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Pulmonary Tuberculosis Patients With Diabetes Mellitus (TANDEM)

Primary Purpose

Diabetes Mellitus, Pulmonary Tuberculosis

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
intensive monitoring
Sponsored by
Universitas Padjadjaran
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus focused on measuring diabetes mellitus, tuberculosis, management, randomized controlled trial

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • adult (> 18 years old) diabetes mellitus patients
  • diagnosed as having active pulmonary TB
  • willing to join the study

Exclusion Criteria:

  • under TB treatment more than 72 hours
  • steroid-induced or gestational diabetes

Sites / Locations

  • Faculty of Medicine, Universitas Padjadjaran
  • Universidad Peruana Cayetano Heredia
  • University of Medicine and Pharmacy Craiova

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

intensive monitoring

standard monitoring

Arm Description

more intensive monitoring strategy of blood glucose and clinical review

glucose monitoring followed the prevailing practice at each site

Outcomes

Primary Outcome Measures

Better diabetes control in diabetes patients with tuberculosis under treatment
Diabetes control is determined by HbA1c level (unit: %) which will be measured at month 3 and 6 of TB treatment.

Secondary Outcome Measures

Cost-effectiveness of different strategies for diabetes management during TB treatment
Cost analysis will include all cost for lab analysis, transportation for follow up visit, expenses for medications, all complications caused by uncontrolled diabetes (including hospitalization, medications for co morbidities)
Measurement of long-term requirements for diabetes management in TB patients diagnosed with diabetes after TB treatment completed
Clinical characteristics (i.e. blood pressure, glucose control, kidney function, quality of life (QoL) of diabetes mellitus patients with TB after completing TB treatment will be measured and will be compared between both groups.
Association between glycemic control and clinical-microbiological response to TB treatment
Association between glycemic control and clinical response to TB treatment will be determined by measuring: increasing of body weight, symptoms relieve, treatment outcome (cured, completed, failure and default), and will be compared between groups. Association between glycemic control and microbiological response to TB treatment will be determined by measuring sputum conversion time (time to negative culture), and will be compared between groups.

Full Information

First Posted
March 19, 2014
Last Updated
April 17, 2019
Sponsor
Universitas Padjadjaran
Collaborators
London School of Hygiene and Tropical Medicine, Radboud University Medical Center, Leiden University Medical Center, University of Stellenbosch, St George's, University of London, University of Otago, University of Medicine and Pharmacy Craiova, University Medical Center Groningen, Universidad Peruana Cayetano Heredia
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1. Study Identification

Unique Protocol Identification Number
NCT02106039
Brief Title
Pulmonary Tuberculosis Patients With Diabetes Mellitus
Acronym
TANDEM
Official Title
Concurrent Tuberculosis and Diabetes: Clinical Monitoring, and Microbiological and Immunological Effects of Diabetes During Tuberculosis Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
April 28, 2014 (Actual)
Primary Completion Date
February 21, 2017 (Actual)
Study Completion Date
December 21, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitas Padjadjaran
Collaborators
London School of Hygiene and Tropical Medicine, Radboud University Medical Center, Leiden University Medical Center, University of Stellenbosch, St George's, University of London, University of Otago, University of Medicine and Pharmacy Craiova, University Medical Center Groningen, Universidad Peruana Cayetano Heredia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effect of enhanced glycemic monitoring of diabetes upon diabetes glycaemic control during tuberculosis treatment in tuberculosis- diabetes patients.
Detailed Description
Tight glycemic control may improve tuberculosis (TB) treatment outcome and help reduce symptoms. However, active TB and TB treatment hamper glycemic control. Patients starting TB treatment experience rapid changes in appetite, body composition, and inflammation (which increases insulin resistance); inflammation is a feature of untreated TB and following an increase as a result of initial bacterial killing, inflammation subsides with successful treatment. In addition, TB medication (rifampicin) increases the metabolism of oral anti-diabetic drugs including the widely used sulphonylureas and thiazolidinediones, though a possible interaction with the antidiabetic drug metformin has not been previously examined. Frequent monitoring of blood glucose with adjustments in anti-diabetes medication during the course of TB treatment may therefore be needed. However, frequent monitoring is associated with additional costs, and tools and skills for glucose monitoring and diabetes treatment may be lacking in TB or pulmonary clinics, creating a need to refer patients to other health providers. As such, a less intense schedule, preferably following the established decision points in TB treatment after 2 and 6 months would offer significant advantage. None of these issues have been addressed systematically so far.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Pulmonary Tuberculosis
Keywords
diabetes mellitus, tuberculosis, management, randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Actual)

