â??Comparison of the expulsion rate of intra uterine contraceptive device Cu T 375 and Copper T 380 A after post placental and early postpartum insertion- A randomized control trialâ??

ALL INDIA INSTITUTE OF MEDICAL SCIENCES JODHPUR0 个研究点目标入组 396 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•1.All Postpartum women delivering in our institute either vaginally or by caesarean section who fulfills the medical eligibility criteria for Cu T insertion (10).
•2.Those women consenting to participate in the study and willing to come for follow up

•1.Women with history of Sexually transmitted diseases or pelvic inflammatory diseases, coagulation disorders, liver or renal dysfunction, Diabetes Mellitus or Wilsons disease.
•2.Intrapartum and recent antepartum fever (within 7 days), puerperal sepsis, postpartum haemorrhage, rupture of membranes for greater than 18 hours prior to delivery.
•3.Women with pre-existing gynecological cancers
•4.Women with uterine anomalies or leiomyoma distorting the shape of uterine cavity.
•5.Previous 2 LSCS
•6.Patients not giving consent.

发起方

ALL INDIA INSTITUTE OF MEDICAL SCIENCES JODHPUR