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Comparison of two drugs paracetamol and tramadol in providing pain relief in labor pains

Phase 4
Not yet recruiting
Conditions
Encounter for full-term uncomplicated delivery,
Registration Number
CTRI/2020/06/025866
Lead Sponsor
Government Medical College and Hospital Chandigarh
Brief Summary

This study is a  prospective,randomized comparative study.It will compare the effect of paracetamol intravenous infusion with tramadol intravenous infusion in providing labor analgesia and maternal and fetal side effects.

Intravenous infusion of study drug will be started after assessing baseline Visual analogue score in active phase of labor in singelton pregnancy according to randomly divided two groups.

Paracetamol infusion in few studies done have shown to be safe and more efficacious than intravenous tramadol infusion  for  labor analgesia.It has no side effects of opioids like nausea, vomiting or sedation in the parturient and also safe for neonates.Paracetamol is also easily available, , affordable and easy to administer as tramadol.So, in this study we will compare the effect of  1g paracetamol and 1mg/Kg tramadol intravenous infusion  in providing labor analgesia.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
Female
Target Recruitment
72
Inclusion Criteria
  • 1.Patients for intented vaginal delivery in active phase of labor with cervical dilatation from 4-6cm 2.Gestational age (37-41 weeks) 3.Spontaneous or induced Labor 4.Age (18-35 years) 5.
  • Primigravida / Multigravida(upto parity 1) 6.Singlenton pregnancy with viable fetus 7.Vertex presentation 8.Patients not a candidate for neuraxial analgesia for various reasons(not willing/presence of contraindications,etc.) 9.Non scarred uterus.
Exclusion Criteria
  • 1.Medical disorder.
  • Pregestational Diabetes Mellitus, Rheumatic heart disease, chronic hypertension,Severe anaemia, Liver disease , Renal disease and Epilepsy 2.Preclampsia ,Eclampsia 3.Gestational diabetes mellitus on insulin therapy. 4.Use of any other kind of analgesia before recruitment in study. 5.Non reassuring fetal heart rate 6.Antepartum haemorrhage 7.Polyhydramnios,Intrauterine growth restriction 8.Chorioamnionitis 9.Hypersenstivity to paracetamol.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual analogue score assessment of labor analgesiaAt start of giving drug, at 1 hour and 3 hours of drug adminstration
Secondary Outcome Measures
NameTimeMethod
Duration of active phase of first stage of labor, duration of second stage of labor, fetal bradycardia, mode of delivery,respiratory depression in baby, neonatal apgar score,NICU admissionsFrom start of giving drug till the time of discharge from hospital

Trial Locations

Locations (1)

Labor room of Government Medical College and Hospital sector 32, Chandigarh

🇮🇳

Chandigarh, CHANDIGARH, India

Labor room of Government Medical College and Hospital sector 32, Chandigarh
🇮🇳Chandigarh, CHANDIGARH, India
Sania Jindal
Principal investigator
8847481411
saniajindal2708@gmail.com

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