CTRI/2023/08/056100
Not Yet Recruiting
Phase 1
A randomised comparative study on postoperative analgesic efficacy of dexamethasone as and adjuvant to ropivacaine in incision site infilration in patients undergoing elective supratentorial craniotomy at S.M.S Medical College and Attached Group of Hospitals Jaipur. - Nil
SMS Medical College and attached Hospitals0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and Surgical
- Sponsor
- SMS Medical College and attached Hospitals
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients given informed and written consent
- •2\. 20 \- 50 years of age of either gender
- •3\. ASA physical status of I\-II
- •4\. Scheduled for elective supratentorial tumour craniotomy under general
- •anaesthesia
- •5\. Patients in whom surgeon anticipates uneventful extubation and return of
- •consciousness, orientation as well as cooperation after extubation so that patient may correctly express the degree of pain.
Exclusion Criteria
- •1\.Patients with history of previous craniotomy ,psychiatric disorders,epilepsy or chronic headaches
- •2\.BMI \<15 or \>35
- •3\. Allergic to opioids,dexamethasone or ropivacaine
- •4\.history of excessive alcohol or drug abuse
- •5\.preoperative GCS \<15
- •6\. Peri\-incisional infection
Outcomes
Primary Outcomes
Not specified
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