跳至主要内容
临床试验/TCTR20210927003
TCTR20210927003招募中不适用

The Prevalence of HIV Elite Controllers, Viremic Controllers, False Elite Controllers, and False Viremic Controllers in Thai Blood Donors

Faculty of Medicine, Chulalongkorn University0 个研究点目标入组 93 人开始时间: 2021年9月27日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
93

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
N/A (No limit) 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. HIV Ag/Ab reactive (positive 3 times) or inconclusive (positive 2 times)
  • 2. HIV NAT negative

排除标准

  • 1. HIV Ag/Ab negative the first time or positive only 1 time from 3 times
  • 2. HIV NAT positive

研究者

相似试验

招募中
4 期
A clinical trial to study the effects of fixed dose combination of Metoprolol and Telmisartan (Metosartan) in patients with essential hypertensio
CTRI/2022/09/045464Sun Pharma Laboratories Limited SP
进行中(未招募)
1 期
A Phase IV, Single-Centre, Observer-Blind, Controlled, Randomized Study to Compare the Safety and Immunogenicity of Fluvirin® to Influvac® Administered to Healthy Children 3 to 12 Years of Age. - Fluvirin Paediatric Trial
EUCTR2006-002649-35-GBovartis Vaccines and Diagnostics S.r.l.
尚未招募
3 期
A RANDOMIZED, OPEN-LABEL, C5 INHIBITOR-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF POZELIMAB AND CEMDISIRAN COMBINATION THERAPY IN PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA WHO ARE COMPLEMENT INHIBITOR TREATMENT-NAIVE OR HAVE NOT RECENTLY RECEIVED COMPLEMENT INHIBITOR THERAPYD599 Acquired haemolytic anaemia, unspecifiedAcquired haemolytic anaemia, unspecifiedD599
PER-036-23REGENERON PHARMACEUTICALS, INC.
进行中(未招募)
不适用
Multicenter, Phase IV, Open-Label, Uncontrolled Study to Assess the Efficacy and Safety of a Single Intravenous Dose of Palonosetron 0.25 mg (Aloxi®, Onicit®, Paloxi®) in the Prevention of Chemotherapy-Induced Nausea and Vomiting in Patients with Non-Hodgkin’s Lymphomas Undergoing Repeated Cycles of Moderately Emetogenic ChemotherapyPrevention of moderately emetogenic CINV in up to four repeated and consecutive single-day MEC cycles administered to patients with Non-Hodgkin’s Lymphomas.MedDRA version: 13.1Level: PTClassification code 10054133Term: Prophylaxis of nausea and vomitingSystem Organ Class: 10042613 - Surgical and medical procedures
EUCTR2008-007827-14-DEHelsinn Healthcare SA200
进行中(未招募)
不适用
Multicenter, Phase IV, Open-Label, Uncontrolled Study to Assess the Efficacy and Safety of a Single Intravenous Dose of Palonosetron 0.25 mg (Aloxi®, Onicit®, Paloxi®) in the Prevention of Chemotherapy-Induced Nausea and Vomiting in Patients with Non-Hodgkin’s Lymphomas Undergoing Repeated Cycles of Moderately Emetogenic ChemotherapyPrevention of moderately emetogenic CINV in up to four repeated and consecutive single-day MEC cycles administered to patients with Non-Hodgkin’s Lymphomas.MedDRA version: 12.0Level: LLTClassification code 10054133Term: Prophylaxis of nausea and vomiting
EUCTR2008-007827-14-CZHelsinn Healthcare SA200