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Diagnostic Tools for Human African Trypanosomiasis Elimination and Clinical Trials: Early Test-of-cure (DiTECT-WP4)

Primary Purpose

African Trypanosomiasis, African; Trypanosomiasis, West, Sleeping Sickness; West African

Status
Completed
Phase
Not Applicable
Locations
Congo, The Democratic Republic of the
Study Type
Interventional
Intervention
RNA and neopterin detection
Sponsored by
Institut de Recherche pour le Developpement
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for African Trypanosomiasis focused on measuring diagnosis, sensitivity, specificity, therapeutic outcome, cerebrospinal fluid

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Eligible for participation in DNDi-OXA-02-HAT clinical trial

Exclusion Criteria:

  • Excluded for DNDi-OXA-02-HAT clinical trial; No informed consent for participation in the DiTECT-HAT-WP4 study

Sites / Locations

  • Programme Nationale de Lutte contre la trypanosomiase humaine Africaine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Human african trypanosomiasis patient

Arm Description

RNA, neopterin and 5-hydroxytryptophan detection

Outcomes

Primary Outcome Measures

Sensitivity of SL-RNA detection in blood, SL-RNA detection in cerebrospinal fluid and of neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid for relapse after human African trypanosomiasis treatment
Index tests: qualitative detection of SL-RNA in blood, qualitative detection of SL-RNA in cerebrospinal fluid, neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid. Reference standard: classification according to the WHO 2015 criteria as relapse or probable relapse within 18 months after treatment for human African trypanosomiasis
Specificity of SL-RNA detection in blood, SL-RNA detection in cerebrospinal fluid and of neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid for cure after human African trypanosomiasis treatment
Index tests: qualitative detection of SL-RNA in blood, qualitative detection of SL-RNA in cerebrospinal fluid, neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid. Reference standard: classification according to the WHO 2015 criteria as cure or probable cure 18 months after treatment

Secondary Outcome Measures

Sensitivity and specificity SL-RNA detection in blood for outcome assesment after treatment for human African trypanosomiasis
Index tests: qualitative detection of SL-RNA in blood post treatment day 11, month 6, month 12 and month 18. Reference standard: Human African trypanosomiasis treatment outcome classification according to the WHO 2015 criteria
Sensitivity and specificity SL-RNA detection in cerebrospinal fluid for outcome assesment after treatment for human African trypanosomiasis
Index tests: qualitative detection of SL-RNA in cerebrospinal fluid at post treatment day 11, month 6, month 12 and month 18. Reference standard: Human African trypanosomiasis treatment outcome classification according to the WHO 2015 criteria
Sensitivity and specificity by ROC analysis of neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid for outcome assesment after treatment for human African trypanosomiasis
Index tests: quantitative detection of neopterin & 5-hydroxytryptophan in cerebrospinal fluid at post treatment day 11, month 6, month 12 and month 18. Reference standard: Human African trypanosomiasis treatment outcome classification according to the WHO 2015 criteria

Full Information

First Posted
March 31, 2017
Last Updated
February 18, 2021
Sponsor
Institut de Recherche pour le Developpement
Collaborators
Institute of Tropical Medicine, Belgium, Institut National de Recherche Biomédicale. Kinshasa, République Démocratique du Congo, Ministry of Public Health, Democratic Republic of the Congo
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1. Study Identification

Unique Protocol Identification Number
NCT03112655
Brief Title
Diagnostic Tools for Human African Trypanosomiasis Elimination and Clinical Trials: Early Test-of-cure
Acronym
DiTECT-WP4
Official Title
Diagnostic Tools for Human African Trypanosomiasis Elimination and Clinical Trials: WP4 Early Test-of-cure
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
February 24, 2017 (Actual)
Primary Completion Date
January 31, 2021 (Actual)
Study Completion Date
January 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut de Recherche pour le Developpement
Collaborators
Institute of Tropical Medicine, Belgium, Institut National de Recherche Biomédicale. Kinshasa, République Démocratique du Congo, Ministry of Public Health, Democratic Republic of the Congo

