跳至主要内容
临床试验/CTRI/2019/03/018061
CTRI/2019/03/018061尚未招募Unknown

A Comparative Evaluation of a Novel Technique for Bronchoscopy Guided Tracheobronchial Foreign BodyRemoval in Children-A Randomised Controlled Trial

Richa Rai1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2019年1月4日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
1.To compare the effect on intra-procedure and post-procedure hemodynamics

研究概览

简要总结

30 patients will be randomly divided into 2 groups. Patients will be premedicated with 0.05 mg/kg and glycopyrrolate 10 mcg/kg.Induction will be done in both groups with fentanyl 2 mcg/kg and propofol 1-2 mg/kg in titrated dose before the start of procedure. 

Group A - Patients will be nebulized with 2ml of 2% lignocaine for 10-15 minutes in preoperative room before induction. After induction, transtracheal block will be done with 1 ml of 2% plain lignocaine 10 minutes prior to procedure.

Group B - Nebulisation and airway block will done with normal saline for blinding purpose.

Immediately followed by infusion of propofol @50-150 mcg/kg/min for maintenance anesthesia. We will use rescue propofol intermittently depending upon the patients’ requirements. Rigid bronchoscopy will be performed by pediatric surgeons in all cases . HR, SPO2 and NIBP will be recorded   continuously every 3 minutes throughout the procedure and patient will be observed for any event of desaturation or other adverse effects. All patients will be maintained on the spontaneous ventilation. After completion of procedure and stopping anesthetics, we will note the time duration of return to full consciousness and baseline saturation with any eventful episodes. To monitor recovery of consciousness at the end of procedure , MOAA(Modified Observers Assessment of Alertness/Sedation) scale will be used .

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

年龄范围
2.00 Year(s) 至 5.00 Year(s)(—)
性别
All

入选标准

  • 1.ASA grade I to II 2.Recent H/O of tracheobronchial foreign body aspiration 3.Parents giving consent for participation in the study.

排除标准

  • 1.Bronchoscopy through tracheostomy 2.Anterior neck swelling 3.Known allergy to local anesthetics 4.Renal, hepatic, or cardiovascular dysfunction, neurological disorders 5.Mental retardation or delayed milestones 6.Suspected coagulopathy 7.Parents refusal to participate in the study.

结局指标

主要结局

1.To compare the effect on intra-procedure and post-procedure hemodynamics

时间窗: Heart rate,Non-invasive blood pressure and saturation will be recorded continuously every 3 minutes throughout the procedure and till return of consciousness.

(Heart Rate, Non-Invasive Blood Pressure) and oxygen saturation.

时间窗: Heart rate,Non-invasive blood pressure and saturation will be recorded continuously every 3 minutes throughout the procedure and till return of consciousness.

2.Total dose of propofol used during procedure in both the groups.

时间窗: Heart rate,Non-invasive blood pressure and saturation will be recorded continuously every 3 minutes throughout the procedure and till return of consciousness.

3.Post-procedure recovery

时间窗: Heart rate,Non-invasive blood pressure and saturation will be recorded continuously every 3 minutes throughout the procedure and till return of consciousness.

次要结局

  • To look for complications encountered in such procedures like airway intervention, bronchospasm, laryngospasm, vocal cord injury and laryngeal or subglottic odema in both groups.(Complications noted from start of bronchoscopy till completion of procedure and return of consciousness every 5 minutes)

研究者

发起方
Richa Rai
申办方类型
Other [self]

研究点 (1)

Loading locations...

相似试验