Title

Study of Interventional Pulmonologic Treatment of Benign Central Airway Fibrotic Stricture
Prospective, Randomized, Open, Controlled, Multicenter Stucy of Interventional Pulmonologic Treatment of Benign Central Airway Fibrotic Stricture
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Unknown status
  • Intervention/Treatment

    mitomycin ...
  • Study Participants

    160
The purpose of this study is to evaluate the efficacy and safety of four interventional pulmonology techniques for the treatment of fibrotic central airway stricture.

The four techniques are:

balloon dilation
balloon dilation plus cryotherapy
balloon dilation plus spiculiform electrosurgery
balloon dilation plus mitomycin C injection
Study Started
Dec 31
2014
Primary Completion
Dec 31
2017
Anticipated
Study Completion
Dec 31
2017
Anticipated
Last Update
Nov 10
2014
Estimate

Device balloon dilation

Procedure cryotherapy

Procedure spiculiform electrosurgery

Drug mitomycin C

balloon dilation Experimental

give the cases balloon dilation as the intervention

balloon dilation plus cryotherapy Experimental

give the cases balloon dilation plus cryotherapy as the intervention

BD plus spiculiform electrosurgery Experimental

give the cases balloon dilation plus spiculiform electrosurgery as the intervention

BD plus mitomycin C Experimental

give the cases Balloon dilation plus mitomycin C as the intervention

Criteria

Inclusion Criteria:

tracheal incision,intubation or bronchial tuberculosis caused central airway fibrotic stenosis
the degree of stenosis is above 50%
estimated survival duration is longer than 3 months
recieved no treatment one month before
can understand the statement informed consent
agree to enroll in the study

Exclusion Criteria:

older than 70 years or younger than 18 years
not fibrotic stenosis
not central airway stenosis
existence of lumina collapse or twisting
severe arrhythmia, myocardial ischemia or hypertensive crisis
coagulation disorders
existence of severe organ disfunction
allergic to anesthesia drugs
refuse to participate the study
No Results Posted