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CODEPAD (Collaborative Outcomes of DEpression and Pain Associated With Delivery)

Active Not RecruitingPhase 2, Phase 3

Sponsor: KK Women's and Children's Hospital

Conditions: Depression, Postpartum, Analgesia, Obstetrical, Anesthesia, Obstetrical

Interventions: Epidural delivery system, Entonox, Meperidine, Ultiva, Fentanyl

Countries: Singapore

Postnatal depression affects about 10-15% of women after childbirth. Approximately 3-5% of women experience a moderate-to-severe depression that requires medical attention. This study aims to investigate the implication of pain relief choice in reducing the postnatal depression of women who deliver their babies.

Eligibility overview

Sex: FEMALE

Age: 21 Years to 50 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* Healthy adult (American Society of Anesthesiologists physical status 1 and 2) parturients at term (36 weeks gestation or more) (nulliparous and multiparous);
* With a singleton fetus.

Exclusion Criteria:

* Multiple pregnancies;
* Non-cephalic fetal presentation;
* Obstetric complications (e.g. pre-eclampsia, uncontrolled hypertension, uncontrolled diabetes);
* Elective and urgent caesarean section (not from delivery suite).

Locations (1)

Singapore, Singapore