Comparison of non-opioid pain control protocol using regional anesthesia and pain control using opioid in postoperative pain control

Multimodal analgesic protocol using pudendal nerve block and quadratus lumborum block on pain management after robot-assisted radical prostatectomy : a randomized open label , non-inferior trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0003589

Enrollment

Registered

2019-03-06

Start date

2019-02-25

Completion date

Unknown

Last updated

2019-03-25

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

Conditions

None listed

Interventions

Drug, Procedure/Surgery : Non-opioid pain control protocol group: 1. Patient takes pregalbaline 150mg orally 2h before surgery 2. Just after induction of general anesthesia: Bilateral quadratus lumb

ropivacaine 25cc and bilateral pudendal nerve block using 0.2&#37

5cc are perfomed before skin incision 3. Patietns receives propacetamol 1.0g intravenously before skin incision and every 8 hour duing 48 h after end of surgery. 4. Patients receives tramadol 50mg

5). Opioid pain control group: 1. After the end of surgery, patient controlled analgesia devcie (a self-paced, self-injecting device, bolus only mode, morphine 1mg, rock-out time 5 min) is connect

s intravenous line to control postoperative pain by him- or herself. 2. Patients receives tramadol 50mg intravenously if patietns complain sevever pain (NRS pain &gt

5).

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: 1) Patients scheduled to undergo laparoscopic colectomy at Kyungpook National University Chilgok Hospital 2) Patinetns who are 20-75 years old. 3) Patients who graded as American Society of Anesthesiologists Physical Status I or II 4) Patients whose main skin incision length is expected to be less than 6 cm 5) Patients with bilirubin levels below 0.4 mg / dl 6) Patients with glomerular filtration rate over 50cc / min

Exclusion criteria

Exclusion criteria: 1) Patients with allergies to morphine, pregabalin, ropivacaine 2) Patients with drug dependence 3) Patients with chronic pain 4) Patients with sleep apnea 5) Patients with asthma or chronic obstructive pulmonary disease 6) Patiens who take analgesics within 24 hours before surgery 7) Patients with mental illness

Design outcomes

Primary

Measure	Time frame
Pain score	—

Secondary

Measure	Time frame
Postoeprative nausea and vomitting;Discormport due to unrinary catheter	—

Countries

Korea, Republic of

Contacts

Public ContactJinseok Yeo

Kyungpook National University Medical Center

painfree@gmail.com+82-53-200-2644

Outcome results