RecruitingNCT06833788
Intravenous or oral iron after cesarean birth and postpartum depression
About this title
Read the official source — NCT06833788Medication studyAges 18+France
Understand this study
Who could participate?
Listed age limits: from 18 years.
What will I do during this study?
After a caesarean delivery, participants are randomly assigned to an iron infusion within five days or to oral iron for eight weeks. The study compares postpartum mood symptoms between these groups; the registry lists an assessment at eight weeks after delivery.
- Listed locations
- ParisSee all locations and recruitment
- Study phase
- Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
- Participation duration
- 8 weeks after delivery
What to know before participating
A point to clarify
This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?
Things to check before joining
Study start dateStarted: October 22, 2025
- Recruitment status
- Recruiting
- Enrollment listed in the registry
- 2,860
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- Unknown or unclear
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
- Locations
- France
- Age range
- Over 18 Years
- Official registry ID
- NCT06833788
- Official title
Show the full official title
Treatment of Anaemia After Caesarean With Intravenous Versus Oral Iron and Postpartum Depression: a Multicentric Randomized Open-labelled Controlled Trial
Recruitment & locations
RecruitingParis
A listed location does not confirm current availability.
Questions about this study
Who is behind this study?
The study sponsor is Assistance Publique - Hôpitaux de Paris.
Does this study involve medication?
Yes. The study involves medication, including Ferric carboxymaltose IV and TIMOFÉROL®.
Who can participate?
Listed age limits: from 18 years.
Is this study still recruiting?
The registry lists this study as recruiting.
