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A comparative study to evaluate the insertion of postpartum intrauterine contraceptive device with the new inserter versus Kelly forceps .

A prospective, interventional, comparative study to evaluate the insertion of postpartum intrauterine contraceptive device using the dedicated inserter versus Kelly forceps. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072917
Enrollment
60
Registered
2024-08-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: O909- Complication of the puerperium, unspecified

Interventions

Intervention1: Dedicated inserter . : Insertion of contraceptive device with dedicated inserter which is long and does not need a specific instrument . Duration -Follow up after 6 weeks . Frequency -

Sponsors

Dr Palak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Primiparous or multiparous women delivering vaginally and willing for long term reversible contraception.(Including instrumental deliveries ) 2 Consenting and willing for Copper T IUD. 3 Patients who fulfil the WHO Medical eligibility criteria for contraceptive use 4 Insertion within 48 hours following delivery.

Exclusion criteria

Exclusion criteria: 1 women not willing to participate 2 women with pelvic inflammatory disease 3 cesarean delivery 4 peri partum fever 5 women with anaemia , thrombocytopenia 6 women with postpartum haemorrhage 7 women with chorioamnionitis

Design outcomes

Primary

MeasureTime frame
1 To assess the correct fundal placement of PPIUCD in the uterus. 2 To assess provider’s satisfaction in terms of ease of insertion using five- point LIKERT scale. Timepoint: Immediately after insertion and at 6 weeks postpartum.

Secondary

MeasureTime frame
1 To assess patients’ satisfaction and perception of pain using three-point LIKERT scale. 2 Confirmation of PPIUCD retention by a six-week follow-up. Timepoint: 6 weeks post partum

Countries

India

Contacts

Public ContactDr Vanita jain

Postgraduate institute of medical education and research, Chandigarh

drvanitajain@yahoo.com9914209352

Outcome results

None listed

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