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CTRI Number  CTRI/2024/02/062197 [Registered on: 01/02/2024] Trial Registered Prospectively
Last Modified On: 31/01/2024
Post Graduate Thesis  No 
Type of Trial  Observational 
Type of Study   Follow Up Study 
Study Design  Other 
Public Title of Study   To study the outcomes of treatments prescribed by pulmonologists for post TB COPD patients 
Scientific Title of Study   Treatment outcome among Post TB COPD labelled patients: A prospective cohort study 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
ARISE/Post TB COPD/05/2023  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sundeep Salvi 
Designation  Director 
Affiliation  Pulmocare Research and Education Foundation 
Address  Sakore Nagar, Faith Centre. Viman nagar. Pune

Pune
MAHARASHTRA
411060
India 
Phone  9921211000  
Fax    
Email  sundeepsalvi@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Sundeep Salvi 
Designation  Director 
Affiliation  Pulmocare Research and Education Foundation 
Address  Sakore Nagar, Faith Centre. Viman nagar. Pune

Pune
MAHARASHTRA
411060
India 
Phone  9921211000  
Fax    
Email  sundeepsalvi@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Sundeep Salvi 
Designation  Director 
Affiliation  Pulmocare Research and Education Foundation 
Address  Sakore Nagar, Faith Centre. Viman nagar. Pune


MAHARASHTRA
411060
India 
Phone  9921211000  
Fax    
Email  sundeepsalvi@gmail.com  
 
Source of Monetary or Material Support  
Cipla Pvt Ltd 
 
Primary Sponsor  
Name  Cipla Pvt Ltd 
Address  Cipla House, Peninsula Business Park, Ganpatrao Kadam Marg, Lower Parel, Mumbai-400013 
Type of Sponsor  Pharmaceutical industry-Indian 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 20  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Mahendra Kumar Gupta  AANCH Hospital  K-32, SL Marg, near kesar restaurant, VG Nagar, Malviya Nagar, Income Tax Colony, Durgapura, Jaipur, Rajasthan 302018
Jaipur
RAJASTHAN 
9950808583

hospital211@gmail.com 
Dr Venkata Kasiram  Aditya Multispecaility hospital  13-4-64, 4th Ln, GunturvariThota, Kothapeta, Guntur, Andhra Pradesh 522001
Guntur
ANDHRA PRADESH 
9966083232

kasiram1488@gmail.com 
Dr Anikl Kumar Singh  Chandan Hospital  VIJAYANT KHAND, GOMTI NAGAR, LUCKNOW
Lucknow
UTTAR PRADESH 
9650170666

draksinghchestspecialist@gmail.com 
Dr Alimuddin N M  Chest Care Clinic  C/O Chest Care Clinic, 20-6-530, Shah Ali Banda, Shah Ali Banda, Hyderabad - 500065
Hyderabad
TELANGANA 
9949671249

aleem95@yahoo.com 
Dr Jaymohan Unnithan  Hindustan Hospital  522/3, Hindustan Hospital Rd, behind EB Substation, Peelamedu, Coimbatore, Tamil Nadu 641028
Coimbatore
TAMIL NADU 
9443712821

unnithan2@gmail.com 
Dr Nanda Gopal   Hindustan Hospital  522/3, Hindustan Hospital Rd, behind EB Substation, Peelamedu, Coimbatore, Tamil Nadu 641028
Coimbatore
TAMIL NADU 
9842780383

dr_nanda@yahoo.com 
Dr S Nagarajan  Hindustan Hospital  522/3, Hindustan Hospital Rd, behind EB Substation, Peelamedu, Coimbatore, Tamil Nadu 641028
Coimbatore
TAMIL NADU 
9842780383

nagrajsri@gmail.com 
Dr Shrikanth Krishnamurthy   Hindustan Hospital  522/3, Hindustan Hospital Rd, behind EB Substation, Peelamedu, Coimbatore, Tamil Nadu 641028
Coimbatore
TAMIL NADU 
9894257706

drsrikanthcbe@gmail.com 
Dr Parthasarathy Bhattacharya  Institute of Pulmocare and Research  Street Number 0327, DG 8, Action Area I, Newtown, Chakpachuria, West Bengal 700156
Kolkata
WEST BENGAL 
9831003144