8. Arms, Groups, and Interventions

Arm Title
intensive monitoring
Arm Type
Experimental
Arm Description
more intensive monitoring strategy of blood glucose and clinical review
Arm Title
standard monitoring
Arm Type
No Intervention
Arm Description
glucose monitoring followed the prevailing practice at each site
Intervention Type
Procedure
Intervention Name(s)
intensive monitoring
Primary Outcome Measure Information:
Title
Better diabetes control in diabetes patients with tuberculosis under treatment
Description
Diabetes control is determined by HbA1c level (unit: %) which will be measured at month 3 and 6 of TB treatment.
Time Frame
Up to 6 months during TB treatment
Secondary Outcome Measure Information:
Title
Cost-effectiveness of different strategies for diabetes management during TB treatment
Description
Cost analysis will include all cost for lab analysis, transportation for follow up visit, expenses for medications, all complications caused by uncontrolled diabetes (including hospitalization, medications for co morbidities)
Time Frame
Up to 6 months
Title
Measurement of long-term requirements for diabetes management in TB patients diagnosed with diabetes after TB treatment completed
Description
Clinical characteristics (i.e. blood pressure, glucose control, kidney function, quality of life (QoL) of diabetes mellitus patients with TB after completing TB treatment will be measured and will be compared between both groups.
Time Frame
12 months after completing TB treatment
Title
Association between glycemic control and clinical-microbiological response to TB treatment
Description
Association between glycemic control and clinical response to TB treatment will be determined by measuring: increasing of body weight, symptoms relieve, treatment outcome (cured, completed, failure and default), and will be compared between groups. Association between glycemic control and microbiological response to TB treatment will be determined by measuring sputum conversion time (time to negative culture), and will be compared between groups.
Time Frame
up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult (> 18 years old) diabetes mellitus patients diagnosed as having active pulmonary TB willing to join the study Exclusion Criteria: under TB treatment more than 72 hours steroid-induced or gestational diabetes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hazel Dockrell, Prof
Organizational Affiliation
LSHTM
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Reinout van Crevel, MD, PhD
Organizational Affiliation
Radboud Universisty Nijmegen Medical Center
Official's Role
Study Director
Facility Information:
Facility Name
Faculty of Medicine, Universitas Padjadjaran
City
Bandung
State/Province
West Java
ZIP/Postal Code
40161
Country
Indonesia
Facility Name
Universidad Peruana Cayetano Heredia
City
Lima
State/Province
San Martin De Porres
ZIP/Postal Code
31
Country
Peru
Facility Name
University of Medicine and Pharmacy Craiova
City
Bucharest
Country
Romania

