Target controlled infusion for propofol anesthesia during Transjugular Intrahepatic Porto Systemic Shunt procedure
Phase 4
Recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR202310626983365
- Lead Sponsor
- natioanl liver institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 78
Inclusion Criteria
1. Patients from 18 to 60 years from both sex.
2. Patients with American Society of Anesthesia ASA
classification II.
3. Patients candidate for TIPS intervention
Exclusion Criteria
Patients with uncontrolled cardiovascular, respiratory or
renal dysfunction.
2. History of allergy to any used anesthetic agent.
3. Morbid obesity with body mass index(BMI =40 Kg/m2).
4. Perioperative significant bleeding or hemodynamic
instability (e.g Air embolism) will be excluded from the
study.
5. Patient refusal to participate in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method compare sedline reading and level of sedation in TIPS between the groups
- Secondary Outcome Measures
Name Time Method To evaluate the recovery time, profile, total propofol<br>consumption, with recording the patient and interventional<br>radiologist satisfaction.