponsors

Vice Chancellor for Research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Premenopausal women between 40-55 years old with abnormal uterine bleeding for at least 2 months which is described as bleeding more than 7 days in a month or heavy bleeding resulting in anemia (Hct<32%), no evidence for atypical heperplasia or carcinoma in D&C, no response to simple medications such as medroxy progetrone and contraceptive tablets, no Ovarian or uterine organic lesions (ruled out by using clinical examination and ultrasonography) Exclusion criteria: Anemia for other reasons, Fertility preservation, Evidence of pregnancy, Endocrinopathy, Coagulopathy, contraindications for medical treatment, Using IUD

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Uterine bleeding. Timepoint: before intervention, 2, 3 months and 2 years after intervention. Method of measurement: asking from patient.

Secondary

MeasureTime frame
Anemia. Timepoint: before intervention, 2, 3 months and 2 years after intervention. Method of measurement: Hb and Hct analysis.;Quality of life. Timepoint: before intervention, 2, 3 months and 2 years after intervention. Method of measurement: WHOOQL standard questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElaheh Ouladsahebmadarek

Tabriz University of Medical Sciences

elmadarek33@yahoo.comadarek@tbzmed.ac.ir+98 41 1553 9160

Outcome results

None listed

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