High vs. Standard Dose Rifampicin for Effusive Tuberculous Pericarditis

Официальное название

IMPI-3 - A Randomized Controlled Trial of High vs. Standard Dose Rifampicin for Effusive Tuberculous Pericarditis

Обзор

The investigators hypothesise that high dose RIF (RIF35) will increase pericardial fluid RIF exposure and so enhance mycobacterial clearance, compared to standard of care dosing (RIF10). This Phase 2b randomized, placebo-controlled, double-blinded trial will evaluate the efficacy and safety of RIF 35mg/kg compared 10mg/kg, added to standard first-line ATT, for the treatment of PCTB.

Подробное описание

IMPI-3 - A Randomized Controlled Trial of High vs. Standard Dose Rifampicin for Effusive Tuberculous Pericarditis

Phase 2b Randomized, placebo-controlled, double-blinded clinical trial

The trial will enroll 100 adult participants with pericardial TB from two research sites in South Africa, with no exclusions being made on the basis of sex/gender, racial or ethnic group.

Consenting participants will be stratified by HIV status and PCF GX-Ultra status, then randomized 1:1 to receive either standard of care anti-tuberculosis treatment (ATT) or standard of care plus high dose Rifampicin (RIF), both administered orally for 2 months, followed by a continuation phase of 4 months' RH at standard doses.

Вмешательства

• Препарат high dose Rifampicin (RIF)
  Simulations were performed to determine the dose of RIF required to achieve the most equitable drug exposures across the weight range, 30 to 100 kg. Demographic data of a reference cohort of TB patients (n = 1225), with or without HIV-1 coinfection, recruited in clinical trials conducted in West Africa and South Africa were used for the simulations35-38. An additional 12 250 virtual patients were generated using the weight and height distributions of the 1225 patients to increase the number of p

Первичные конечные точки

• Drug exposure in PCF and mediates in Mtb load [Срок оценки: 72 hours and 52 weeks]

Вторичные конечные точки (5)

• Mortality between study arms [Срок оценки: week 8 and 52 weeks]
• re-accumulation of pericardial effusion between study arms [Срок оценки: 52 weeks]
• TB-IRIS between study arms [Срок оценки: 52 weeks]
• Constrictive pericarditis between the study arms [Срок оценки: 52 weeks]
• CMR evidence [Срок оценки: 52 weeks]

Критерии участия

Критерии включения

• Aged >18 years
• Suspected PCTB with confirmed pericardial effusion on echocardiography (i.e., echo free space of ≥1 cm anterior to the right ventricle in diastole)
• Consent to study participation including testing for HIV-1 (if HIV status is unknown)
• Microbiologically detected Mtb in PCF or diagnosis of probable PCTB. Probable PCTB (in the absence of a positive pericardial fluid culture) will be defined as per Mayosi et al.4:

• Evidence of pericarditis with microbiologic confirmation of Mtb- infection elsewhere in the body and/or
• Exudative, lymphocyte predominant effusion with elevated adenosine deaminase (≥35 U/L)
• Participant will undergo pericardiocentesis (as per clinical indication)
• Within 5 days of ATT initiation

Критерии исключения

• Glomerular filtration rate <30ml/min or renal failure requiring dialysis
• Rifampin-resistant TB
• Severe concurrent opportunistic infection
• Contraindication to placement of intra-pericardial catheter
• Failed pericardiocentesis procedure and/or failure of placement of intra-pericardial catheter
• Any disease or condition in which the use of the standard anti-TB drugs (or any of their components) are contraindicated. This includes, but is not limited to, allergy to any TB drug or their components.
• In females: a positive urine pregnancy test result
• Confirmed autoimmune disorders (e.g. systemic lupus erythematosus)

Additional Exclusions for Gadolinium contrasted CMR

• Any implanted devices that are not MR compatible (e.g. pacemaker, defibrillators, cerebral aneurysm clips, cochlear implants etc.)
• Claustrophobia
• Gadolinium allergy
• Inability to lie on a flat surface for prolonged periods of time (e.g. severe congestive cardiac failure)
• Breastfeeding

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Тройное слепое

Основная цель

Фундаментальное исследование

Центры проведения

ЮАР · 2 центра

• Nelson Mandela Academic Hospital — Mthatha
• Groote Schuur Hospital — Cape Town

Идентификаторы

NCT: NCT04521803 · IMPI-3 DMID 20-0007

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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