Comparative Study of intranasal Dexmedetomidine Versus oral Triclofos Sodium as premedicant in Children undergoing Computed Tomography Imaging : A Parallel Group Single Blind Randomised Controlled Trial.
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Two Groups will be compared in
研究概览
简要总结
SUMMARY: Name of candidate/Designation/Place of posting : Dr. Kabir Hossain , 1 st Year Post Graduate
Trainee, IPGME&R and SSKM Hospital, Kolkata.
Broad area and specific area- MD Anesthesiology, Session 2017-2020
Place of proposed research work and name of Institute/Department- Department of
Anesthesiology, IPGME&R and SSKM Hospital, Kolkata.
Name of proposed supervisor: Prof ( Dr ) Amita Pahari; Professor
, Department of Anesthesiology, IPGME&R and SSKM Hospital, Kolkata.
Name of proposed co-supervisor : Dr. Rajashree Biswas , Assistant Professor, Department of
Anesthesiology, IPGME&R and SSKM Hospital, Kolkata.
Proposed topic of research- Comparative Study of intranasal Dexmedetomidine Versus oral Triclofos Sodium as premedicant in Children undergoing Computed
Tomography Imaging : A Parallel Group Single Blind Randomised Controlled Trial.
Objective of proposed research- Time required to attain successful sedation level,recovery time from sedation,drug tolerance,haemodynamic changes,ease of child parent
separation,Radiologist and Anaesthesiologist satisfaction.
Background of present study– Good quality of CT immaging children needs sufficient immobility and anxiolysis. Various sedatives are used for this purpose and among them chloral hydrate derived triclofos sodium is one of the widely used sedative in children for immaging study.But it has a pungent odour with a bitter caustic taste and causes a high incidence of nausea and vomiting.Dexmedetomidine is a highly selective a2-adrenergic receptor agonist with sedative and mild analgesic effects and it has been increasingly used in paediatric non-invasive diagnostic procedures.It is easy to administer
intranasally and it does not require IV access and it is generally well tolerated.
Methodology- children aged between 1 to 6 years with ASA physical status 1 or 2 scheduled for CT immaging studies under sedation will be evaluated with history and physical examination before inclusion and will be admitted to radiological suite at least 1 h prior to imaging.. Oral drugs will be Aloe vera syrup as placebo and syrup Triclofos Sodium 100 mg/ml. Intranasl drug will be saline or dexmedetomidine 100 mcg/ml. EMLA cream will be applied at two preidentified venipuncture sites and sealed with occlusive dressing.For intranasal administration, the drug will be dripped into child’s nostrils using a tuberculin syringe. In my study before the CT immaging , children will drink 0.5 ml/kg. syrup and received 0.025 ml/kg nasal drop. Blood pressure, pulse rate and oxygen saturation, Respiratory Rate will be recorded before drug administration and then every 5 min,along with sedation (Modified Observer’s assessment of alertness / sedation scale). After achieving IV access, children will
be transferred to the CT table for imaging.
Expected outcome- Intranasal dexmedetomidine may yield better sedative effect and more acceptable,less failure rate;smooth recovery,minimal adverse effect to children undergoing CT imaging in comparison with
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Investigator Blinded
入排标准
- 年龄范围
- 1.00 Year(s) 至 6.00 Year(s)(—)
- 性别
- All
入选标准
- •Children between 1 to 6 years of age.
- •Children who are not well adapted for undergoing CT imaging .
排除标准
- •Known allergy or hypersensitivity reaction to Dexmedetomidine or Triclofos Sodium ;EMLA cream; and propofol.
- •Patients taking any other sedatives.
- •Patients with nasal infection & nasal pathology for intranasal route.
- •Patients with any significant cardiac or respiratory disease.
- •Patients with severe mental Retardation or gross neurodevelopmental disorder.
- •Patients with severe systemic diseases.
- •Refusal from parents to undergo study.
结局指标
主要结局
Two Groups will be compared in
时间窗: From 5 minutes prior to Drug administration to 1 hour after imaging study
terms of time required to attain
时间窗: From 5 minutes prior to Drug administration to 1 hour after imaging study
successful sedation level as per
时间窗: From 5 minutes prior to Drug administration to 1 hour after imaging study
MOAA/S scale between 0 and 3
时间窗: From 5 minutes prior to Drug administration to 1 hour after imaging study
次要结局
- Both the groups will be compared in terms(of)
