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Indomethacin for Refractory Chronic Cough

Primary Purpose

Refractory Chronic Cough

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
indomethacin
Placebo
Omeprazole
Sponsored by
The First Affiliated Hospital of Guangzhou Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Chronic Cough

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

1)18 years old ≤ age ≤ 60 years old, male or female; 2)Chronic cough lasting more than 8 weeks as the sole or predominant symptom, without abnormalities on chest radiograph; 3)Chronic cough remains after investigation and supervised therapeutic trial(s) conducted according to "Clinical Practice Guidelines for Diagnosis and Management of Cough (2015)" 4)Cough VAS (0-100mm) ≥ 30 mm

Exclusion Criteria:

  1. Patients had any contraindications to indomethacin;
  2. Patients had active respiratory disease (such as chronic obstructive pulmonary Disease or untreated asthma), or moderate or above obstructive or restrictive or mixed pulmonary ventilation dysfunction;
  3. Patients had a respiratory tract infection in the month before randomization;
  4. Patients were taking an angiotensin-converting enzyme inhibitor;
  5. Patient were pregnant or breastfeeding, or had impaired kidney function;
  6. Current and recent smokers (<6 months' abstinence), or ex-smokers with more than 20 pack-years (20 cigarettes per pack).

Sites / Locations

  • The First Affiliated Hospital Of Guangzhou Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

indomethacin treatment group

placebo treatment group

Arm Description

indomethacin (75mg, bid) + omeprazole (20mg, qd)

placebo (75mg, bid) + omeprazole (20mg, qd)

Outcomes

Primary Outcome Measures

Change from Baseline Cough Severity
Outcome measure: Cough visual analogue scales (Cough VAS). Score range: 0-100mm (0 mean no cough, 100 represent that cough is the most severe in his/her life. Scoring higher on cough VAS mean more severe cough he/she has. )
Change of cough-specific-quality-of-life
Outcome measure: Leicester Cough Questionnaire (LCQ). Score range: 3-21 (Higher values represent a better outcome.)

Secondary Outcome Measures

frequency of patients'coughs
Outcome measure: cough count in one hour
laryngeal dysfunction score
Outcome measure: Laryngeal dysfunction questionnaire (Higher score represent a better outcome)
cough reflex sensitivity
Outcome measure: LogC5 of Capsaicin cough challenge

Full Information

First Posted
August 31, 2018
Last Updated
November 22, 2018
Sponsor
The First Affiliated Hospital of Guangzhou Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03662269
Brief Title
Indomethacin for Refractory Chronic Cough
Official Title
Indomethacin for Refractory Chronic Cough: a Randomized, Double-blind, Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Unknown status
Study Start Date
October 22, 2018 (Actual)
Primary Completion Date
August 15, 2020 (Anticipated)
Study Completion Date
December 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital of Guangzhou Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic cough is a common complain of patients in respiratory clinic and its global prevalence was up to 9.6%. Persistent cough of unexplained origin is a significant health issue that occurs in up to 5% to 10% of patients seeking medical assistance for a chronic cough and from 0% to 46% of patients referred to specialty cough clinics. Previous studies showed that sputum prostaglandin D2( PGD2) and prostaglandin E2 (PGE2) concentrations were significantly higher in chronic cough. And some research showed that Inhaled PGE2 /PGF2α /PGD2 / PGI2/ 6-oxo-PGF1a could induced cough. And PGE2 /PGF2α/PGI2/thromboxane A2 (TXA2) also increased the sensitivity of the cough reflex. All these five primary prostaglandins were synthesized though the metabolism of arachidonic acid via the cyclooxygenase pathway. Indomethacin is a strong inhibitor of cyclooxygenase , which decrease the level of prostaglandins in airway. The investigator's preliminary study showed that indomethacin could relieve cough and improve cough sensitivity of some patients with refractory cough. Therefore this randomized, double-blind, placebo-controlled trial were designed to investigate whether indomethacin can relive cough in patients with refractory cough and to explore the possible mechanism of indomethacin in improving cough in patients with refractory cough.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Chronic Cough

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
a randomized, double-blind, placebo-controlled trial
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
indomethacin treatment group
Arm Type
Experimental
Arm Description
indomethacin (75mg, bid) + omeprazole (20mg, qd)
Arm Title
placebo treatment group
Arm Type
Placebo Comparator
Arm Description
placebo (75mg, bid) + omeprazole (20mg, qd)
Intervention Type
Drug
Intervention Name(s)
indomethacin
Other Intervention Name(s)
Indometacin sustained-release capsules
Intervention Description
indomethacin (75mg, bid, po, 14days)
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo (75mg, bid, po, 14days)
Intervention Type
Drug
Intervention Name(s)
Omeprazole
Intervention Description
placebo (20mg, qd, po, 14days)
Primary Outcome Measure Information:
Title
Change from Baseline Cough Severity
Description
Outcome measure: Cough visual analogue scales (Cough VAS). Score range: 0-100mm (0 mean no cough, 100 represent that cough is the most severe in his/her life. Scoring higher on cough VAS mean more severe cough he/she has. )
Time Frame
1, 3, 7, 10, 14, 21day
Title
Change of cough-specific-quality-of-life
Description
Outcome measure: Leicester Cough Questionnaire (LCQ). Score range: 3-21 (Higher values represent a better outcome.)
Time Frame
1, 14, 21 day
Secondary Outcome Measure Information:
Title
frequency of patients'coughs
Description
Outcome measure: cough count in one hour
Time Frame
1, 7, 14 day
Title
laryngeal dysfunction score
Description
Outcome measure: Laryngeal dysfunction questionnaire (Higher score represent a better outcome)
Time Frame
1, 7, 14 day
Title
cough reflex sensitivity
Description
Outcome measure: LogC5 of Capsaicin cough challenge
Time Frame
1, 7, 14, 21 day
Other Pre-specified Outcome Measures:
Title
change of airway arachidonic acid metabolism
Description
Concentration of PGE2, PGF2α, PGD2, 6-Keto-PGF1α, TXB2, leukotriene B4(LTB4) and cys-LTs in induced sputum
Time Frame
1, 7, 14, 21 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1)18 years old ≤ age ≤ 60 years old, male or female; 2)Chronic cough lasting more than 8 weeks as the sole or predominant symptom, without abnormalities on chest radiograph; 3)Chronic cough remains after investigation and supervised therapeutic trial(s) conducted according to "Clinical Practice Guidelines for Diagnosis and Management of Cough (2015)" 4)Cough VAS (0-100mm) ≥ 30 mm Exclusion Criteria: Patients had any contraindications to indomethacin; Patients had active respiratory disease (such as chronic obstructive pulmonary Disease or untreated asthma), or moderate or above obstructive or restrictive or mixed pulmonary ventilation dysfunction; Patients had a respiratory tract infection in the month before randomization; Patients were taking an angiotensin-converting enzyme inhibitor; Patient were pregnant or breastfeeding, or had impaired kidney function; Current and recent smokers (<6 months' abstinence), or ex-smokers with more than 20 pack-years (20 cigarettes per pack).
Facility Information:
Facility Name
The First Affiliated Hospital Of Guangzhou Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
520120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kefang Lai, PHD
Phone
83062893
Ext
020
Email
klai@163.com
First Name & Middle Initial & Last Name & Degree
Kefang Lai, PHD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Study Protocol Statistical Analysis Plan (SAP)

Learn more about this trial

Indomethacin for Refractory Chronic Cough

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