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临床试验/CTRI/2024/05/068139
CTRI/2024/05/068139招募中3 期

Standard vs extended four-drugs for chemotherapy-induced nausea and vomiting prophylaxis in hematopoietic stem cell transplant (SENVIT): A phase III randomized control trial.

All India Institute of Medical Sciences New Delhi1 个研究点 分布在 1 个国家目标入组 198 人开始时间: 2024年6月14日最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
198
试验地点
1
主要终点
1A) Complete Response

研究概览

简要总结

This trial is to compare two prophylactic antiemetic regimens in the setting of hematopoietic stem cell transplant (HSCT)

Purpose: To compare the chemotherapy induced nausea and vomiting rates between standard 4 drugs vs extended 4 drugs in patients undergoing HSCT

Hypothesis: Extended 4 drugs improves the chemotherapy induced nausea and vomiting rate by at least 20% as compared to standard 4 drugs.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
12.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 12yrs- 65 yrs.
  • undergoing: a.
  • Conditioning for autologous hematopoietic stem cell transplant b.
  • Conditioning for allogenic hematopoietic stem cell transplant
  • Weight ≥ 30 kg.

排除标准

  • 未提供

结局指标

主要结局

1A) Complete Response

时间窗: From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.

Complete response (CR) was defined as absence of vomiting/ retching and no more than mild nausea during the specified phase.

时间窗: From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.

1B) Vomiting counts

时间窗: From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.

Number of vomiting episodes separated by at least 5 minutes of nausea and retching free interval

时间窗: From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.

次要结局

  • 2) Overall CR rates will be further subdivided into that for acute and delayed phase:
  • 3) Complete Protection(No nausea, no vomiting and no use of rescue medications for either nausea or vomiting.)
  • 4) Counts of rescue antiemetic doses defined as any therapy given in addition to the standard treatment, for uncontrolled retching/ vomiting, based on clinical judgement(From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.)
  • Individual toxicity episodes(From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.)
  • 6) Comparison of quality of life scores between the two arms(From initiation of conditioning to 6 days after the last dose of chemotherapy in the conditioning regimen.)

研究者

发起方
All India Institute of Medical Sciences New Delhi
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Debabrata Mohapatra

All India Institute of Medical Sciences

研究点 (1)

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