parthachest@yahoo.com 
Dr Souvik Sarkar  Jawaharlal Nehru Medical College and AVBR Hospitals  Jawaharlal Nehru Medical College and AVBR Hospitals, Sawangi Meghe Wardha
Wardha
MAHARASHTRA 
8051207123

docsouviksarkar@gmail.com 
Dr Sonia Dalal  Kalyan Hospital  101 - 102,Shree Hari Corner,R.C Dutt Road., behind Express Hotel, Vadodara, Gujarat 390015
Vadodara
GUJARAT 
9898089310

drsoniadalal@hotmail.com 
Dr Arjun Padmanabhan  KIMS Health   KIMSHEALTH, P.B.No.1, Anayara P.O, Trivandrum – 695029, Kerala, India
Thiruvananthapuram
KERALA 
9447151919

dr.p.arjun@gmail.com 
Dr Abhinav Chaudhary  Lungs Heal Clinic  7/10/158, Hans Puram Colony, Deokali, Faizabad.
Faizabad
UTTAR PRADESH 
8090242558

abhinavmlb@gmail.com 
Dr Suhas Bardapurkar  Shree Nursing Home  V8HG+H48, Aurangpura - Samarthnagar Rd, Gulmandi, Shahgunj, Aurangabad, Maharashtra 431001
Aurangabad
MAHARASHTRA 
9423150213

drsuhasbardapurkar@gmail.com 
Dr Narendra Maddur  SUNRISE HOPITAL   SUNRISE HOPITAL , BESIDE NEW BUSTAND , SIDDIPET, TELANGANA 502013
Hyderabad
TELANGANA 
9989948998

narenmaddur@gmail.com 
Dr Vivek Vardhan  Swasa Hospital  beside Narayanguda Flyover, next to Taj Mahal Hotel, Narayanguda, Hyderabad, Telangana 500029
Hyderabad
TELANGANA 
9502077555

swasahospital123@gmail.com 
Dr Kalpesh Panchal  Swastik Lungs care and Allergy clinic  301, Shlok Infinity Opp. Vishwakarma Temple Nr. Gota, Railway, Dindayal Upadhyay Overbridge, Chandlodiya, Ahmedabad, Gujarat 382481
Ahmadabad
GUJARAT 
9712199914

kalpesh2434@gmail.com 
Dr Vaibhav Kubal  The Diagnostic Hub  Florence, Nehru Rd, next to Axis Bank, Vakola, Santacruz East, Mumbai, Maharashtra 400055
Mumbai
MAHARASHTRA 
9769066635

drvaibhavkubal@gmail.com 
Dr Bharat Toshniwal  Toshniwal Chest Hopsital  Ghamodiya Factory Area, Vazirabad Main Road, Maharashtra 431601
Nanded
MAHARASHTRA 
9860192121

bharattosh@gmail.com 
Dr Nagarjuna Matru  Yashodha Hospital  Yashodha Hospital, Raj Bhavan Rd, Somajiguda, Hyderabad, Telangana 500082
Hyderabad
TELANGANA 
9100935638

pulmoyhsmj@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 3  
Name of Committee  Approval Status 
Institutional Human Ethics comittee  Submittted/Under Review 
Royal Pune Independent Ethics Comittee  Approved 
Royal Pune Independent Ethics Comittee  Submittted/Under Review 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: J988||Other specified respiratory disorders,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  NIL  NIL 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  95.00 Year(s)
Gender  Both 
Details  1.Male and female participants ≥18 years of age
2.Diagnosed cases of Post TB COPD (cured from TB)
3.Spirometry FEV1/FVC < 70% (post BD)
4.Symptomatic – Any respiratory symptoms 
 
ExclusionCriteria 
Details  1. Participants below the age of 18 years
2. Participants unable to perform spirometry or/and lung oscillometry.
3. Participants not willing to provide consent to participate.
4. Relapse cases of TB
5. TB patients who are on Koch’s treatment
6. Cases of Asthma or all those who have not developed COPD post TB recovery 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
1.Change in symptoms.
2.Quality of life
3.Exacerbations-need for hospital visit or hospitalizations
4.Spirometry and oscillometry parameters 
Baseline, 1 month and 3 months 
 
