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Effect of Block of nerves supplying scalp with drug levobupivacaine and ketamine versus levobupivacaine only on requirement of opioid medicines during and after operation in Patients having brain tumour operations

Phase 3
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/02/062724
Lead Sponsor
All India Institute of Medical Sciences, Bathinda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients between 18-70 years of age

2.Patients scheduled for elective supratentorial craniotomy, belonging to American Society of Anaesthesiologists (ASA) physical status I, II, or III.

3.Patients undergoing intraoperative pin fixation of the head.

4.Preoperative GCS 15

5.Patients with an anticipated full awakening from general anaesthesia within 2 hours postoperatively.

Exclusion Criteria

1.History of craniotomy with absent bone flap

2.Frontal craniotomy

3. Known psychiatric disorder

4. Uncontrolled epilepsy

5.Chronic headache.

6. Peri-incisional infection

7. No plan to extubate or expected prolonged mechanical ventilation.

8.Known allergy to NSAIDS, ketamine, or levobupivacaine.

9. Chronic opioid use ( >2 weeks) or history of excessive alcohol or drug abuse

10. Inability to understand the use of NRS.

11. Extremes of body mass index (BMI) ( <15 or >35 kg/cm2).

12. Pregnant or breastfeeding.

Withdrawal criteria

1.Not awake 2 hours after surgery.

2.Early revision within the first 48 hours.

3.Voluntary withdrawal.

4.Received radiation therapy and chemotherapy postoperatively.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome of our study will be time of first rescue analgesic administration from the time of test drug administration recorded as the pain-free interval. <br/ ><br>Timepoint: pain-free interval to be assessed <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Cumulative dose of intraoperative opioids.Timepoint: duration of anesthesia;Cumulative dose of rescue analgesic requirement in the first 24 hours and 48 hours postoperative period.Timepoint: 24 hours postoperative period <br/ ><br>48 hours postoperative period.;Postoperative nausea and vomiting (PONV) assessed at 2, 4, 8, 24, and 48 hours after surgeryTimepoint: 2, 4, 8, 24, and 48 hours after surgery;Postoperative pain scores assessed by NRS. The NRS scores will be recorded at 2, 4, 8, 12, 16, 20, 24, 36, and 48 h after surgery.Timepoint: 2, 4, 8, 12, 16, 20, 24, 36, and 48 h after surgery;Ramsay Sedation ScaleTimepoint: 2,4,8,24 and 48 hours after surgery
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