Bilateral superficial cervical plexus block for post-operative analgesia in thyroid surgeries using ropivacaine(0.2%) with or without dexmedetomidine

Phase 4

Recruiting

• Conditions: Disorder of thyroid, unspecified, (2) ICD-10 Condition: E079||Disorder of thyroid, unspecified,

• Registration Number: CTRI/2018/10/016018
• Lead Sponsor: MB hospital Udaipur

Brief Summary

To evaluate the effects of dexmedetomidine (1mcg/kg), adding to ropivacaine(0.2%)in bilateral superficial cervical plexus block  in thyroid  surgery  regarding effect on  :

Postoperative analgesia.

To determine the adverse effects, if any of ropivacaine and dexmedetomidine.

To study the post-operative pain management, rescue analgesic requirement, sedation in patients, hospital stay and patient comfort.

Detailed Description

Not available

Study Timeline

• Study Start: 2018-03-05
• Last Update Posted: 2019-03-07

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

the study conducted on 60 patients of ASA Grade I & II of either sex, aged 18 to 60 years, having a euthyroid state, who undergone elective thyroid surgeries under general anesthesia and after completion of surgery bilateral superficial cervical plexus block given.

Exclusion Criteria

patient refusal,age <18yrs, ASA grade >2,patient havong severe respiratory,cardiac or renal disorders,and acute psychiatric illness,infection at the injection site,allergy to agent used,morbid obesity (bmi>35),coagulation disorders.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative analgesia.	to study post-operative analgesia at 0hour,4hour,8hour,12hour and 24hour
To study the post-operative pain management, rescue analgesic requirement, sedation in patients, hospital stay and patient comfort.	to study post-operative analgesia at 0hour,4hour,8hour,12hour and 24hour
To determine the adverse effects, if any of ropivacaine and dexmedetomidine.	to study post-operative analgesia at 0hour,4hour,8hour,12hour and 24hour

Secondary Outcome Measures

Name	Time	Method
To study the post-operative pain management, rescue analgesic requirement, sedation in patients, hospital stay and patient comfort.	to study post-operative analgesia at 0hour,4hour,8hour,12hour and 24hour

Trial Locations

Locations (1)

Maharana Bhupal Hospital udaipur rajasthan; 🇮🇳 Udaipur, RAJASTHAN, India

Maharana Bhupal Hospital udaipur rajasthan

🇮🇳Udaipur, RAJASTHAN, India

Apoorva Aseri

Principal investigator

9460662200

aseriapoorva91@gmail.com