Comparison of labour outcomes with and without use of test dose for labour analgesia
Phase 3
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2022/01/039117
- Lead Sponsor
- Amrita Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All consenting parturient of American society of anaesthesiologists, grade 2 having uncomplicated cephalic singleton pregnancy between age group of 18 t0 40 years and desirous of having a labour epidural
Exclusion Criteria
Patients with hypersensitivity to study drugs, bleeding disorders, decreased platelet counts, sepsis, spinal column deformities and history of spine surgery will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective of our study is to compare the incidence of numbness associated with labour epidural with and without a test dose.Timepoint: upto delivery
- Secondary Outcome Measures
Name Time Method The secondary objectives include comparison of onset of analgesia, duration of analgesia with the first bolus dose, hemodynamics, mode of delivery and fetal outcome (assessed by umbilical vein ABG and Apgar score).Timepoint: upto delivery