Status:
WITHDRAWN
Dosing Strategies for Automated Mandatory Intermittent Boluses Technique for Epidural Labour Analgesia
Lead Sponsor:
Pravara Institute of Medical Sciences University
Conditions:
Primigravida in Labour Pains
Eligibility:
FEMALE
18-35 years
Phase:
NA
Brief Summary
The purpose of this study is to determine how manipulation of the programmed intermittent time interval and volume influences total drug use, quality of analgesia, and patient satisfaction during main...
Detailed Description
Research for the ideal technique of maintaining epidural analgesia after the initial-level block is ongoing. Continuous infusion techniques, use of more dilute solutions , PCEA , and different techniq...
Eligibility Criteria
Inclusion
- Full term women in spontaneous labor.
- Gestation greater than or equal to 37 weeks.
- Primigravida.
- Age group between 18 Years to 45 Years.
- ASA grade I or II
- Not having any complicated pregnancy
- Not having any systemic disorders.
Exclusion
- Not willing for Epidural analgesia.
- Unwilling to get enrolled in this study.
- Systemic disorder like diabetes mellitus, hypertension and heart disease, spine deformity, blood coagulation disorder, bad obstetric history and foetal abnormity.
- Multiple-pregnancy or abnormal presentation.
- Complicated pregnancy like pregnancy induced hypertension, placenta previa, abruptio placenta.
- Cervical dilatation less than 2 or greater than 5 at time of initiation of neuraxial analgesia.
- Chronic analgesic medications
- Systemic opioid labor analgesia prior to the initiation of neuraxial labor analgesia.
Key Trial Info
Start Date :
August 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01205360
Start Date
August 1 2010
End Date
October 1 2012
Last Update
September 21 2017
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