Secondary Outcome  
Outcome  TimePoints 
NIL  NIL 
 
Target Sample Size   Total Sample Size="200"
Sample Size from India="200" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   16/02/2024 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  
Study Synopsis
A. Title: Treatment outcome among Post TB COPD labelled patients: A prospective cohort study
B. Background
Approximately 10 million cases of Pulmonary TB are diagnosed every year of which 85% are cured (1). In 2020 there were an estimated 155 million TB survivors and India is likely to have 36-400 million TB survivors. Evidence suggests that a significant proportion of TB treated patients develop post TB lung disease i.e., Chronic Obstructive Pulmonary Disease (COPD). A study called the Post TB spirometry study conducted through the Respiratory Research Network (RRN), in Pune across 27 centers in India, identified 54% of COPD patients amongst the TB treated cohort in the past. Interestingly, of the total cohort 26% were identified as PRISm (Preserved Ratio Impaired Spirometry), which will eventually develop into COPD in the future (to be published).
Even with the increasing burden of Post TB COPD, an appropriate pharmacotherapy is still not known. Through this prospective observational study, various pharmacotherapy will be explored and the most appropriate treatment will be identified by studying the effect of various treatment options on outcomes such as improvement in symptoms, quality of life, decreased number of exacerbations, need for rescue medication, improvement in spirometry and lung oscillometry values.
C. Research Question: What are the treatment outcomes among Post TB COPD .
D. Aim of the Study:
•To study the treatment outcomes among Post TB COPD labelled patients.
E. Study Design: Real world, observational, longitudinal follow-up study
F.Sample Size: 200 Post TB COPD patients
G.Study Population:
Patients of post TB COPD: Adult (>18 years) Male and female subjects previously diagnosed with Pulmonary TB (diagnosis based on Sputum Exam, Chest Xray, HRCT (if available) or other immunological tests) and who have taken full treatment, diagnosed as treatment cure by the treating physician, advised to stop anti-TB treatment. These patients continue to have respiratory symptoms (cough, shortness of breath, sputum) and spirometry shows presence of fixed airflow obstruction (Post-bronchodilator FEV1/FVC < 70%) (these patients will include smokers and non-smokers, drug resistant TB, not drug resistant and then do a sub-group analysis).

Inclusion Criteria
1.Male and female participants ≥18 years of age
2.Diagnosed cases of Post TB COPD (cured from TB)
3.Spirometry FEV1/FVC < 70% (post BD)
4.Patients with respiratory symptoms
Exclusion criteria
1.Participants below the age of 18 years
2.Participants unable to perform spirometry or/and lung oscillometry.
3.Participants not willing to provide consent to participate.
4.Relapse case of TB (Physician defined)
5.TB patients who are on Koch’s treatment
6.Cases of Asthma or all those who have not developed COPD post TB recovery
H.Study Design:
Patients fulfilling the criteria of Post TB COPD will be included into the study. The treating physician will decide what pharmacotherapy needs to be given.
Post TB COPD treatment:
1.No Treatment
2.Inhalation treatment (potential prescriptions that could be prescribed)
•SABA
•SABA+SAMA
•LAMA
•LABA+LAMA
•ICS+LABA
•ICS+LABA+LAMA
3.Other treatment
Baseline values (symptoms, quality of life, exacerbations, need for rescue medication, spirometry, lung oscillometry if available) and follow up changes will be noted during the follow up visits (preferably 1 month and 3 months after starting the treatment). All relevant information will be collected during the study period.

End points: Change in symptoms, quality of life, exacerbations, need for hospital visit or hospitalizations, spirometry and oscillometry parameters will be captured (preferably 1 month and 3 months after starting the treatment)

J.Statistical analysis plan
The primary objective of this study is to report the efficacy and safety of different pharmacotherapies prescribed in patients with Post TB COPD. Descriptive statistics which mainly includes frequency and percentages for all categorical variables, and mean and standard deviation for continuous variables. Differences between baseline values and different time points will be captured using paired t tests. Comparisons between different treatment regiments will be described descriptively.
 
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