A scientific research to be conducted among women in labour to reduce labour pain using either of the two injections
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Antenatal women in labour with cervical dilatation 3cm
Term gestation
Spontaneous onset of labour
Singleton pregnancy with vertex presentation
Exclusion Criteria
Women with cephalopelvic disproportion
Previously scarred uterus (post myomectomy, post cesarean)
History of any drug allergy
Medical disorders complicating pregnancy like severe anemia, gestational diabetes mellitus, cardiac disease, pregnancy induced hypertension, pre-existing liver disorders, seizure disorders.
Non-reassuring NST
Intrauterine growth restriction (IUGR)
Intrauterine foetal death
Patients on antidepressants (e.g. SSRI)
Patients who are not willing to participate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method