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Effects of Pre-emptive Scalp Infiltration With Low-dose Ketorolac and Ropivacaine for Postoperative Pain — PAINLESS  

Pain Clinical Trial

Official title:
Effects of Pre-emptive Scalp Infiltration With Low-dose Ketorolac and Ropivacaine for Postoperative Pain Relief After Elective Supratentorial Craniotomy (PAINLESS): a Randomized Controlled Pilot Trial

Clinical Trial Summary

The PAINLESS study is a single-center, prospective, randomized, open-label, blinded-endpoint (PROBE) controlled clinical pilot study to compare the efficacy and safety of pre-emptive scalp infiltration with ropivacaine plus ketorolac and ropivacaine alone for postoperative pain relief in adults undergoing elective supratentorial craniotomies.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04380298
Study type Interventional
Source Beijing Tiantan Hospital
Contact Fang Luo, M.D
Phone +8613611326978
Email 13611326978@163.com
Status Not yet recruiting
Phase Phase 4
Start date December 1, 2020
Completion date August 31, 2021
View Details
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