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临床试验/CTRI/2025/12/099658
CTRI/2025/12/099658尚未招募不适用

Comparative study of Neonatal Pain During Heel Prick Using an Automatic Lancet Versus 26-Gauge Needle:A Randomized Controlled Trial

AISWARYA S KOTTOOR1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2025年12月22日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
126
试验地点
1

研究概览

简要总结

The title of my study is Comparative study of Neonatal Pain During Heel Prick Using an Automatic Lancet Versus 26 Gauge Needle A Randomized Controlled Trial

Aim of the study is to compare the intensity of pain experienced by neonates during heel prick  performed using an automatic lancet versus a 26 gauge needle using a validated pain scale  NIPS SCORE in order to determine the more effective method for minimizing procedural pain in newborns

Primary objective is to compare the pain response in neonates during heel prick using an automatic lancet versus a 26G Needle

Secondary objectives include assessment of physiological factors such as heart rate oxygen saturation before during and after the procedure   evaluate the incidence of local complications like bruising bleeding duration skin trauma associated with each method and   access procedural efficiency

Sampling technique is STRATIFIED RANDOMIZATION

Sample size is 126 Methodology is after applying inclusion and exclusion criteria First stratification done on the basis of gestational age TERM or PRETERM

BY SNOSE method allocating neonates into groups

Group 1 Heel prick using Automatic lancet

Group 2 Heel prick using 26G needle

Automatic lancet will be set at a depth of 1mm for term and 0.85mm for preterm neonates

Choose the medial or lateral plantar surface of heel avoiding central area to prevent injury to calcaneus

Clean the selected area with spirit cotton and allow area to dry

Perform the heel prick by holding the needle or lancet at 90 degrees

5 minutes video recording of the procedure will be taken without showing the instrument used

Video will be analysed by thesis guide and pain in neonates will be scored using NIPS scoring system

Secondary objectives like procedure time analysis tissue injury physiological parameters like SpO2 and Heart rate is measured simultaneously

Video captured such that the person assessing NIPS score is not able to see the instrument used for heel prick thereby assuring blinding

Video anonymity cannot be implemented as facial expression is essential for NIPS scoring

Data protected by ensuring access to videos only by the primary investigator and  score accessor

Data will be digitized using Excel and analysed using SPSS v25

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
0.00 Day(s) 至 7.00 Day(s)(—)
性别
All

入选标准

  • ALL NEONATES BORN IN VINAYAKA MISSIONS MEDICAL COLLEGE AND HOSPITAL REQUIRING SUGAR MONITORING LIKE INFANT OF DIABETIC MOTHER SMALL FOR GESTATIONAL AGE BABIES LOW BIRTH WEIGHT BABIES BABIES WHOSE MOTHERS ARE HAVING POOR SECRETION.

排除标准

  • BABIES WITH VERY LOW BIRTH WEIGHT ON MECHANICAL VENTILATION CONGENITAL ANOMALIES SEVERE MEDICAL OR SURGICAL CONDITIONS PRIOR PRICKS IN PAST 24 HOURS PARENTAL REFUSAL.

研究者

发起方
AISWARYA S KOTTOOR
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

AISWARYA S KOTTOOR

VINAYAKA MISSIONS MEDICAL COLLEGE AND HOSPITAL KARAIKAL

研究点 (1)

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