Skip to content

Comparision of intrathecal morphine and continuous wound infiltration of local anesthetics

Comparision of low-dose intrathecal morphine and ropivacaine continuous wound infiltration for postoperative analgesia after living-donor kidney transplantation: a prospective randomized trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0000830
Enrollment
52
Registered
2013-08-23
Start date
2012-02-15
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

Medical Device : No premedication was given to any of the patients. All patients were anesthetized with the same anesthetic technique. Before the induction of anesthesia, in ITM with IV-PCA group, d
the location of the catheter was between deep muscle fascia and external oblique muscle at the lateral side of the abdomen. After closure of surgical wound, a bolus dose of 0.75% ropivacaine 10ml was
Acemedical, Korea). All patients were received a standard postoperative analgesic protocol of fentanyl via the IV-PCA
the regimen was 1500 µg g of fentanyl in normal saline 100 mL (15 µg g/mL) and programmed for bolus, lockout time, and basal rate of 1 mL, 15 minutes, and 1 mL/hour, respectively. Meperidine (50 mg)

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: aged between 18 - 60 years, undergoing LDKT in samsung medical center

Exclusion criteria

Exclusion criteria: Individuals were excluded from the study if they had a known allergy to any of the drugs used in this study. Additionally, patients with bleeding diathesis, neurologic dysfunction (preexisting lower limb neurological deficit), recent systemic or local infections, insufficient comprehension to use the PCA device, history of drug abuse, or being treated with opioids because of chronic pain were excluded from the study

Design outcomes

Primary

MeasureTime frame
Numeric rating scale at rest and when coughing

Secondary

MeasureTime frame
amount of opioid consumption, , and side effects such as sedation, nausea/vomiting, pruritus, and respiratory depression;postoperative pulmonary functional test (FVC, FEV1);sedation;nausea/vomiting;pruritus;respiratory depression

Countries

Korea, Republic of

Contacts

Public ContactJoo Hyum Jun

Samsung Medical Center

Outcome results

None listed

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