Skip to main content
MedPathMedPath Home
Clinical Trials/ISRCTN55359097
ISRCTN55359097
Completed
未知

A method comparison study comparing intra- and inter-user reproducibility of FeNO measurement using the NObreath® V2

Bedfont® Scientific Ltd0 sites186 target enrollmentSeptember 4, 2020
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Bedfont® Scientific Ltd
Enrollment
186
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 4, 2020
End Date
October 30, 2020
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Bedfont® Scientific Ltd

Eligibility Criteria

Inclusion Criteria

  • •1\. Aged 7 years or above
  • •2\. If on allergy immunotherapy treatment this must be a stable regimen during the study
  • •3\. Be capable of producing valid FeNO measurements via the NObreath®
  • •4\. Be capable of performing spirometry in accordance with ATS/ERS criteria

Exclusion Criteria

  • •1\. Hospitalisation related to asthma in the past 6 months
  • •2\. Use of oral corticosteroid in the 4 weeks prior to visit 1
  • •3\. Use of biological therapies e.g. mepolizumab in 12 weeks prior to visit 1
  • •4\. Other respiratory diseases e.g. COPD or cystic fibrosis
  • •5\. Known intolerance to inhaled corticosteroids or salbutamol
  • •6\. Cardiovascular conditions:
  • •6\.1\. Coronary artery disease
  • •6\.2\. High blood pressure
  • •6\.3\. Heart failure
  • •6\.4\. Diagnosed abnormality of heart rhythm

Outcomes

Primary Outcomes

Not specified

Similar Trials

Not yet recruiting
Phase 4
A clinical study to compare the the sedative drug combination dexmedetomidine plus ketamine and midazolam plus ketamine on patients undergoing short surgical procedures.Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecifiedHealth Condition 2: K929- Disease of digestive system, unspecifiedHealth Condition 3: N359- Urethral stricture, unspecified
CTRI/2021/08/035523Dr Seethal Ann Sunny
Completed
Not Applicable
A study to compare different intravenous fluids on certain blood parameters during the surgery in patients undergoing elective surgery for brain tumorsHealth Condition 1: O- Medical and Surgical
CTRI/2022/02/039979Dr Abinaya Prakashbabu 75
Not yet recruiting
Phase 4
Effects of adding fentanyl versus tramadol with hyperbaric bupivacaine for spinal anaesthesia in urological surgeries.
CTRI/2023/07/054882Dr Baig Mirza Wajeed
Recruiting
Not Applicable
Comparing the two different methods of the internal jugular central venous catheter in infants under one-month-oldDuring aspiration, puncture and other catheterization.During aspiration, puncture and other catheterizationY60.6
IRCT20210505051197N2Shahid Beheshti University of Medical Sciences64
Not yet recruiting
Not Applicable
TO COMPARE EFFICACY OF DEXMEDETOMIDINE AND NALBUPHINE FOR TREATMENT OF POSTSPINAL SHIVERINGHealth Condition 1: null- Patients posted for elective surgery under spinal anaesthesia who develop post spinal shivering
CTRI/2018/07/014854Dr Harpreet kaur