Overview

Ergot and Oxytocin During Cesarean Delivery Following Failure to Progress in Labour

Status:
Completed
Trial end date:
2007-01-01
Target enrollment:
0
Participant gender:
Female
Summary
Despite of marked improvements in clinical management, early postpartum hemorrhage(PPH)remains a significant contributor to maternal morbidity and mortality both in developing countries and in hospitals equipped with all that modern medicine has to offer. This complication is amongst the most challenging that a clinician will face in the obstetric patient. Prevention, early recognition and prompt appropriate intervention are the keys to minimizing the impact of PPH on women's health. Patients undergoing Cesarean sections following failure to progress in labor are at great risk for PPH and should theoretically benefit from an additional uterotonic agent. This study will be conducted to define whether the addition of ergonovine maleate to oxytocin, administered in a prophylactic way, reduces blood loss during Cesarean section for failure to progress in labor.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Treatments:
Ergonovine
Oxytocin
Criteria
Inclusion Criteria:

- Cesarean section secondary to failure to progress in labour

- First stage of labour

- Received oxytocin for at least 4 hours

Exclusion Criteria:

- Require General Anesthesia

- Cardiac Disease

- Hypertension

- Predisposition to uterine atony and postpartum hemorrhage