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临床试验/CTRI/2024/12/078007
CTRI/2024/12/078007尚未招募4 期

A comparison of postoperative analgesic efficacy between Dexmeditomidine with Levobupivacaine versus Dexmeditomidine with Ropivacaine in Ultrasound guided Transversus Abdominal block for total abdominal hysterectomy surgeries- A double blinded randomized controlled trial

M Madhubalan1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2024年12月25日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
62
试验地点
1
主要终点
The duration of Analgesia in post-operative period between the two groups. It will be measure with parameters such as VAS score , BLOOD PRESSUE , PULSE RATE .

研究概览

简要总结

COMPARISON OF POST OPERATIVE ANALGESIC EFFICACY BETWEEN DEXMEDETOMIDINE WITH LEVOBUPIVACAINE VERSUS DEXMEDITOMIDINE WITH ROPIVACAINE IN ULTRASOUND GUIDED TRANSVERSUS ABDOMINAL BLOCK FOR TOTAL ABDOMINAL HYSTERECTOMY SURGERIES

Primary objective:

The duration of Analgesia in post-operative period between the two groups.

Secondary objective:

To monitor heart rate, BP, SPO2 from the time of TAP block to the time of break through pain.

To monitor for complications, if any, from the time of tap block to the time of breakthrough pain .

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
Female

入选标准

  • Adult patients between 18 to 60 years of both sexes Patients belonging to ASA CLASS 1 to ASA CLASS 2 posted for elective lower abdominal hysterectomy surgeries Weight from 50 to 80 kgs.

排除标准

  • Patient refusal for regional anaesthesia.
  • Pregnancy and lactating female.
  • Obese patients.
  • Patience with ASA class three and four.
  • Patient is allergic to local anaesthetics and Dexmeditomidine.
  • Patients having any bleeding Coagulopathy disorders.

结局指标

主要结局

The duration of Analgesia in post-operative period between the two groups. It will be measure with parameters such as VAS score , BLOOD PRESSUE , PULSE RATE .

时间窗: Post operative day 0 to Post operative day 02

次要结局

  • To monitor heart rate, BLOOD PRESSURE, SPO2 , VAS SCORE from the time of TAP block to the time of break through pain.(To monitor for complications, if any, from the time of tap block to the time of breakthrough pain)

研究者

发起方
M Madhubalan
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Madhubalan Manivannan

Shri Sathya Sai Medical College and Research Institute

研究点 (1)

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