Salpingectomy During Cesarean Section

NAUnknownINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

September 30, 2016

Primary Completion Date

July 31, 2018

Study Completion Date

July 31, 2018

Conditions
Healthy
Interventions
PROCEDURE

tubal ligation group II

"Every woman , who is eligible to enter the study in terms of the above criteria , will receive a detailed explanation of the study and will review the consent form , and then be asked whether she agrees to participate in . If so , the participant will stamped on the informed consent form .~The control group will be women who undergo tubal ligation method BTL during cesarean section . All women will be invited to follow up about three months after surgery. The women will answer questionnaire to quantify the symptoms of menopause by NAMS , blood test for AMH and sonar and Doppler examination of both the ovaries"

PROCEDURE

salpingectomy group I

women who agreed to participate in the study and assigned randomly to this group will have salpingectomy during cesarean section for sterilization.

Trial Locations (1)

31048

ISRAEL, Haifa

Sponsors
All Listed Sponsors
lead

Bnai Zion Medical Center

OTHER_GOV