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NCT06786156
Pregnant Women with Placenta Previa
EARLY_PHASE1 trial testing Pecha Kucha Education in Placental Previa in 90 participants. Not yet recruiting.
30 June 2025
Quick facts
| Lead sponsor | Burdur Mehmet Akif Ersoy University |
|---|---|
| Phase | EARLY_PHASE1 |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | supportive care |
| Enrollment | 90 |
| Start date | 1 February 2025 |
| Primary completion | 30 June 2025 |
| Estimated completion | 30 July 2025 |
Drugs / interventions tested
- Pecha Kucha Education
Conditions studied
- Placental Previa — all drugs for Placental Previa →
Sponsor
Burdur Mehmet Akif Ersoy University
Who can join
Adults 18 to 45, female only, with Placental Previa. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Placenta previa is the extension of placental tissue over the endocervical os or covering the cervical os. Placenta previa is a common complication in the third trimester of pregnancy and is a major cause of postpartum hemorrhage and perinatal death.There are many studies in the literature on attachment. However, no studies have been found on fetal movement in placenta previa pregnant women. Counting fetal movements is an easy and inexpensive assessment that pregnant women can do on their own, without the need for any specialist or equipment, and for which they take responsibility. It is assumed that the effective time spent during fetal movement counting will positively affect the attachment between the pregnant woman and the fetus, and that the stress of the pregnant woman, who is sure that her baby is well, will decrease.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06786156
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT06786156 (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 Burdur Mehmet Akif Ersoy University
- Last refreshed: 27 January 2025
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/NCT06786156.
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