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Treatment Duration for Abdominal Tuberculosis (RNTCP-DOTS)

Primary Purpose

Tuberculosis

Status
Completed
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
RNTCP Category I treatment for 6 months
RNTCP Category I treatment for 9months
Sponsored by
All India Institute of Medical Sciences, New Delhi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tuberculosis focused on measuring Intestinal tuberculosis, Tuberculous peritonitis, Abdominal tuberculosis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria:

  • Newly diagnosed patients with Intestinal TB or Peritoneal TB
  • Has not received ATT for Tuberculosis any where in the body during past 5 years
  • Patients having good general health and not too sick.
  • Patients willing and likely to comply with the study procedures and follow up
  • Patients should give informed consent.

Exclusion Criteria:

  • Eighteen year is a cut off age for definition of adult and pediatric and adolescent medicine. The dosing of drugs are different in these two age groups. Therefore we plan to include patients of more than 18 years of age with abdominal TB in this study.
  • Intake of ATT during the past 5 years
  • Doubtful diagnosis
  • Crohn's disease
  • Patients with HIV and AIDS may have another systemic opportunistic infections including GI infections like cryptosporidiosis, Microsporidiosis or isosporiasis. There may be an overlap of GI manifestations such as diarrhea, abdominal pain, anemia, fever. Therefore, assessment of response to anti-tuberculosis therapy may be blurred. In order to keep the study group homogenous for comparison, we plan to exclude all those with HIV infection
  • Chronic Liver Disease
  • Associated significant co-morbidities
  • H/O Sensitivity
  • Peritoneal carcinomatosis
  • Patients must not been used investigational agents during the past 6 months
  • Unwilling patient

Sites / Locations

  • Dr Govind K Makharia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Arm 1: Category I treatment for 6 months

Arm 2: Category I treatment for 9 months

Arm Description

Anti-tuberculosis drugs

Anti-tuberculosis drugs,

Outcomes

Primary Outcome Measures

Response to treatment (after 6 months and nine months of RNTCP Category I treatment)
Intestinal tuberculosis: Complete response to treatment: Resolution of clinical manifestations, Healing of demonstrable lesions, Microbiological response (Conversion of positive to negative) Clinical failure: Failure of response to treatment: Persistence of clinical manifestations Persistence of morphological lesions Peritoneal tuberculosis: Definition for response Complete response: Complete resolution of ascites within 6 months No response: Persistence of ascites
Recurrence of symptoms of abdominal tuberculosis (intestinal and peritoneal) after 1 year of follow up in those who receive 6 months or 9 months of Cat I treatment

Secondary Outcome Measures

Full Information

First Posted
May 3, 2010
Last Updated
July 2, 2015
Sponsor
All India Institute of Medical Sciences, New Delhi
Collaborators
Sanjay Gandhi Postgraduate Institute of Medical Sciences, Christian Medical College, Vellore, India
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1. Study Identification

Unique Protocol Identification Number
NCT01124929
Brief Title
Treatment Duration for Abdominal Tuberculosis
Acronym
RNTCP-DOTS
Official Title
A Multi-centric Study on Treatment of Abdominal Tuberculosis (Intestinal or Peritoneal): A Randomized Controlled Trial to Compare the 6 Months of Cat I Treatment With 9 Months of Cat I Treatment (Extension for 3 Months) in Abdominal Tuberculosis Under the Revised National Tuberculosis Control Program
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
April 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, New Delhi
Collaborators
Sanjay Gandhi Postgraduate Institute of Medical Sciences, Christian Medical College, Vellore, India

