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Comparison of patient-controlled analgesia for laparoscopic radical prostatectomy surgery

Comparison of patient-controlled epidural analgesia with patient-controlled intravenous analgesia for laparoscopic radical prostatectomy surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002245
Enrollment
40
Registered
2017-02-27
Start date
2016-07-14
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Pusan National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 40 patients who are ASA(American Society of Anesthesiologist) I or II were included. Patients, aged 45 to 75 years old, who were scheduled for laparoscopic radical prostatectomy were included.

Exclusion criteria

Exclusion criteria: Patients who do not qualify for treatment of opioids, NSAIDs and epidural procedure, or who have psychological disorder, chronic pain disorder, renal failure, hepatic failure or preoperative administration of drugs including opioids, antidepressants, gabapentin, pregabalin, and carbamazepine, were excluded.

Design outcomes

Primary

MeasureTime frame
Numeric rating scale—

Secondary

MeasureTime frame
administered analgesic arug and muscle relaxant;side-effects after the operation;admission day;satisfaction of surgeon and patients;vital sign during the operation—

Countries

Korea, Republic of

Contacts

Public ContactBoo young Hwang

Pusan National University Hospital

love840108@hanmail.net+82-51-240-7399

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026