| Unique ID issued by UMIN | UMIN000060238 |
|---|---|
| Receipt number | R000067591 |
| Scientific Title | Double-Blind Randomized Controlled Trial to Determine the Efficacy of Intraoperative Sacral Epidural Block for Postoperative Pain Control in Microsurgical Spinal Decompression for Lumbar Spinal Stenosis |
| Date of disclosure of the study information | 2026/01/10 |
| Last modified on | 2025/12/30 15:35:13 |
Caudal Epidural Block with Morphin for Postoperative Analgesia in LSS
EBM-PAinLeSS study
Double-Blind Randomized Controlled Trial to Determine the Efficacy of Intraoperative Sacral Epidural Block for Postoperative Pain Control in Microsurgical Spinal Decompression for Lumbar Spinal Stenosis
EBM-PAinLeSS study
| Japan |
Lumbar Spinal Stenosis
| Orthopedics | Neurosurgery |
Others
NO
To clarify the efficacy of a single-dose sacral epidural block using morphine hydrochloride and ropivacaine administered intraoperatively (immediately before skin incision after general anesthesia) during microsurgical spinal canal enlargement for spinal canal stenosis in controlling postoperative pain.
Safety,Efficacy
1 Percentage of patients who did not require analgesics within 48 hours after extubation
2 Time from extubation to administration of rescue analgesics in patients who required them
1 Total intraoperative opioid analgesic administration excluding epidural preoperative administration
2 Post-extubation pain scale
3 Post-extubation pruritus scale
4 Postoperative nausea and vomiting scale
Interventional
Parallel
Randomized
Cluster
Double blind -all involved are blinded
Placebo
YES
NO
Institution is not considered as adjustment factor.
YES
Central registration
2
Treatment
| Medicine |
Drug administration group:
Sacral epidural block using a mixture of 5mg/0.5ml morphine hydrochloride and 19.5ml saline solution (20ml total)
One shot administered immediately before surgery
Placebo group:
20 ml saline solution administered via sacral epidural injection
One shot administered immediately before surgery
| 50 | years-old | <= |
| 85 | years-old | >= |
Male and Female
1. Patients undergoing microscopic spinal decompression for one or two intervertebral segments lumbar spinal stenosis between the third lumbar vertebra and the first sacral vertebra
2. American Society of Anesthesiologists (ASA) physical status grade 2 or lower
1. Planned reoperation cases, reoperation cases for adjacent segment disorders following prior surgery
2. Emergency surgery cases
3. Lumbar spinal stenosis cases due to spinal or spinal cord tumors
4. Cases with spinal infections, including spinal tuberculosis
5. Lumbar spinal stenosis cases associated with vertebral fractures
6. Cases receiving preoperative opioid administration
7. Cases with a history of hypersensitivity to water-soluble morphine
72
| 1st name | Naokado |
| Middle name | |
| Last name | Ikeda |
Ijinkai Takeda General Hospital
Department of Neurosurgery
601-1495
28-1 Ishidamori minami-cho, Fushimi-Ku, Kyoto
+81-75-572-6331
naokado.ikeda@ompu.ac.jp
| 1st name | Kunio |
| Middle name | |
| Last name | Yokoyama |
Ijinkai Takeda General Hospital
Department of Neurosurgery
601-1495
28-1 Ishidamori minami-cho, Fushimi-Ku, Kyoto
+81-75-572-6331
https://www.takedahp.or.jp/ijinkai/cooperation/clinical_research/
kunio.yokoyama@ompu.ac.jp
Ijinkai Takeda General Hospital
none
Other
Ijinkai Takeda General Hospital, Clinical Research Center
28-1 Ishidamori minami-cho, Fushimi-ku, Kyoto
+81-75-572-6331
mtsnaruse@nifty.com
NO
医仁会武田総合病院 (京都府)
| 2026 | Year | 01 | Month | 10 | Day |
Unpublished
Enrolling by invitation
| 2025 | Year | 12 | Month | 01 | Day |
| 2025 | Year | 12 | Month | 09 | Day |
| 2026 | Year | 01 | Month | 15 | Day |
| 2028 | Year | 12 | Month | 31 | Day |
| 2025 | Year | 12 | Month | 30 | Day |
| 2025 | Year | 12 | Month | 30 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000067591