← Eichor
Study identifier: NCT07258459 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Two Previous Cesarean and Vaginal Birth Before and After Starting Training and Protocols

Condition: Cesarean Delivery Affecting Fetus or Newborn · Labor (Obstetrics)--Complications · Hemorrhagic Complications  ·  Sponsor: G. d'Annunzio University

PhaseN/A
Planned participants2016
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

In 2015 ObGyn Dept of Santo Spirito Hospital in Pescara (Italy) started protocol for previous CS vaginal birth. In 2021 was started a protocol for training on obstetric emergencies and protocol on two previous cesarean was endorsed. Patients attending birth in Pescara with two previous from january 2016 to December 2020, and from january 2021 to december 2025 were collected. A different counseling approach was adopted from 2021. Women's acceptance of trial of labor and maternal and fetal outcomes were collected.

This description comes directly from the study's public registry record.

Talk to the study team

Claudio Celentano, MD  ·  +39 328 5577305  ·  celentanoclaudio70@gmail.com

Always discuss trial participation with your own doctor first.

Locations (2)

Claudio CelentanoPescara, PE, ItalyRecruiting
Santo Spirito HospitalPescara, PE, ItalyRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07258459