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
The study validates the diagnostic performance of cerebrospinal fluid neopterin quantification and of blood and cerebrospinal fluid trypanosomal spliced leader RNA detection for assessing outcome after treatment of human African trypanosomiasis.
Detailed Description
In the last decade, the prevalence of Trypanosoma brucei gambiense human African trypanosomiasis (HAT) has fallen and HAT has been targeted for elimination. Development of safe and efficacious drugs for HAT, applicable in an elimination context, is considered as a high priority. The drug developmental process is however slowed down by the need to follow-up treated patients for 18 months to decide on cure. For timely diagnosis of treatment failure in clinical trials, patients should have control visits with follow-up examinations at 6, 12 and 18 months after treatment. Furthermore, due to repeated lumbar punctures, treated patients refrain to present for control visits spontaneously, and tend not to comply with follow-up. Clinical trials on new drugs for HAT would therefore be accelerated by availability of an early test of cure. Trypanosomal spliced leader (SL)-RNA, neopterin & 5-hydroxytryptophan are good candidates for accurate and shortened treatment follow-up. In particular SL-RNA detection in blood offers an opportunity for non-invasive post-treatment follow-up. The objective of the DiTECT-HAT-WP4 study is to validate the diagnostic performance of cerebrospinal fluid neopterin & 5-hydroxytryptophan quantification and of blood and cerebrospinal fluid trypanosomal spliced leader RNA detection for assessing treatment outcome. The DiTECT-HAT-WP4 study is embedded into an ongoing therapeutic phase II/III study (DNDi-OXA-02-HAT) testing a new oral single dose drug against HAT. Within the Framework of the therapeutical trial, patients will have post-treatment examinations, including blood and cerebrospinal fluid examination at day 11, and during follow-up at month 6, month 12 and month 18. Combination of DiTECT-HAT-WP4 with this ongoing clinical trial allows evaluation of new treatment outcome assessment markers during follow-up without the need for additional lumbar or venipunctures. The volumes of venous blood and cerebrospinal fluid taken will be increased by 2.5 mls for the DiTECT-HAT-WP4 study. Reverse transcriptase real time PCR for spliced leader RNA detection in blood and cerebrospinal fluid and neopterin detection will be carried out in the reference laboratory in Kinshasa, (index tests). The reference laboratory will be blinded to the results of the reference standard. For evaluation of diagnostic performance of the index tests, the reference standard will consist of classification of treatment outcome according to international standards applied for the clinical trial. Receiver operator curves, sensitivity and specificity of the different index tests for treatment outcome assessment will be determined at each follow-up time point. If sufficiently accurate, trypanosomal spliced leader RNA detection in blood would allow post-treatment follow-up without the need for lumbar punctures. Improved treatment outcome assessment will not only facilitate follow-up by avoiding the feared lumbar puncture but also speed up the development and implementation of new drugs. In addition, it will also improve management of patients in routine. The proposed research will impact on clinical decision and treatment outcomes, and contribute to successful HAT elimination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
African Trypanosomiasis, African; Trypanosomiasis, West, Sleeping Sickness; West African, Trypanosoma Brucei Gambiense; Infection
Keywords
diagnosis, sensitivity, specificity, therapeutic outcome, cerebrospinal fluid

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Masking Description
The reference laboratory, generating the results for the index test, is masked for results obtained at the clinical trial site (determining the standard reference).
Allocation
N/A
Enrollment
88 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Human african trypanosomiasis patient
Arm Type
Experimental
Arm Description
RNA, neopterin and 5-hydroxytryptophan detection
Intervention Type
Diagnostic Test
Intervention Name(s)
RNA and neopterin detection
Other Intervention Name(s)
Reverse transcriptase real-time PCR Trypanozoon SL-RNA, Neopterin & 5-hydroxytryptophan EIA, Mybiosource
Intervention Description
Detection of spliced leader RNA will be performed on blood and cerebrospinal fluid taken before treatment, 11 days after treatment, 6, 12 and 18 months after treatment. Neopterin and 5-hydroxytryptophan will be quantified in cerebrospinal fluid taken at the same time points.
Primary Outcome Measure Information:
Title
Sensitivity of SL-RNA detection in blood, SL-RNA detection in cerebrospinal fluid and of neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid for relapse after human African trypanosomiasis treatment
Description
Index tests: qualitative detection of SL-RNA in blood, qualitative detection of SL-RNA in cerebrospinal fluid, neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid. Reference standard: classification according to the WHO 2015 criteria as relapse or probable relapse within 18 months after treatment for human African trypanosomiasis
Time Frame
18 months
Title
Specificity of SL-RNA detection in blood, SL-RNA detection in cerebrospinal fluid and of neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid for cure after human African trypanosomiasis treatment
Description
Index tests: qualitative detection of SL-RNA in blood, qualitative detection of SL-RNA in cerebrospinal fluid, neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid. Reference standard: classification according to the WHO 2015 criteria as cure or probable cure 18 months after treatment
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Sensitivity and specificity SL-RNA detection in blood for outcome assesment after treatment for human African trypanosomiasis
Description
Index tests: qualitative detection of SL-RNA in blood post treatment day 11, month 6, month 12 and month 18. Reference standard: Human African trypanosomiasis treatment outcome classification according to the WHO 2015 criteria
Time Frame
post treatment day 11, month 6, month 12 and month 18
Title
Sensitivity and specificity SL-RNA detection in cerebrospinal fluid for outcome assesment after treatment for human African trypanosomiasis
Description
Index tests: qualitative detection of SL-RNA in cerebrospinal fluid at post treatment day 11, month 6, month 12 and month 18. Reference standard: Human African trypanosomiasis treatment outcome classification according to the WHO 2015 criteria
Time Frame
post treatment day 11, month 6, month 12 and month 18
Title
Sensitivity and specificity by ROC analysis of neopterin & 5-hydroxytryptophan quantification in cerebrospinal fluid for outcome assesment after treatment for human African trypanosomiasis
Description
Index tests: quantitative detection of neopterin & 5-hydroxytryptophan in cerebrospinal fluid at post treatment day 11, month 6, month 12 and month 18. Reference standard: Human African trypanosomiasis treatment outcome classification according to the WHO 2015 criteria
Time Frame
post treatment day 11, month 6, month 12 and month 18

