跳至主要内容
临床试验/CTRI/2021/01/030835
CTRI/2021/01/030835尚未招募不适用

Effect of lignocaine spray in addition to paracervical block as analgesia for uterine curretage- An observational study

Mahatma Gandhi Medical College and research Institute1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年1月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
To compare the effect of lignocaine spray plus paracervical block with paracervical block alone for pain relief by

研究概览

简要总结

Patients fulfilling the eligibilty criteria will be included after obtaining informed  consent. Detailed history, clinical examination and routine preoperative investigation will be done and patients will be allocated into group 1 and group 2.In Group 1 patients 10ml of 1% lignocaine will be injected paracervically at 5 and 7 o’ clock at the junction of cervix and vagina for Paracervical block(PCB). In Group 2 patients,3 puffs of lignocaine spray(30mg of 10% lignocaine) will be directed on cervix and vaginal vault. After a waiting period of 2 minutes cervix will be held with  an instrument and another 3 puffs will be directed towards the cervical external os. After further waiting period of 2 minutes 10ml of lignocaine will be injected paracervically at 5 and 7 o’clock at the junction of cervix and vagina for PCB .After PCB patients will undergo uterine curettage procedures according to the institution protocol. Pain score will be qualified by numeric pain rating scale(NPRS) which will be explained to the patient before the procedure. NPRS will be used after holding the cervix, immediately after the procedure,30 minutes and 1 hour after the procedure.

研究设计

研究类型
Interventional
分配方式
Other

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
Female

入选标准

  • Patients planned for uterine curettage procedure under paracervical block.

排除标准

  • Hypersensitivity to lignocaine Active genital tract infection Past history of cervical surgery History of chronic pelvic pain.

结局指标

主要结局

To compare the effect of lignocaine spray plus paracervical block with paracervical block alone for pain relief by

时间窗: Till 1 hour post procedure

immediately after procedure

时间窗: Till 1 hour post procedure

after holding the cervix with instrument

时间窗: Till 1 hour post procedure

30 minutes post procedure

时间窗: Till 1 hour post procedure

1 hour post procedure

时间窗: Till 1 hour post procedure

次要结局

  • Side effects between the 2 groups(Compare satisfaction score between the 2 groups using 5 point likert scale)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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