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Most of the guidelines on the treatment of tuberculosis suggest that 6 months treatment is sufficient for extrapulmonary tuberculosis except for bone tuberculosis and tubercular meningitis. Despite these recommendations, most physicians treating abdominal tuberculosis use antituberculous therapy for 9 months, sometimes even 12 months without any scientific justification. In a randomized controlled trial, Balasubramaniam et al reported no difference in success rate of 6mo (99%) vs 12 months (94%) antituberculous drugs (conventional strategy) in the treatment of abdominal tuberculosis. Although Directly Observed Therapy (DOTs) have been proved to be effective in patients with pulmonary tuberculosis, lymph nodal tuberculosis, however, there is a lack of data on efficacy of DOTS in other extra-pulmonary disease including abdominal tuberculosis. Therefore, there is an urgent need to establish the efficacy of DOTs strategy of antituberculous therapy in the treatment of abdominal tuberculosis. Therefore, the investigators planned to conduct a multicenter randomized controlled trial to determine the difference in the recurrence of disease after only observation for three months and three months extension of DOTs in a subset of patients with definite clinical response after 6 months of DOTs.
Detailed Description
Rationale Most of the guidelines on the treatment of tuberculosis suggest that 6 months treatment is sufficient for extrapulmonary tuberculosis except for bone tuberculosis and tubercular meningitis. Despite these recommendations, most physicians treating abdominal tuberculosis use antituberculous therapy for 9 months, sometimes even 12 months without any scientific justification. In a randomized controlled trial, Balasubramaniam et al reported no difference in success rate of 6mo (99%) vs 12 months (94%) antituberculous drugs (conventional strategy) in the treatment of abdominal tuberculosis. Although DOTS have been proved to be effective in patients with pulmonary tuberculosis, lymph nodal tuberculosis, however, there is a lack of data on efficacy of DOTS in other extra-pulmonary disease including abdominal tuberculosis. The aim of the present study is not to assess the efficacy of DOTs but whether the Cat I regimen for 6 months is effective in the treatment of abdominal tuberculosis. We, therefore planned to conduct a multicenter randomized controlled trial to determine the difference in the efficacy and recurrence rate in 6months and 9 months of intermittent short course category I regimen under RNTCP. Hypothesis There may not be a significant difference in the efficacy and recurrence rate of abdominal tuberculosis in those treated for six months vs those treated for 9 months with intermittent short course category I regimen under RNTCP. Objectives Primary objectives: To determine the efficacy of intermittent short course chemotherapy for 6 months under Directly Observed Therapy (Category I under RNTCP) in treatment of abdominal tuberculosis (proportion of patients responding to treatment) To determine difference in the recurrence of disease between the two randomized groups after only observation for three months and extension of RNTCP Cat I for three months in a subset of patients with definite clinical response after 6 months of DOTs Secondary objective 1. To study the effect of anti-tubercular drugs on the natural history of intestinal stricture due to tuberculosis Outcomes Outcome measures: Primary: Response to treatment (6 months and nine months of RNTCP Cat I treatment) as defined earlier Recurrence of symptoms of abdominal tuberculosis (intestinal and peritoneal) after 1 year of follow up in those who receive 6 months or 9 months of Cat I treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
Intestinal tuberculosis, Tuberculous peritonitis, Abdominal tuberculosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
197 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1: Category I treatment for 6 months
Arm Type
Active Comparator
Arm Description
Anti-tuberculosis drugs
Arm Title
Arm 2: Category I treatment for 9 months
Arm Type
Active Comparator
Arm Description
Anti-tuberculosis drugs,
Intervention Type
Drug
Intervention Name(s)
RNTCP Category I treatment for 6 months
Intervention Description
2H3R3Z3 E3 + 4H3R3
Intervention Type
Drug
Intervention Name(s)
RNTCP Category I treatment for 9months
Intervention Description
2H3R3Z3 E3 + 7H3R3
Primary Outcome Measure Information:
Title
Response to treatment (after 6 months and nine months of RNTCP Category I treatment)
Description
Intestinal tuberculosis: Complete response to treatment: Resolution of clinical manifestations, Healing of demonstrable lesions, Microbiological response (Conversion of positive to negative) Clinical failure: Failure of response to treatment: Persistence of clinical manifestations Persistence of morphological lesions Peritoneal tuberculosis: Definition for response Complete response: Complete resolution of ascites within 6 months No response: Persistence of ascites
Time Frame
1 year
Title
Recurrence of symptoms of abdominal tuberculosis (intestinal and peritoneal) after 1 year of follow up in those who receive 6 months or 9 months of Cat I treatment
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria: Newly diagnosed patients with Intestinal TB or Peritoneal TB Has not received ATT for Tuberculosis any where in the body during past 5 years Patients having good general health and not too sick. Patients willing and likely to comply with the study procedures and follow up Patients should give informed consent. Exclusion Criteria: Eighteen year is a cut off age for definition of adult and pediatric and adolescent medicine. The dosing of drugs are different in these two age groups. Therefore we plan to include patients of more than 18 years of age with abdominal TB in this study. Intake of ATT during the past 5 years Doubtful diagnosis Crohn's disease Patients with HIV and AIDS may have another systemic opportunistic infections including GI infections like cryptosporidiosis, Microsporidiosis or isosporiasis. There may be an overlap of GI manifestations such as diarrhea, abdominal pain, anemia, fever. Therefore, assessment of response to anti-tuberculosis therapy may be blurred. In order to keep the study group homogenous for comparison, we plan to exclude all those with HIV infection Chronic Liver Disease Associated significant co-morbidities H/O Sensitivity Peritoneal carcinomatosis Patients must not been used investigational agents during the past 6 months Unwilling patient
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Govind K Makharia, MD, DM, DNB
Organizational Affiliation
All India Institute of Medical Sciences, New Delhi
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr Govind K Makharia
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110029
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
25969531
Citation
Makharia GK, Ghoshal UC, Ramakrishna BS, Agnihotri A, Ahuja V, Chowdhury SD, Gupta SD, Mechenro J, Mishra A, Mishra A, Pathak MK, Pandey RM, Sharma R, Sharma SK. Intermittent Directly Observed Therapy for Abdominal Tuberculosis: A Multicenter Randomized Controlled Trial Comparing 6 Months Versus 9 Months of Therapy. Clin Infect Dis. 2015 Sep 1;61(5):750-7. doi: 10.1093/cid/civ376. Epub 2015 May 12.
Results Reference
derived

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Treatment Duration for Abdominal Tuberculosis

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