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临床试验/NCT05991466
NCT05991466已完成4 期

The Effect of Dexmedetomidine on the Quality of Recovery in Parturients Undergoing Elective Caesarean Sections: a Randomized Comparative Study

Cairo University1 个研究点 分布在 1 个国家目标入组 141 人开始时间: 2022年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
141
试验地点
1
主要终点
Quality of recovery score following CS (ObsQor-11) at the end of the first 24 hours postoperative.

研究概览

简要总结

The study hypothesizes that addition of dexmedetomidine to bupivacaine either in spinal anesthesia or TAP block is more effective and provide better ObsQor-11score than bupivacaine alone. Also, Dexmedetomidine in TAP block might provide a longer pain free time in comparison to intrathecal dexmedetomidine.

详细描述

Aim of the work To compare the quality of recovery (ObsQOR-11) in patients undergoing cesarean sections receiving dexmedetomedine either intrathecally or in the tap block in comparison to patients receiving conventional spinal anesthesia and tap block.

Statistical Analysis I. Sample size In a pilot study on 5 parturient who had undergone elective cesarean section under spinal anesthesia followed by TAP block with bupivacaine alone, the mean ObsQoR-11 at 24 hours was 65±9. In a single factor ANOVA study, sample size of 126 from the 3 groups is needed to detect a difference of at least 10 using the Tukey-Kramer (Pairwise) multiple comparison with study power of 83% and alpha error of 0.05. The common standard deviation within a group is assumed to be 9. The number of envelopes will be increased to 141 (47 per group) to compensate of possible 10% dropout. The sample size was calculated using PASS 15 Power Analysis and Sample Size Software (2017). NCSS, LLC. Kaysville, Utah, USA, ncss.com/software/pass.

II. Statistical analysis Data will be coded and entered using the statistical package SPSS (statistical package for the social science) version 22. Data will be summarized using mean, standard deviation, median, minimum and maximum in quantitative data and using frequency (count) and relative frequency(percentage)for categorical data. Comparisons between quantitative variables will be done using the non parametric Mann-Whitney test. For comparing categorical data, Chi square (x2 ) test will be performed. Exact test will be used instead when the expected frequency is less than 5. P-value less than 0.05 will be considered as statistically significant.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Participants will be full-term pregnant females
  • ASA classification I or ll.
  • Aged between 18 and 40 years.
  • Singleton pregnancy

排除标准

  • Refusal of block.
  • Bleeding disorders (platelets count <150,000; INR>1.5; PC<60%).
  • wounds or infection at the puncture site.
  • Known allergy to local anesthetic drugs.
  • Contraindications to neuroaxial block.
  • Contraindications to TAP block..

研究组 & 干预措施

Group(A)

Active Comparator

Spinal anaesthesia will be performed with 0.5% hyperbaric bupivacaine 10-12 mg and TAP block will be performed with 30 ml 0.25% bupivacaine in each side.

干预措施: Dexmedetomidine (Drug)

Group (B)

Active Comparator

Spinal anaesthesia will be performed with 0.5% hyperbaric bupivacaine10-12 mg and TAP block will be performed with 50 mcg Dexmedetomidine added to 30ml 0.25% bupivacaine in each side.

干预措施: Dexmedetomidine (Drug)

Group (C)

Active Comparator

Spinal anaesthesia will be performed with 0.5% hyperbaric bupivacaine 10-12 mg added to 5 mcg dexmedetomidine. TAP block will be performed with 30ml 0.25% bupivacaine in each side.

干预措施: Dexmedetomidine (Drug)

结局指标

主要结局

Quality of recovery score following CS (ObsQor-11) at the end of the first 24 hours postoperative.

时间窗: 24 hours postoperative

The mothers will be asked to rate each recovery item with an 11-point numerical Likert scale (0 = strongly negative; 10 = strongly positive).

次要结局

  • Time of first request of analgesia in hours(within 24 hours postoperative)
  • Onset of sensory block(Post spinal anesthesia up to 30 minutes)
  • Incidence of bradycardia(post spinal anesthesia up to 1 hour)
  • Incidence of hypotension(post spinal anesthesia up to 1 hour)
  • Neonatal Apgar score(at 1 and 5 minutes post delivery)
  • Intra operative non-invasive mean blood pressure(within 24 hours postoperative)
  • Complications of spinal anaesthesia and TAP block(12 hours post operative period.)
  • Ramsay sedation scale(1, 2, 4, 6, 8, 12 and 24 hours)
  • Intra operative heart rate(within 24 hours postoperative)
  • Visual Analogue Scale(1, 2, 4, 6, 8, 12 and 24 hours postoperative)
  • Onset of motor block using Bromage scale(Post spinal anesthesia up to 30 minutes)
  • Nausea and vomiting(intraoperative and postoperative 24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohamed Ahmed Mohamed Youssef Ollaek

Assistant Professor

Cairo University

研究点 (1)

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