Search for Clinical Trial Results

Leishmaniasis - 70 Studies Found
Status | Study |
Completed |
Study Name: A Community Trial for Visceral Leishmaniasis (VL) Condition: Visceral Leishmaniasis Date: 2010-02-14 Interventions:
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Completed |
Study Name: Clinical Trial to Assess the Safety and Efficacy of Sodium Stibogluconate (SSG) and AmBisome® Combination, Miltefosine and AmBisome® and Miltefosine Alone for the Treatment Visceral Leishmaniasis in Eastern Africa Condition: Primary Visceral Leishmaniasis Date: 2010-02-10 Interventions:
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Completed |
Study Name: Efficacy, Acceptability and Cost-effectiveness of Long Lasting Insecticide Nets (LLIN) in the Prevention of Kala Azar Condition:
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Completed |
Study Name: Safety and Efficacy Study of Paromomycin to Treat Visceral Leishmaniasis Condition: Visceral Leishmaniasis Date: 2005-09-13 Interventions:
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Completed |
Study Name: Pharmacokinetics/Safety of Miltefosine Allometric Dose for the Treatment of Visceral Leishmaniasis in Children in Eastern Africa Condition: Visceral Leishmaniasis Date: 2015-04-20 Interventions: Drug: Miltefosine |
Not yet recruiting |
Study Name: Miltefosine/Paromomycin Phase III Trial for Treatment of Primary Visceral Leishmaniasis (VL) Patients in Eastern Africa Condition: Visceral Leishmaniasis Date: 2017-04-21 Interventions:
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Completed |
Study Name: Safety and Efficacy Study to Evaluate Different Combination Treatment Regimens for Visceral Leishmaniasis Condition: Visceral Leishmaniasis Date: 2008-06-11 Interventions:
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Completed |
Study Name: A Study to Explore Association of Treatment Regimens for Visceral Leishmaniasis, Host Immunological, Genetical and Nutrition Factors With Post-kala-azar Dermal Leishmaniasis (PKDL) Condition: Post-kala-azar Dermal Leishmaniasis Date: 2013-10-23 Interventions: Drug: Mitefosine Tablet Miltefosine 100 mg in two devided doses for 12 weeks |
Completed |
Study Name: Intralesional Voriconazole, or Intralesional Cryotherapy, or Oral Doxycycline in the Treatment of Cutaneous Leishmaniasis Condition: Leishmaniasis, Cutaneous Date: 2025-08-10 Interventions: Sessions will be held once weekly for a maximum of 6 weeks |
COMPLETED |
Study Name: Incidence of Relapse and Post-Kala-Azar Dermal Leishmaniasis in South Sudan Condition: Leishmaniasis Date: 2025-08-10 |