CTRI/2018/08/015161
Not yet recruiting
Phase 4
Study of efficacy and safety of Intravenous Paracetamol Infusion as intrapartum analgesic: Randomized Control Trial
CRH Sikkim Manipal Institute of Medical Sciences0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- CRH Sikkim Manipal Institute of Medical Sciences
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Age between 18\-35 years.
- •2\.Primigravida and multigravida
- •3\.The gestational age between 37\- 42 weeks.
- •4\.Patient seeking analgesia.
- •5\.Single viable fetus.
- •6\.Vertex presentation.
- •7\.1st stage of labour with cervical dilatation 3\-4 cm (in active phase).
Exclusion Criteria
- •1\.Extreme of age (below 18\-above 35\).
- •2\.Multiple gestation.
- •3\.Malpresentation.
- •4\.Major degree of cephalopelvic disproportion.
- •5\.Any medical disorder with pregnancy e.g., Rheumatic heart disease, Diabetes mellitus, Hypertension.
- •6\.Use of any other kind of analgesia before recruitment in the study
- •7\.Scared uterus.
- •8\.Fetal distress.
- •9\.Antepartum hemorrhage.
- •10\.Polyhydramnios.
Outcomes
Primary Outcomes
Not specified
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