isoniazid has been researched along with Hepatitis C in 9 studies
Hydra: A genus of freshwater polyps in the family Hydridae, order Hydroida, class HYDROZOA. They are of special interest because of their complex organization and because their adult organization corresponds roughly to the gastrula of higher animals.
hydrazide : Compounds derived from oxoacids RkE(=O)l(OH)m (l =/= 0) by replacing -OH by -NRNR2 (R groups are commonly H). (IUPAC).
Hepatitis C: INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown.
Excerpt | Relevance | Reference |
---|---|---|
"Treatment of latent Mycobacterium tuberculosis infection with isoniazid can cause hepatotoxicity, but the risk of isoniazid-associated hepatotoxicity among persons coinfected with hepatitis C virus (HCV) is unknown." | 7.71 | Isoniazid preventive therapy, hepatitis C virus infection, and hepatotoxicity among injection drug users infected with Mycobacterium tuberculosis. ( Astemborski, J; Bonds, M; Graham, NM; Madison, A; Sadaphal, P; Sheely, L; Sterling, TR; Thomas, DL; Vlahov, D, 2001) |
"Treatment with isoniazid in drug users appears to be safe and well tolerated, although frequent asymptomatic elevations in transaminase levels were observed." | 5.32 | Isoniazid hepatotoxicity among drug users: the role of hepatitis C. ( Fernández-Villar, A; Fluiters, E; Martínez-Vázquez, C; Mosteiro, M; Piñeiro, L; Sopeña, B; Ulloa, F; Vázquez, R, 2003) |
" Key recent developments to address HIV-related TB among PWIDs include the use of simplified symptom-based algorithm to provide isoniazid-preventive therapy, molecular DNA detection methods for Mycobacterium tuberculosis and the immediate provision of antiretroviral therapy within the first 2 weeks of initiation of anti-TB treatment." | 4.88 | Tuberculosis and HIV in people who inject drugs: evidence for action for tuberculosis, HIV, prison and harm reduction services. ( Getahun, H; Gunneberg, C; Raviglione, M; Sculier, D; Verster, A, 2012) |
"Treatment of latent Mycobacterium tuberculosis infection with isoniazid can cause hepatotoxicity, but the risk of isoniazid-associated hepatotoxicity among persons coinfected with hepatitis C virus (HCV) is unknown." | 3.71 | Isoniazid preventive therapy, hepatitis C virus infection, and hepatotoxicity among injection drug users infected with Mycobacterium tuberculosis. ( Astemborski, J; Bonds, M; Graham, NM; Madison, A; Sadaphal, P; Sheely, L; Sterling, TR; Thomas, DL; Vlahov, D, 2001) |
"Serologic markers for hepatitis viruses were studied in 40 children who developed acute hepatitis during antituberculosis therapy with rifampin and isoniazid, with the aim of assessing the contributory role of these viruses toward producing hepatic injury." | 3.68 | Hepatotoxicity of rifampin and isoniazid. Is it all drug-induced hepatitis? ( Govil, YC; Kumar, A; Mehotra, R; Misra, PK; Rana, GS, 1991) |
"Treatment with isoniazid in drug users appears to be safe and well tolerated, although frequent asymptomatic elevations in transaminase levels were observed." | 1.32 | Isoniazid hepatotoxicity among drug users: the role of hepatitis C. ( Fernández-Villar, A; Fluiters, E; Martínez-Vázquez, C; Mosteiro, M; Piñeiro, L; Sopeña, B; Ulloa, F; Vázquez, R, 2003) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (22.22) | 18.2507 |
2000's | 4 (44.44) | 29.6817 |
2010's | 3 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Adamu, B | 1 |
Abdu, A | 1 |
Abba, AA | 1 |
Borodo, MM | 1 |
Tleyjeh, IM | 1 |
Bliven-Sizemore, EE | 1 |
Sterling, TR | 2 |
Shang, N | 1 |
Benator, D | 1 |
Schwartzman, K | 1 |
Reves, R | 1 |
Drobeniuc, J | 1 |
Bock, N | 1 |
Villarino, ME | 1 |
Getahun, H | 1 |
Gunneberg, C | 1 |
Sculier, D | 1 |
Verster, A | 1 |
Raviglione, M | 1 |
Fernández-Villar, A | 2 |
Sopeña, B | 2 |
Vázquez, R | 1 |
Ulloa, F | 1 |
Fluiters, E | 1 |
Mosteiro, M | 1 |
Martínez-Vázquez, C | 1 |
Piñeiro, L | 1 |
Valencia Ortega, ME | 1 |
Leiro, V | 1 |
Botana, M | 1 |
Türktaş, H | 1 |
Unsal, M | 1 |
Tülek, N | 1 |
Orüç, O | 1 |
Sadaphal, P | 1 |
Astemborski, J | 1 |
Graham, NM | 1 |
Sheely, L | 1 |
Bonds, M | 1 |
Madison, A | 1 |
Vlahov, D | 1 |
Thomas, DL | 1 |
Kumar, A | 1 |
Misra, PK | 1 |
Mehotra, R | 1 |
Govil, YC | 1 |
Rana, GS | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
One-month Latent Tuberculosis Treatment for Renal Transplant Candidates[NCT05411744] | Phase 4 | 25 participants (Anticipated) | Interventional | 2022-07-01 | Recruiting | ||
