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临床试验/PACTR202210622254726
PACTR202210622254726尚未招募3 期

RECTAL VERSUS INTRAMUSCULAR DICLOFENAC SODIUM FOR PAIN RELIEF AFTER CAESAREAN SECTION: A SINGLE BLIND RANDOMISED CONTROL STUDY

DR UGWU PAULINUS CHUKWUEMEKA0 个研究点目标入组 242 人开始时间: 2022年10月9日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
242

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Booked participants for elective or emergency lower segment caesarean delivery under spinal anaesthesia.

排除标准

  • 1. Participants booked for caesarean delivery under general anaesthesia.
  • 2. Participants with medical condition known to be potentially exacerbated by non-steroidal anti-inflammatory drugs such as peptic ulcer disease.
  • 3. Participants with previous history of adverse reaction or hypersensitivity to diclofenac or pentazocin.
  • 4. Participants who require special post-operative pain control such as sickle cell disease patient.
  • 5. Participant with known renal disease.
  • 6. Participants with known liver disease.

研究者

发起方
DR UGWU PAULINUS CHUKWUEMEKA

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