跳至主要内容
临床试验/CTRI/2020/02/023655
CTRI/2020/02/023655尚未招募不适用

Efficacy of dexmedetomidine and ketamine as an adjuvant with ropivacaine in PECS II block among the patients undergoing modified radical mastectomy/ breast conservation surgery: A Randomized double blind controlled trial

All india institute of medical sciences patna1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2020年2月29日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
75
试验地点
1
主要终点
To compare the total duration of post-operative analgesia and requirement of first rescue

研究概览

简要总结

This study is one of its kind as it is the study to compare the efficacy of drugs in controlling post operative analgesia among the patient undergoing breast surgeries using PECS 2 block  till date there are studies done in PECS 2 block but not with ropivacaine.since our study is mainly focused on comparing dexmeditomidine and ketamine along with ropivacaine by taking ropivacaine alone as a control group and to determine the requirement of rescue analgesia in 48 hours post operatively

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
Female

入选标准

  • Female population aged between 18-65 years 2) ASA I & II 3) Patients undergoing breast surgeries.

排除标准

  • Patient refusal Patients with underlying severe cardio-pulmonary compromise Morbid obesity BMI more than or equal to 35 Chest wall infiltration Presence of malignant breast mass in the field of block performance Pregnancy,lactation, dementia.
  • Allergy to Local Anesthetic or adjuvants, Patients already on prescribed oral opioid analgesics or psychotropic agents Post radiation status of breast or axilla.

结局指标

主要结局

To compare the total duration of post-operative analgesia and requirement of first rescue

时间窗: 48 hours

analgesia by the patient using an adjuvant (dexmedetomidine or ketamine) with ropivacaine in PEC II block undergoing breast surgeries

时间窗: 48 hours

次要结局

  • To determine the total amount of intra operative and post-operative opioid consumption(To assess the nnumerical rating scale in 1,2,4,6,1,18,24,48 hours post operatively)

研究者

发起方
All india institute of medical sciences patna
申办方类型
Research institution and hospital

研究点 (1)

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