None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Term Pregnant women reporting to the department of Obstetrics & Gynaecology who will be undergoing caesarean section and giving informed consent in the Regional Institute of Medical Sciences, a tertiary care centre of Imphal, Manipur
Exclusion criteria
Exclusion criteria: Presence of Hypertension, antepartum haemorrhage, fibroid uterus or history of myomectomy, cardiac, renal or liver diseases, epilepsy, bleeding disorders, general anaesthesia and history of hypersensitivity to any drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the amount of blood loss as well as the uterine tone following carbetocin and oxytocin in caesareansectionTimepoint: Blood loss, Uterine tone and Vitals are monitored immediately, 2 hours and 24 hours after delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the efficacy of the drugs in terms of additional interventions needed and drop in haemoglobinTimepoint: On admission and 24 hours after delivery | — |
Countries
India
Contacts
Regional Institute of Medical Sciences