Evaluation of postpartum depression in patients undergoing cesarean section managed with an ERAS protocol

Effect of ERAS protocol after cesarean section on postpartum depression: a randomized controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN16339153

Enrollment

150

Registered

2025-12-29

Start date

2025-04-01

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

Evaluation of postpartum depression following ERAS implementation in patients undergoing cesarean section. Pregnancy and Childbirth

Interventions

Methods Study Design This study was designed as a prospective randomized controlled trial conducted in the Department of Obstetrics and Gynecology. The anticipated study duration is nine months. Par

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Patients with indications for cesarean section 2. 18-40 age pregnant woman 3. Without a prior diagnosis of psychiatric illness and without current or previous use of psychiatric medications

Exclusion criteria

Exclusion criteria: 1. Presence of preeclampsia or eclampsia 2. Pre-existing hypertension 3. Placental invasion anomalies 4. Placental abruption 5. Pregestational or gestational diabetes mellitus 6. Perioperative complications (including intraoperative bladder or bowel injury) 7. Orthopedic conditions that could limit postoperative mobilization

Countries

Türkiye

Contacts

Public ContactTansu Bahar Gürbüz

tansu.gurbuz@iuc.edu.tr+90 05325479464

Outcome results

None listed

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