The purpose of this study is to evaluate the effectiveness of treatment with PMIM in patients with visceral leishmaniasis within the VL-endemic region of Bangladesh at EOT (21/22 days after treatment begins), and at 6 months after end of treatment (Day 202/203, -15 to +30 days).
Safe, effective and affordable treatments for visceral leishmaniasis (VL) that are widely available to the poorest populations are urgently needed in Bangladesh in areas where the disease is endemic. Paromomycin IM Injection (PMIM) was approved for the treatment of VL in August 2006 by the Drugs Controller General of India (DCGI), and it offers an attractive alternative to treatments that are currently available.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
120
Paromomycin IM Injection, 11 mg/kg as the base, intramuscular, once a day on 21 consecutive days (or no more than 22 days if one injection is missed during the treatment period).
Bhaluka Upazila Health Complex
Bhaluka, Mymensingh District, Bangladesh
Trishal Upazila Health Complex
Trishal, Mymensingh District, Bangladesh
Icddr,B
Dhaka, Bangladesh
Final cure rate
Criteria evaluated (binary fashion): 1. Patient's temperature less than 99.4°F in clinic at EOT visit? (Y/N) 2. Patient reported resolution of fever and NO fever within the last 5 days? (Y/N) 3. Spleen size decreased from screening value? (Y/N) 4. Is the clinical impression of the treating physician that of an adequate clinical response? (Y/N) The patient is deemed to have achieved final cure if answers to a, b, c, AND d are all "Yes" OR if one answer (a, b, or c) is "No" but all others and "d" are "Yes". In addition, the clinician will inquire about pregnancy status for female patients.
Time frame: 6 months after end of treatment (Day 202/203, -15 to +30 days)
Initial clinical response rate
Criteria evaluated (binary fashion): 1. Patient's temperature less than 99.4°F in clinic at EOT visit? (Y/N) 2. Patient reported resolution of fever / NO fever within the last 5 days? (Y/N) 3. Spleen size decreased from screening value? (Y/N) 4. Is clinical impression of the treating physician that of an adequate clinical response? (Y/N) The patient is deemed to achieve an initial clinical response if answers to a, b, c, AND d are all "Yes" OR if one answer (a, b, or c) is "No" but all others and "d" are "Yes". Also, the clinician will inquire re: pregnancy status for female patients.
Time frame: End of treatment (21/22 days after treatment begins)
Patient compliance with PMIM treatment
Proportion of patients complying with prescribed 21 daily injections over no more than 22 days.
Time frame: 22 days
Safety of PMIM in the study population based on clinical assessment by the study physician at the Upazilla Health Centre.
All serious adverse events (SAEs), regardless of causality, from time of first administration of PMIM through 30 days post-EOT. All adverse events (AEs), regardless of causality, from time of first dose through 30 days post-EOT. Vital signs on Study Days 1 to 21/22 (or early termination), any unscheduled visit after EOT, 30 days after EOT, and 6 months after EOT. Patients who become pregnant during treatment/within 30d following EOT will be included in the safety population. Offspring from pregnancies will be followed for safety under a separate study for a period up to 3 yrs after birth.
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Time frame: 6 months after end of treatment
To introduce PMIM in government health facilities in rural Bangladesh.
Training study staff to provide treatment with PMIM at selected Upazila level health complexes in rural Bangladesh.
Time frame: October 2011