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Measuring different markers of labor pain in pregnant patients and its relatio

Not Applicable
Conditions
Health Condition 1: O82- Encounter for cesarean delivery without indication
Registration Number
CTRI/2023/07/055282
Lead Sponsor
AIIMS RESEARCH SECTION NEW DELHI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Singleton pregnancy

2. Term pregnancy

3. Elective and emergency cesarean section

Exclusion Criteria

1. Complicated pregnancy (e.g, Eclampsia, placental abruption, uterine abruption)

2. Contraindication to spinal anesthesia

3. H/o of Chronic Pain and neuropathic pain

4. H/o Substance use that has an effect on Central nervous system

5. Already receiving labor epidural

6. H/o Psychiatric illness

5. H/o of any neurological disease

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the CSF concentrations of noradrenaline, serotonin, GABA & glycine between pregnant women with labor pain & those without labor painTimepoint: After spinal anaesthesia
Secondary Outcome Measures
NameTimeMethod
To assess the correlation between each neurotransmitter & pain intensity in the Labour pain group <br/ ><br>To assess the blood level above neurotransmitter between pregnant women with labor pain & those without labor pain & its correlation with CSF value <br/ ><br>To evaluate the correlation among the four different neurotransmitters. <br/ ><br>Timepoint: After spinal anaesthesia
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