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临床试验/NCT05648656
NCT05648656招募中3 期

Efficacy of TXA Nebulization for the Treatment of Hemoptysis: A Randomized Controlled Clinical Trial

Post Graduate Institute of Medical Education and Research, Chandigarh1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年2月3日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
Quantity of hemoptysis

研究概览

简要总结

Hemoptysis is a common presentation in medical emergency. Prompt medical therapy, bronchoscopic and endovascular procedures remains the cornerstone of management for both diagnostic as well as therapeutic purpose in hemoptysis. Priority is given for medical management to achieve hemostasis and prevent aspiration as well as treatment of underlying etiology, before undertaking any definitive bronchoscopic or endovascular intervention. While majority of the patients are managed successfully by prompt medical therapy, only the refractory cases and life-threatening hemoptysis need more definitive procedures like DSA guided bronchial artery embolization and bronchoscopic procedures like endobronchial biocompatible glue, endobronchial embolization using silicone spigots, endobronchial stents, laser photocoagulation. Tranexamic acid is an anti-fibrinolytic agent which prevent breakdown of fibrin clots, thus helping in clot stabilization and controlling bleeding. As a medical therapy Tranexamic Acid is used for bleeding control in hemoptysis as well as other surgical or traumatic bleeding. Previously conducted institutional study comparing IV infusion of TXA to placebo in patients with sub massive hemoptysis showed results favoring TXA over placebo in terms of decreasing frequency & quantity of hemoptysis, duration of hospital stay and need for DSA/ broncoscopic/ surgical intervention and blood transfusion (1). While the oral and IV routes have been most commonly studied, use of novel approaches like aerosolized TXA and endobronchial instillation of TXA during bronchoscopy have showed positive results in achieving hemostasis in hemoptysis (2). A recently conducted RCT, to assess the effectiveness of TXA nebulization in sub-massive hemoptysis concluded that nebulized TXA is effective in reducing the frequency and quantity of hemoptysis. Nebulized TXA was also found to be safe as no severe ADR was noted during its use as per previous RCT as well as multiple case reports.

However, because of limited number of research with small sample size and barring some case reports evidence for the use of nebulized TXA is limited in hemoptysis. In hemoptysis nebulized form of TXA is supposed to reach local site of bleeding (lung/ airway) promptly at a higher concentration leading to rapid control of hemoptysis. So, this study has been planned to evaluate further this novel approach of TXA nebulization for the management of hemoptysis. Similarly, data regarding adverse drug reaction related to TXA nebulization is also limited. This study will produce additional information regarding efficacy, safety and ADR related to TXA nebulization.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All cases of active hemoptysis
  • irrespective of gender
  • age≥ 18 years

排除标准

  • Massive hemoptysis
  • Pregnancy
  • Drug allergy to TXA4
  • Renal failure
  • Receiving Oral Contraceptive Pills.
  • Already on blood thinner
  • Not willing for consent.

研究组 & 干预措施

TXA

Active Comparator

Nebulization with TXA 500mg/ 5mL 8 hourly for 2 days.

干预措施: TXA Nebulization (Drug)

Control

Placebo Comparator

Nebulization with 0.9%normal saline 5mL 8 hourly for 2 days

干预措施: 0.9% NS Nebulization (Other)

结局指标

主要结局

Quantity of hemoptysis

时间窗: 48 hours

Through collection of expectorated blood, quantityofhemoptysis per day will be compared at baseline and day2 (48hours) .

Visual analogue scale (VAS)

时间窗: 48 hours

Visual subjective assessment by the patient will be used to compare the amount of hemoptysis at baseline and day 2 (48 hours). VAS will be presented to the patients as a 100 mm line anchored by description with 'no-hemoptysis' at one end and 'worst imaginable hemoptysis' on the other end. Patients will be asked to mark a point on the 100 mm line to indicate the severity. A millimeter scale will be used to measure the score and this will provide 0-100 levels of hemoptysis and the score increases with increasing severity.

Frequency of hemoptysis

时间窗: 48 hours

Number of episode of hemoptysis per day will be compared at baseline and day 2 (48 hours)

次要结局

  • Resolution of hemoptysis(48 Hours)
  • Need for blood transfusion(48 Hours)
  • Need for intervention(48 Hours)
  • Adverse drug events(48 hours)
  • Duration of hospital stay(4 weeks)
  • Mortality(4 weeks)
  • Recurrence of hemoptysis(4 weeks)

研究者

发起方
Post Graduate Institute of Medical Education and Research, Chandigarh
申办方类型
Other
责任方
Principal Investigator
主要研究者

Deba Prasad Dhibar

Associate Professor

Post Graduate Institute of Medical Education and Research, Chandigarh

研究点 (1)

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