URBAN ARCH (3/5) Uganda Cohort TB Preventive Therapy for HIV-infected Alcohol Users in Uganda: an Evaluation of Safety Tolerability and Adherence[NCT03302299] | Phase 4 | 302 participants (Actual) | Interventional | 2017-04-07 | Completed | ||
Efficacy of Risk-Targeted Video Based Directly on Observed Therapy for Latent TB[NCT03783728] | 0 participants (Actual) | Observational | 2019-06-30 | Withdrawn (stopped due to Investigator is leaving the University) | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Safety will be assessed by the occurrence of a Grade 3/4 hepatotoxicity at any time during the assigned treatment period. (NCT03302299)
Timeframe: Hepatotoxicity occurring during the six month course (180 pills) of isoniazid (INH), which may be taken over a maximum of 9 months.
Intervention | percent (Number) |
---|---|
INH and Vitamin B6 | 8.3 |
Lack of tolerability will be defined as any isoniazid (INH) treatment discontinuation prior to completion of the prescribed course (6 months of INH taken over a maximum period of 9 months) due to side effects or alanine transaminase (ALT)/aspartate transaminase (AST) elevations. (NCT03302299)
Timeframe: Six month course (180 pills) of isoniazid (INH), which may be taken over a maximum of 9 months.
Intervention | Participants (Count of Participants) |
---|---|
INH and Vitamin B6 | 32 |
Alanine transaminase (ALT) or aspartate transaminase (AST) elevations (>2x the upper limit of normal) at study screening (NCT03302299)
Timeframe: Study screening visit
Intervention | Participants (Count of Participants) |
---|---|
Study Screening | 80 |
Latent tuberculosis assessed at screening via tuberculin skin testing (TST). A TST induration >=5mm was considered positive for latent tuberculosis. (NCT03302299)
Timeframe: Study screening visit
Intervention | Participants (Count of Participants) |
---|---|
Study Screening | 308 |
INH concentration in hair (pmol/mg) will be measured at 3- and 6- months during INH therapy. (NCT03302299)
Timeframe: Measured at 3- and 6- months after INH initiation
Intervention | pmol/mg (Median) | |
---|---|---|
at 3 months | at 6 months | |
INH and Vitamin B6 | 36.0 | 37.8 |
Suboptimal INH adherence was defined as <90% of days with at least 1 electronic medication management (EMM) pill cap opening in the previous 90 days, at 3- and 6-months. (NCT03302299)
Timeframe: Adherence will be measured over the 6 months on INH or until INH discontinuation (whichever is shorter)
Intervention | percentage of participants (Number) | |
---|---|---|
at 3 months | at 6 months | |
INH and Vitamin B6 | 31.3 | 43.9 |
"Participants were asked In the past 30 days, how many days in total have you not taken your pill? and were presented with a visual analog scale (VAS) to indicate the percentage of INH taken in the past 30 days. We converted the VAS percentage into number of days out of 30 to match the first question. Our final self-report measure was the minimum number of the 2 self-reported measurements." (NCT03302299)
Timeframe: Self-reported INH medication adherence via VAS will be measured 3- and 6- months after starting INH
Intervention | days (Median) | |
---|---|---|
at 3 months | at 6 months | |
INH and Vitamin B6 | 30 | 30 |
The Self Rating Single Item (SRSI) adherence scale asks participants to rate their ability to take their medications as prescribed over the past 30 days. Participants reporting INH use in the prior 30 days at the 3- or 6-month interview are included here, and reported their INH adherence in the prior 30 days as excellent, very good, good, fair, poor, or very poor. (NCT03302299)
Timeframe: Self-reported INH medication adherence via SRSI will be measured 3- and 6- months after starting INH
Intervention | Participants (Count of Participants) | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
At 3 months72558043 | At 6 months72558043 | |||||||||||
Excellent | Very good | Good | Fair | Poor | Very poor | |||||||
INH and Vitamin B6 | 160 | |||||||||||
INH and Vitamin B6 | 79 | |||||||||||
INH and Vitamin B6 | 38 | |||||||||||
INH and Vitamin B6 | 2 | |||||||||||
INH and Vitamin B6 | 124 | |||||||||||
INH and Vitamin B6 | 90 | |||||||||||
INH and Vitamin B6 | 41 | |||||||||||
INH and Vitamin B6 | 4 | |||||||||||
INH and Vitamin B6 | 0 | |||||||||||
INH and Vitamin B6 | 1 |
2 reviews available for isoniazid and Hepatitis C
Article | Year |
---|---|
Antibiotic prophylaxis for preventing post solid organ transplant tuberculosis.
