CTRI/2018/05/014020Active, not recruiting未知
Comparison of intravenous Paracetamol versus intravenous Tramadol for analgesia in labour
BPS Government medical college0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Active, not recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Primigravid and multigravid women of age ranges from 18 to 35 years with low risk to both mother and fetus (single live fetus in cephalic presentation without any associated obstetric and medical complication)
- •2. Women with gestational age ranges from 37 to 42 weeks
- •3. Women in active stage of labour (with cervical dilatation of 3-5 cm and with moderate intensity uterine contractions of 2-3 per 10 minutes each lasting for 30-45 seconds with good inter relaxation period in between), whether spontaneous or induced labour
- •4. Women with reactive Non Stress Test (NST) before recruitment into study
- •5. Women seeking labour analgesia
Exclusion Criteria
- •1. Women with high risk pregnancy like severe Intrauterine growth retardation (IUGR), multiple gestation, malpresentation, polyhydroamnios, oligohydroamnios, pre-mature rupture of membranes
- •2. Women with any medical disorder with pregnancy like severe anaemia, hypertensive disorders, diabetes mellitus, hypothyroidism
- •3. Women with scarred uterus
- •4. Women with obstetric indication for Lower Segment Caesarean Section before recruitment to study
- •5. Women in advanced stage of labour if cervical dilatation more than 5 cm
- •6. Women with use of any other kind of analgesia before recruitment to study
- •7. Women with previous history of hypersensitivity to Tramadol or Paracetamol
- •8. Women with deranged liver function test
- •9. Women not willing to participate in study
Investigators
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