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Evaluation intrauterine adhesion after uterine myoma surgery

Intrauterine synechiae after myomectomy; laparotomy versus laparoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014123020486N1
Enrollment
40
Registered
2015-02-15
Start date
2013-07-06
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

intrauterine synechia. Other specified noninflammatory disorders of uterus

Interventions

Intervention 1: All patients in intervention group underwent myomectomy by laparoscopy method. Surgeries were performed in the follicular phase of menstrual cycle (except for those with metrorrhagia).
if there was any, the patient would excluded of the survey. The myomectomy surgical technique was similar by control group (laparotomy). For uterine suturing, the 1 and 0 vicryl suture was used. In th
if there was any, the patient would excluded of the survey. The myomectomy surgical technique was similar by intervention group (laparoscopy). For uterine suturing, the 1 and 0 vicryl suture was used.
Treatment - Surgery
All patients in intervention group underwent myomectomy by laparoscopy method. Surgeries were performed in the follicular phase of menstrual cycle (except for those with metrorrhagia). Surgery was pe
All patients in control group underwent myomectomy by laparotomy method. Surgeries were performed in the follicular phase of menstrual cycle (except for those with metrorrhagia). Surgery was performe

Sponsors

Research Deputy of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
16 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all of the married fertile women who had undergone myomectomy; having intra-mural and sub-serosal fibroids; types 3-6 (according to FIGO classification). Exclusion criteria: receiving GnRH analogous; a history of uterine surgery; the presence of systemic conditions which increase the occurrence rate of synechiae such as genital tuberculosis, endometritis or post-operative fever of unknown origin; no desire to includr in the survey; patients for whom laparoscopy was contra-indicated due to the myoma size or other parameters.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intrauterine synechia. Timepoint: 3 months after myomectomy. Method of measurement: According to the modified classification of the European Society of Gynecological Endoscopy (ESGE).

Secondary

MeasureTime frame
Evaluation relationship between type, size and location of myoma with frequency and severity of intrauterine adhesion. Timepoint: 3 months after myomectomy. Method of measurement: Based on FIGO classification.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Asgari

Tehran University of Medical Sciences

dr.zahra.asgari@gmail.com+98 21 7773 3934

Outcome results

None listed

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