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ow Dose Dexmedetomidine as an alternative to narcotic pain-killers in daycare surgeries.

Phase 3
Conditions
Health Condition 1: C679- Malignant neoplasm of bladder, unspecified
Registration Number
CTRI/2019/02/017655
Lead Sponsor
Post Graduate Institute of Medical Education and research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.American Society of Anesthesiologists physical status I or II

2.Age of 18â??65 years

3.Either gender

4.Estimated operation time of <= 2 hours and anaesthesia time of <= 3 hours

5.Written informed consent to undergo the therapeutic regimen

Exclusion Criteria

1.Renal dysfunction (serum creatinine > 1.2mg/dl)

2.Liver dysfunction (liver enzymes twice the normal range or higher)

3.History of chronic use of sedatives/ narcotics or analgesics

4.BMI more than 30 kg/m2 or less than 15 kg/m2

5.Allergy to study medication

6.Participants devoid of postoperative telephone access

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to emergenceTimepoint: Time to emergence
Secondary Outcome Measures
NameTimeMethod
Secondary objectives: <br/ ><br>1.Predicted EC50 of propofol for induction <br/ ><br>2.Total propofol requirment for induction <br/ ><br>3. Intraoperative anaesthetic agent (MAC) requirement, <br/ ><br>4. Postoperative pain scores (VNRS) <br/ ><br>5. Perioperative analgesia requirements <br/ ><br>6. PONV <br/ ><br>7. Drowsiness (RASS score), <br/ ><br>8. Duration of PACU stay, <br/ ><br>9. Any adverse events. <br/ ><br>Timepoint: 120 minutes post intervention
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