跳至主要内容
临床试验/CTRI/2025/06/088736
CTRI/2025/06/088736招募中2/3 期

A COMPARATIVE STUDY OF PREOXYGENATION WITH PRESSURE SUPORT VENTILATION , PRESSURESUPPORT VENTILATION WITH THE POSITIVE END-EXPIRATORY PRESSURE, AND SPONTANEOUS BREATHINGWITH FACE MASK DURING GENERAL ANAESTHESIA

MADHU MANOHAR V1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2025年6月20日最近更新:

试验速览

阶段
2/3 期
状态
招募中
发起方
入组人数
105
试验地点
1
主要终点
1. In all three groups time taken for desaturation till 92% of SpO2 (IN SECONDS)

研究概览

简要总结

  1. Among the pool of eligible candidates, after taking written informed consent

from study participants ,105 subjects will be selected randomly and will be

allotted into 3 groups, group I, group II and group III.( A simple randomisation

technique will be followed. A total of 105 random numbers will generated at the

beginning of the study and kept centrally with the study guide. While participants

will be kept blind to the procedure and group allocation, the same is not feasible

for the investigators due to the inherent nature of the interventions. Although the

statistician who performs the data analysis will be blind to the intervention, the

master chart and statistical review were also conducted by the study guide, who

will not blind to the intervention. )

  1. Once the subject is allocated to either of the three group, the subject will

continue to participate in the study.In the operating room, patients will be

positioned supine with their neck flexed and head extended. The American

Society of Anaesthesiologists (ASA) standard monitoring will be applied , and

pulse-oximetry of the same make will be used in all patients. Group allocation

will be disclosed to the intraoperative anesthesia team at this point.

  1. GA induction will be standardised. Fresh gas flow will be set at 10L/

min.Patient will be pre oxygenated for 3 minutes from this point by any of the

following methods in which they are allocated.

  1. Group I - The group with Facemask (with fresh gas flow of 10L/min and FiO2

100), patients will be breathing spontaneously with tidal volume breathing,

without bagging or pressure support .

  1. Group II - In the PSV group, the PSV will be given using BPL E-FLO 6C

Anesthesia Machine and circle absorbent system with face mask. Pressure

support of 10CmH2O and FIO2 100.6. Group III- In the PSV +PEEP group settings of PSV 10CMH2O, PEEP of 8

CmH2O, FIO2 100.

  1. After three minutes of pre oxygenation patient will be induced with propofol

(1.5-2.5 mg/Kg) bolus dose followed by propofol infusion of 200mcg/kg/min).

  1. Two check ventilation breath will be performed to ensure that the patient is

able to be ventilated - Vecuronium 0.1 mg/Kg will be administered and facemark

will be removed from patient.

  1. From this point ,time taken for desaturation till 92% of SpO2 (IN SECONDS)

will be recorded . Heamodynamic parameters (HR, NIBP) will be recorded. After

SpO2 reaches 92% , patients will be mask ventilated for 2 minutes, followed by

endotracheal intubation or supraglottic airway insertion will be performed and

anesthesia will be continued as per plan. .

  1. The correct placement of the ET tube will be confirmed by capnography and

five-point auscultation (five breaths). After this, standard management will be

followed for both ventilation and peri-operative management as per protocol for

all three groups.

11.Heamodynamic parameters will be recorded at the beginning of

preoxygeantion, at the end of pre oxygenation, at the end of safe apnea period

and 2 minutes after ventilation later.

12.The statistical analysis will be done by appropriate statistical methods like

mean,percentages, standard deviation, Chi-square test and other relevant type of

statistical tests depending upon the type of data collected.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • •Patients belonging to age group 18to 65 years undergoing elective operative procedure under general anesthesia.
  • •ASA grade 1 and grade 2
  • •Patients Room air peripheral oxygen saturation of more than 97%
  • •Body mass index (BMI) of 18 to 26.0 kg per metre square.

排除标准

  • •1.Patients with history of respiratory disease 2.Patients having lesions / tumours of tracheobronchial tree and upper airway.
  • •3.Patients with history of cardiac disorder affecting the effort tolerance 4.Patients with history of neurological disorder and neuromuscular disorders 5.Patients with anticipated difficult intubation.
  • •6.Patients posted for emergency surgeries 7.Pregnant patients and patients with risk of aspiration.

结局指标

主要结局

1. In all three groups time taken for desaturation till 92% of SpO2 (IN SECONDS)

时间窗: AT BASELINE

will be recorded .

时间窗: AT BASELINE

2. Heamodynamic parameters (HR, NIBP) will be recorded

时间窗: AT BASELINE

次要结局

  • Heamodynamic parameters (HR, NIBP) will be recorded(MEASUREMENT ET EVERY MIUTE TILL SPO2 REACHES 92% AND AFTER 2 MINUTES OF VENTILATION LATER)

研究者

发起方
MADHU MANOHAR V
申办方类型
Other [self]

研究点 (1)

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