Target controlled infusion for propofol anesthesia during Transjugular Intrahepatic Porto Systemic Shunt procedure

Target controlled infusion for propofol anesthesia during Transjugular Intrahepatic Porto Systemic Shunt procedure: a randomized controlled trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202310626983365

Enrollment

Registered

2023-10-19

Start date

2023-07-01

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaesthesia

Interventions

target controlled infusion

control group

Eligibility

Sex/Gender

All

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
compare sedline reading and level of sedation in TIPS between the groups	—

Secondary

Measure	Time frame
To evaluate the recovery time, profile, total propofol consumption, with recording the patient and interventional radiologist satisfaction.	—

Countries

Egypt

Contacts

Public Contacthanaa rashed

lecturer of anasthesia

hanaarashed2020@yahoo.com0248986754

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026