Topics: Antibiotic Prophylaxis; Antitubercular Agents; Chemical and Drug Induced Liver Injury; Hepatitis B; | 2014 |
Tuberculosis and HIV in people who inject drugs: evidence for action for tuberculosis, HIV, prison and harm reduction services.
Topics: Antitubercular Agents; Chemoprevention; Comorbidity; Harm Reduction; Hepatitis B; Hepatitis C; HIV I | 2012 |
1 trial available for isoniazid and Hepatitis C
Article | Year |
---|---|
Three months of weekly rifapentine plus isoniazid is less hepatotoxic than nine months of daily isoniazid for LTBI.
Topics: Adult; Antitubercular Agents; Aspartate Aminotransferases; Brazil; Canada; Case-Control Studies; Che | 2015 |
Three months of weekly rifapentine plus isoniazid is less hepatotoxic than nine months of daily isoniazid for LTBI.
Topics: Adult; Antitubercular Agents; Aspartate Aminotransferases; Brazil; Canada; Case-Control Studies; Che | 2015 |
Three months of weekly rifapentine plus isoniazid is less hepatotoxic than nine months of daily isoniazid for LTBI.
Topics: Adult; Antitubercular Agents; Aspartate Aminotransferases; Brazil; Canada; Case-Control Studies; Che | 2015 |
Three months of weekly rifapentine plus isoniazid is less hepatotoxic than nine months of daily isoniazid for LTBI.
Topics: Adult; Antitubercular Agents; Aspartate Aminotransferases; Brazil; Canada; Case-Control Studies; Che | 2015 |
6 other studies available for isoniazid and Hepatitis C
Article | Year |
---|---|
Isoniazid hepatotoxicity among drug users: the role of hepatitis C.
Topics: Adolescent; Adult; Antitubercular Agents; Female; Hepatitis C; Humans; Isoniazid; Liver; Male; Middl | 2003 |
[Medicine and television: a diagnosis history].
Topics: Adult; Antitubercular Agents; Cholestasis, Intrahepatic; Diagnostic Errors; Hepatitis B; Hepatitis C | 2005 |
Hepatitis C virus infection and isoniazid hepatotoxicity.
Topics: Antitubercular Agents; Hepatitis C; Humans; Isoniazid; Liver; Prognosis; Risk Factors; Substance-Rel | 2007 |
Hepatotoxicity of antituberculosis therapy (rifampicin, isoniazid and pyrazinamide) or viral hepatitis.
Topics: Acute Disease; Adolescent; Adult; Chemical and Drug Induced Liver Injury; Diagnosis, Differential; D | 1994 |
Isoniazid preventive therapy, hepatitis C virus infection, and hepatotoxicity among injection drug users infected with Mycobacterium tuberculosis.
Topics: Adult; Antibiotic Prophylaxis; Antitubercular Agents; Chemical and Drug Induced Liver Injury; Female | 2001 |
Hepatotoxicity of rifampin and isoniazid. Is it all drug-induced hepatitis?
Topics: Chemical and Drug Induced Liver Injury; Child; Child, Preschool; Female; Hepatitis A; Hepatitis B; H | 1991 |