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eligible for participation in DNDi-OXA-02-HAT clinical trial Exclusion Criteria: Excluded for DNDi-OXA-02-HAT clinical trial; No informed consent for participation in the DiTECT-HAT-WP4 study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Veerle Lejon, PhD
Organizational Affiliation
Institut de Recherche pour le Developpement
Official's Role
Principal Investigator
Facility Information:
Facility Name
Programme Nationale de Lutte contre la trypanosomiase humaine Africaine
City
Kinshasa
Country
Congo, The Democratic Republic of the

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24814957
Citation
Gonzalez-Andrade P, Camara M, Ilboudo H, Bucheton B, Jamonneau V, Deborggraeve S. Diagnosis of trypanosomatid infections: targeting the spliced leader RNA. J Mol Diagn. 2014 Jul;16(4):400-4. doi: 10.1016/j.jmoldx.2014.02.006. Epub 2014 May 9.
Results Reference
background
PubMed Identifier
26080371
Citation
Ilboudo H, Camara O, Ravel S, Bucheton B, Lejon V, Camara M, Kabore J, Jamonneau V, Deborggraeve S. Trypanosoma brucei gambiense Spliced Leader RNA Is a More Specific Marker for Cure of Human African Trypanosomiasis Than T. b. gambiense DNA. J Infect Dis. 2015 Dec 15;212(12):1996-8. doi: 10.1093/infdis/jiv337. Epub 2015 Jun 16.
Results Reference
background
PubMed Identifier
23469311
Citation
Tiberti N, Lejon V, Hainard A, Courtioux B, Robin X, Turck N, Kristensson K, Matovu E, Enyaru JC, Mumba Ngoyi D, Krishna S, Bisser S, Ndung'u JM, Buscher P, Sanchez JC. Neopterin is a cerebrospinal fluid marker for treatment outcome evaluation in patients affected by Trypanosoma brucei gambiense sleeping sickness. PLoS Negl Trop Dis. 2013;7(2):e2088. doi: 10.1371/journal.pntd.0002088. Epub 2013 Feb 28.
Results Reference
background
PubMed Identifier
27941966
Citation
Vincent IM, Daly R, Courtioux B, Cattanach AM, Bieler S, Ndung'u JM, Bisser S, Barrett MP. Metabolomics Identifies Multiple Candidate Biomarkers to Diagnose and Stage Human African Trypanosomiasis. PLoS Negl Trop Dis. 2016 Dec 12;10(12):e0005140. doi: 10.1371/journal.pntd.0005140. eCollection 2016 Dec.
Results Reference
background
PubMed Identifier
34534223
Citation
Ngay Lukusa I, Van Reet N, Mumba Ngoyi D, Miaka EM, Masumu J, Patient Pyana P, Mutombo W, Ngolo D, Kobo V, Akwaso F, Ilunga M, Kaninda L, Mutanda S, Muamba DM, Valverde Mordt O, Tarral A, Rembry S, Buscher P, Lejon V. Trypanosome SL-RNA detection in blood and cerebrospinal fluid to demonstrate active gambiense human African trypanosomiasis infection. PLoS Negl Trop Dis. 2021 Sep 17;15(9):e0009739. doi: 10.1371/journal.pntd.0009739. eCollection 2021 Sep.
Results Reference
derived
Links:
URL
http://apps.who.int/iris/bitstream/10665/173583/1/9789241508834_eng.pdf?ua=1
Description
Human African trypanosomiasis: update of the methodological framework for clinical trials
URL
https://clinicaltrials.gov/ct2/show/NCT01533961
Description
phase 1 study of drug now in phase 2/3

Learn more about this trial

Diagnostic Tools for Human African Trypanosomiasis Elimination and Clinical Trials: Early Test-of-cure

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