A study of postoperative recovery between intravenous anesthesia group and inhalation anesthesia using sevoflurane group after hand assisted laparoscopic donor nephrectomy in living donors for kidney transplantation

Comparison of early postoperative recovery between propofol and sevoflurane anesthesia based on intrathecal morphine pain control in living kidney donors undergoing hand assisted laparoscopic nephrectomy: a prospective randomized study

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004351

Enrollment

Registered

2019-10-18

Start date

2019-10-18

Completion date

Unknown

Last updated

2020-02-24

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

Conditions

None listed

Interventions

Drug : One group of patients undergoing general anesthesia was given continuous IV (intravenous) infusion of propofol to the effect site concentration of 3 to 5 mcg/ml using TCI (target controlled inf

(1 MAC) of Sevoflurane via endotracheal tube until the end of the operation.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Healthy donors scheduled to undergo kidney donation at Seoul St. Mary's Hospital 2. Donors who can be administered intrathecal morphine 3. Adults (ages 19 years or older) 4. American Society of Anesthesiologists physical status 1 or 2 grade

Exclusion criteria

Exclusion criteria: 1. Patients who do not agree to participate in this study 2. Emergency surgery 3. Patient contraindicated for spinal puncture 4. Children (under 19 years old) 5. American Society of Anesthesiologists' physical status 3 or 4 grade 6. Intraoperative bleeding requires colloid or transfusion during surgery 7. Hemodynamic instability to the extent that vasoactive drugs are necessary.

Design outcomes

Primary

Measure	Time frame
Result of quality of recovery-40 questionnaire for 24 hours after the operation	—

Secondary

Measure	Time frame
Total number of steps for 24 hours after operation;Availability of early ambulation on the day of the operation;Complications occurs for 24 hours after the operation;Total dose of IV PCA infused for 6 hours and 24 hours after the operation;Availability of ambulation on the day after the operation;Frequency and amount of acute pain control medicine administered for 24 hours after the operation;Blood test results preoperative and 6 hours, 24 hours after the operation;Clavien-Dindo surgical complication grade;Todal hospital stay	—

Measure

Time frame

Total number of steps for 24 hours after operation;Availability of early ambulation on the day of the operation;Complications occurs for 24 hours after the operation;Total dose of IV PCA infused for 6 hours and 24 hours after the operation;Availability of ambulation on the day after the operation;Frequency and amount of acute pain control medicine administered for 24 hours after the operation;Blood test results preoperative and 6 hours, 24 hours after the operation;Clavien-Dindo surgical complication grade;Todal hospital stay

—

Countries

Korea, Republic of

Contacts

Public ContactMinsuk Chae

The Catholic University of Korea, Seoul St. Mary's Hospital

Outcome results