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CONTRACEPTION WITH COPPER-T IMMEDIATELY FOLLOWING CHILD BIRTH

IMMEDIATE POSTPARTUM INTRAUTERINE CONTRACEPTIVE DEVICE INSERTION

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/08/001933
Enrollment
30
Registered
2011-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Intra-uterine contraceptive device (copper-T 380A): Intra-uterine contraceptive device (copper-T 380A) to be inserted in immediate postpartum period, i.e. in vaginal delivery after deli

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: females of reproductive age were selected in immediate postpartum period Incidence(i.e. immediately following delivery of placenta, intracaesarean or within 48 hours after delivery of baby)

Exclusion criteria

Exclusion criteria: prolonged rupture of membrane18 hr unresolved postpartum haemorrhage distorted uterus extensive genital trauma trophoblastic disease AIDS

Design outcomes

Primary

MeasureTime frame
non-expulsion of intra-uterine contraceptive deviceTimepoint: patients will be followed up for 3 months after insertion—

Secondary

MeasureTime frame
NoneTimepoint: N/A—

Countries

India

Contacts

Public ContactJhuma Biswas
drjhumabiswas@yahoo.in03322041352

Outcome results

None listed

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