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 sites396 target enrollmentTBD

Overview

Phase: Phase 1
Intervention: Not specified
Conditions: Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Sponsor: ALL INDIA INSTITUTE OF MEDICAL SCIENCES JODHPUR
Enrollment: 396
Status: Not yet recruiting
Last Updated: 4 years ago

No summary available.

Registry

who.int

Start Date

TBD

End Date

December 28, 2021

Last Updated

4 years ago

Study Type

Interventional

Sponsor

ALL INDIA INSTITUTE OF MEDICAL SCIENCES JODHPUR

•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.