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NCT02941198
Postpartum Immediate Contraception in Cesarean Deliveries-Comparison of Two Intrauterine Systems
NA trial testing GyneFix in Intrauterine Systems in 140 participants. Completed in 31 January 2017.
31 January 2017
Quick facts
| Lead sponsor | Zeynep Kamil Maternity and Pediatric Research and Training Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 140 |
| Start date | 1 June 2016 |
| Primary completion | 31 January 2017 |
| Estimated completion | 31 January 2017 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- GyneFix
- Cu T380 A
Conditions studied
- Intrauterine Systems — all drugs for Intrauterine Systems →
- Postpartum Immediate Contraception — all drugs for Postpartum Immediate Contraception →
Sponsor
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Who can join
Adults 18 to 50, female only, with Intrauterine Systems or Postpartum Immediate Contraception. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To compare two intrauterine systems in order to avoid complications originating from short pregnancy interval and undesired pregnancies in the early postpartum period.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT02941198
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Intrauterine Systems
Currently open trials in the same condition.
- NCT07382583 — Development of a Shared Decision Tool to Facilitate Uptake of the Levonorgestrel-releasing Intrauterine System for the P · recruiting
Other Zeynep Kamil Maternity and Pediatric Research and Training Hospital trials
Trials by the same sponsor.
- NCT05786352 — Outcomes of Enhanced Recovery After Cesarean (ERAC) Protocol · NA · unknown
- NCT07312617 — Short-Term Outcomes of TOT, TVT, and Burch Surgery Assessed by Transperineal Ultrasound · NA · completed
- NCT05558046 — Predictive Value of Granulosa Cell DNA Damage in the Success of Assisted Reproductive Technique · unknown
- NCT05558852 — Laparoscopic Central and Anterior Compartment Prolapse Surgery: A Meshless Sacrocolpopexy Technique · NA · unknown
- NCT04888091 — Comparison of the Effect of Cervical Mucus Cleaning Method Applied Before Embryo Transfer on Pregnancy Rates. · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02941198 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Zeynep Kamil Maternity and Pediatric Research and Training Hospital
- Last refreshed: 3 January 2018
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02941198.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing