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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03143114
Other study ID # WR3
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 15, 2017
Est. completion date June 15, 2021

Study information

Verified date August 2020
Source Mansoura University
Contact Waleed El-refaie, Dr
Phone +201224515318
Email wrefaie@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the effect of myomectomy for intramural myomas on the fertility outcomes in infertile women.


Description:

All women participating in the study will be randomly allocated into two groups; myomectomy group and conservative management group. Women in the myomectomy group will be subjected to laparotomy to remove the myomas while women in the conservative management group will not be subjected to surgery. Women in the myomectomy group will be asked to abstain from having sexual intercourse (or use a barrier contraception method) for 3 months after surgery then to start having regular fertility-oriented intercourse after that. Women in the conservative management group will be asked to immediately start having regular fertility-oriented intercourse. Women in both groups will be monitored form the time of starting regular intercourse and for one year for occurrence of clinical pregnancy.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date June 15, 2021
Est. primary completion date June 15, 2021
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 33 Years
Eligibility Inclusion Criteria:

- Infertility for at least one year.

- Presence of intramural myoma.

- Absence of any other cause of infertility as revealed by basic infertility work up including laparoscopy.

Exclusion Criteria:

- Age is < 20 or > 33 years.

- Symptomatic fibroid causing pelviabdominal swelling.

- Presence of > 2 myomas.

- Presence of a coexisting another type of myoma other than intramural myoma (e.g. submucosal, subserosal, cervical or ligamentary myoma).

- Presence of any other cause of infertility.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Myomectomy
Laparotomy then incision in the uterine wall to remove the myoma followed by closure of the uterine incision

Locations

Country Name City State
Egypt Obstetrics and Gynecology Department in Mansoura University Hospital Mansourah Dakahlia
Egypt Obstetrics and Gynecology Department in Mansoura University Port Said

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rate Number of clinical pregnancies (defined as presence of at least one intrauterine gestational sac with fetal pole and cardiac activity on TVS scan at 6-8 weeks gestational age) divided by the number of women 6-8 weeks gestational age
Secondary Miscarriage rate Number of first trimester miscarriages (before 12 weeks gestational age) divided by the number of clinical pregnancies 12 weeks gestational age
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