A Randomised Double Blind Placebo Controlled Trial-Local Anaesthesia and Pain Perception during Amniocentesis
Not Applicable
Completed
- Conditions
- Health Condition 1: O359- Maternal care for (suspected) fetal abnormality and damage, unspecified
- Registration Number
- CTRI/2020/10/028469
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 138
Inclusion Criteria
Singleton pregnancy and gestational age 15-24 weeks based on reliable last menstrual period and/or sonographic biometry in 1st trimester of pregnancy (11 to 13+6 weeks) having following indications-
h/o chromosomal abnormality in baby
high risk/intermediate risk cases according to aneuploidy results
Nuchal translucency >3.5 mm
Previous syndromic baby ,parents having balanced translocation,usg suggestive of any structural abnormality
Exclusion Criteria
patient having history of lignocaine allrgy
inability to rate pain score by visual analogue scale
patient refusal
abnormal sensory function based on history
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method