12. IPD Sharing Statement

Citations:
PubMed Identifier
21722362
Citation
Baker MA, Harries AD, Jeon CY, Hart JE, Kapur A, Lonnroth K, Ottmani SE, Goonesekera SD, Murray MB. The impact of diabetes on tuberculosis treatment outcomes: a systematic review. BMC Med. 2011 Jul 1;9:81. doi: 10.1186/1741-7015-9-81.
Results Reference
background
PubMed Identifier
20955495
Citation
Ruslami R, Aarnoutse RE, Alisjahbana B, van der Ven AJ, van Crevel R. Implications of the global increase of diabetes for tuberculosis control and patient care. Trop Med Int Health. 2010 Nov;15(11):1289-99. doi: 10.1111/j.1365-3156.2010.02625.x.
Results Reference
background
PubMed Identifier
15034704
Citation
Bidstrup TB, Stilling N, Damkier P, Scharling B, Thomsen MS, Brosen K. Rifampicin seems to act as both an inducer and an inhibitor of the metabolism of repaglinide. Eur J Clin Pharmacol. 2004 Apr;60(2):109-14. doi: 10.1007/s00228-004-0746-z. Epub 2004 Mar 19.
Results Reference
background
PubMed Identifier
12817528
Citation
Hatorp V, Hansen KT, Thomsen MS. Influence of drugs interacting with CYP3A4 on the pharmacokinetics, pharmacodynamics, and safety of the prandial glucose regulator repaglinide. J Clin Pharmacol. 2003 Jun;43(6):649-60.
Results Reference
background
PubMed Identifier
16390353
Citation
Jaakkola T, Backman JT, Neuvonen M, Laitila J, Neuvonen PJ. Effect of rifampicin on the pharmacokinetics of pioglitazone. Br J Clin Pharmacol. 2006 Jan;61(1):70-8. doi: 10.1111/j.1365-2125.2005.02515.x.
Results Reference
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PubMed Identifier
12968988
Citation
Niemi M, Backman JT, Neuvonen M, Neuvonen PJ. Effect of rifampicin on the pharmacokinetics and pharmacodynamics of nateglinide in healthy subjects. Br J Clin Pharmacol. 2003 Oct;56(4):427-32. doi: 10.1046/j.1365-2125.2003.01884.x.
Results Reference
background
PubMed Identifier
11103752
Citation
Niemi M, Backman JT, Neuvonen M, Neuvonen PJ, Kivisto KT. Rifampin decreases the plasma concentrations and effects of repaglinide. Clin Pharmacol Ther. 2000 Nov;68(5):495-500. doi: 10.1067/mcp.2000.111183.
Results Reference
background
PubMed Identifier
11406737
Citation
Niemi M, Backman JT, Neuvonen M, Neuvonen PJ, Kivisto KT. Effects of rifampin on the pharmacokinetics and pharmacodynamics of glyburide and glipizide. Clin Pharmacol Ther. 2001 Jun;69(6):400-6. doi: 10.1067/mcp.2001.115822.
Results Reference
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PubMed Identifier
11136298
Citation
Niemi M, Kivisto KT, Backman JT, Neuvonen PJ. Effect of rifampicin on the pharmacokinetics and pharmacodynamics of glimepiride. Br J Clin Pharmacol. 2000 Dec;50(6):591-5. doi: 10.1046/j.1365-2125.2000.00295.x.
Results Reference
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PubMed Identifier
15001966
Citation
Park JY, Kim KA, Kang MH, Kim SL, Shin JG. Effect of rifampin on the pharmacokinetics of rosiglitazone in healthy subjects. Clin Pharmacol Ther. 2004 Mar;75(3):157-62. doi: 10.1016/j.clpt.2003.10.003.
Results Reference
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PubMed Identifier
14534520
Citation
Park JY, Kim KA, Park PW, Park CW, Shin JG. Effect of rifampin on the pharmacokinetics and pharmacodynamics of gliclazide. Clin Pharmacol Ther. 2003 Oct;74(4):334-40. doi: 10.1016/S0009-9236(03)00221-2.
Results Reference
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PubMed Identifier
1254383
Citation
Syvalahti E, Pihlajamaki K, Iisalo E. Effect of tuberculostatic agents on the response of serum growth hormone and immunoreactive insulin to intravenous tolbutamide, and on the half-life of tolbutamide. Int J Clin Pharmacol Biopharm. 1976 Mar;13(2):83-9.
Results Reference
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PubMed Identifier
1233266
Citation
Zilly W, Breimer DD, Richter E. Induction of drug metabolism in man after rifampicin treatment measured by increased hexobarbital and tolbutamide clearance. Eur J Clin Pharmacol. 1975 Dec 19;9(2-3):219-27. doi: 10.1007/BF00614021.
Results Reference
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Links:
URL
http://tandem-fp7.eu
Description
official website of TANDEM project

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Pulmonary Tuberculosis Patients With Diabetes Mellitus

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